TRR
{

RETE|ID 1 FBtr0000018	SYM 1 Ecol\lacZ<up>per.P</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 1786
ID|FBtr0000018
SYM|Ecol\lacZ<up>per.P</up>RA
SYN|lacZ<up>per.P</up>RA
ASAL|<fbsym>FBal0041828==Ecol\lacZ<up>per.P</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000019
ASTP|<fbsym>FBtp0004424==P{lacZ<up>per.P</up>}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0056576
|Ewer et al.
|1992
RNAT|mRNA
BODP|A detailed examination of the distribution of <fbsym>FBal0041828==Ecol\lacZ[per.P]</fbsym> expressing
| cells within the adult brain was made. Expression was detected in the
| ocelli, the photoreceptor cells, and throughout the central brain and the
| optic ganglia. The detailed locations of expressing cells were described.
| The <fbsym>FBgn0014447==Ecol\lacZ</fbsym> distribution pattern matches the pattern of <fbsym>FBgn0003068==per</fbsym> protein
| expression qualitatively but the relative expression levels in different
| cells does not always correspond. Double staining with an antibody to
| <fbsym>FBgn0000570==elav</fbsym> which recognizes only neurons was used to determine the nature of
| the <fbsym>FBal0041828==Ecol\lacZ[per.P]</fbsym> staining cells. The cells in the ocelli and eyes,
| the lateral cells, and the dorsalmost cortex cells were shown to be
| neurons. The staining cells located at the margins of the cortex and
| neuropil in the optic lobes and the central brain, the cells within the
| lamina and central brain neuropil, and the cells in the inner chiasm are
| not neurons and are thought to be glia.
ASM|transcript distribution deduced from reporter protein
CVBODP|<t> A <a> ocellus <p>
|<t> A <a> photoreceptor cell <p>
|<t> A <a> lamina neuropil <p>
|<t> A <a> neuropil <p>
|<t> A <a> supraoesophageal ganglion <p>
|<t> A <a> optic lobe  <p>
|<t> A <a> optic chiasma  <p>
}

REF
{
REFM|FBrf0056576
|Ewer et al.
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000021	SYM 1 slo<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 424
ID|FBtr0000021
SYM|slo<up>+</up>RA
ASAL|<fbsym>FBal0071066==slo<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000022
ASGN|<fbsym>FBgn0003429==slo</fbsym>
ASPP|<fbsym>FBpp0001269==slo<up>+</up>P1175</fbsym>

REFDSR
{
RDID|FBrf0057357
|Adelman et al.
|1992
RNAT|mRNA
CC|A complete cDNA was constructed and checked by sequencing (see
| <fbsym>slo[A1C2E2G5I0]</fbsym>).
}

REF
{
REFM|FBrf0057357
|Adelman et al.
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000022	SYM 1 slo<up>+</up>RB	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 424
ID|FBtr0000022
SYM|slo<up>+</up>RB
ASAL|<fbsym>FBal0071066==slo<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000023
ASGN|<fbsym>FBgn0003429==slo</fbsym>
ASPP|<fbsym>FBpp0001569==slo<up>+</up>P1166</fbsym>

REFDSR
{
RDID|FBrf0057357
|Adelman et al.
|1992
RNAT|mRNA
CC|A complete cDNA was constructed and checked by sequencing (see
| <fbsym>slo[A1C2E1G3I0]</fbsym>).
}

REF
{
REFM|FBrf0057357
|Adelman et al.
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000039	SYM 1 Dl<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 3	DT 1 6 Jan 2000	RESZ 4068
ID|FBtr0000039
SYM|Dl<up>+</up>R
ASAL|<fbsym>FBal0066914==Dl<up>+</up></fbsym>
DT|6 Jan 2000
|10 Mar 1998
ID2|FBtr0000040
ASGN|<fbsym>FBgn0000463==Dl</fbsym>

REFDSR
{
RDID|FBrf0051592
|Haenlin et al.
|1990
RNAT|mRNA
BODP|<fbsym>FBgn0000463==Dl</fbsym> transcripts are diffusely distributed throughout the embryo in stage 4.
| During stages 5 and 6, a gap-gene like pattern of expression is seen in
| four lateral zones that are ventrally connected by a continuous
| longitudinal band. In stage 7, a pair-rule-like pattern is observed. In
| stage 8, <fbsym>FBgn0000463==Dl</fbsym> transcripts are distributed diffusely in the neurogenic
| region on the trunk and head. In stage 9, all neurectodermal cells contain
| <fbsym>FBgn0000463==Dl</fbsym> transcripts. Expression in cell clusters within the neurectoderm is
| seen as long as neuroblast segregation is going on (until mid stage 11). At
| the same time a metameric pattern of expression is seen in the ectoderm
| with 14 stripes of expression. <fbsym>FBgn0000463==Dl</fbsym> transcripts are also present at high
| levels in neuroblasts in stages 11 and 12. From stage 10, transcripts are
| present in midline precursor cells. From stage 11, they are detected in
| developing sensory organs. From early stage 12, labelling is seen in the
| anlage of the stomatogastric nervous system and the optic lobe anlage.
| Strong expression is observed in the posterior midgut in stages 11 and 12
| and in the hindgut from the blastoderm until the organ differentiates.
| Labelling is seen in the tracheal tree from stage 13 onwards.
ASM|northern blot
CVBODP|in situ
|<t> E | stage 5,6 <a>  <p> 65-85% egg length
|<t> E | stage 5,6 <a>  <p> 40-65% egg length
|<t> E | stage 5,6 <a>  <p> 20-35% egg length
|<t> E | stage 5,6 <a>  <p> 5-15% egg length
|<t> E | stage 7 <a>  <p> pair rule
|<t> E | stage 8-11 <a> neurectoderm <p>
|<t> E | stage 9-11 <a> ectoderm <p>
|<t> E | stage 11,12 <a> neuroblast <p>
|<t> E | stage >=10 <a> ventral midline | precursor <p>
|<t> E | stage >=11 <a> embryonic peripheral nervous system <p>
|<t> E | stage >=12 <a> embryonic stomatogastric nervous system <p>
|<t> E | stage >=12 <a> procephalic neurogenic region <p>
|<t> E | stage 11,12 <a> posterior embryonic/larval midgut <p>
|<t> E | stage 4-13 <a> hindgut primordium <p>
|<t> E | stage >=13 <a> embryonic/larval tracheal system <p>
}

REFDSR
{
RDID|FBrf0056444
|Kopczynski and Muskavitch
|1992
RNAT|snRNA
CC|The minor <fbsym>FBgn0000463==Dl</fbsym> RNAs were shown to be composed of intronic sequences. Introns
| excised from <fbsym>FBgn0000463==Dl</fbsym> primary transcripts accumulate to unusually high levels
| in embryos and were shown by high resolution in situ hybridizations to
| localize to 2 foci per embryonic nucleus.
}

REFDSR
{
RDID|FBrf0080309
|Parks et al.
|1995
RNAT|mRNA
BODP|<fbsym>FBgn0000463==Dl</fbsym> intron probes were used to assay <fbsym>FBgn0000463==Dl</fbsym> transcription in the eye.
| Transcripts are observed in nearly all cells in the morphogenetic furrow. A
| pattern begins to emerge posterior to the furrow as clusters are just
| beginning to rotate. Transcription is first seen in R3 and R4 and is
| stronger in R3 in early clusters. In subsequent rows, transcription in R1
| and R6 is observed. By row 7 or 8, transcription is stronger in R4 than R3,
| continues in R1 and R6 and is first seen in R7. By row 8 or 9, <fbsym>FBgn0000463==Dl</fbsym>
| transcription is found only in R4 and R7 and by row 14, <fbsym>FBgn0000463==Dl</fbsym> transcription
| has ceased in photoreceptors.
ASM|in situ
CVBODP|in situ
|<t> L | third instar <a> photoreceptor cell R3 <p>
|<t> L | third instar <a> photoreceptor cell R4 <p>
|<t> L | third instar <a> photoreceptor cell R1 <p>
|<t> L | third instar <a> photoreceptor cell R6 <p>
|<t> L | third instar <a> photoreceptor cellR7 <p>
|<t> L | third instar <a> morphogenetic furrow <p>
|<t> L | third instar <a> eye disc <p>
}

REF
{
REFM|FBrf0051592
|Haenlin et al.
|1990
REFM|FBrf0056444
|Kopczynski and Muskavitch
|1992
REFM|FBrf0080309
|Parks et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000062	SYM 1 Ecol\lacZ<up>Ubx.pbxPSc</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 488
ID|FBtr0000062
SYM|Ecol\lacZ<up>Ubx.pbxPSc</up>RA
SYN|lacZ<up>Ubx.pbxPSc</up>RA
ASAL|<fbsym>FBal0042201==Ecol\lacZ<up>Ubx.pbxPSc</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000063
ASTP|<fbsym>FBtp0004630==P{lacZ<up>Ubx.pbxPSc</up>}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0055958
|Muller and Bienz
|1992
RNAT|mRNA
BODP|No expression detected
ASM|transcript distribution deduced from reporter protein
}

REF
{
REFM|FBrf0055958
|Muller and Bienz
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000065	SYM 1 Ecol\lacZ<up>Ubx.pbxPSd</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 608
ID|FBtr0000065
SYM|Ecol\lacZ<up>Ubx.pbxPSd</up>RA
SYN|lacZ<up>Ubx.pbxPSd</up>RA
ASAL|<fbsym>FBal0042202==Ecol\lacZ<up>Ubx.pbxPSd</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000066
ASTP|<fbsym>FBtp0004631==P{lacZ<up>Ubx.pbxPSd</up>}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0055958
|Muller and Bienz
|1992
RNAT|mRNA
BODP|A <fbsym>FBgn0001077==ftz</fbsym>-like stripe pattern was observed in parasegments 6 and 8.
ASM|transcript distribution deduced from reporter protein
CVBODP|<t> E <a> parasegment 6,8 <of> ectoderm <p>
}

REF
{
REFM|FBrf0055958
|Muller and Bienz
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000066	SYM 1 Ecol\lacZ<up>Ubx.pbxPS</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 731
ID|FBtr0000066
SYM|Ecol\lacZ<up>Ubx.pbxPS</up>RA
SYN|lacZ<up>Ubx.pbxPS</up>RA
ASAL|<fbsym>FBal0042200==Ecol\lacZ<up>Ubx.pbxPS</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000067
ASTP|<fbsym>FBtp0004629==P{lacZ<up>Ubx.pbxPS</up>}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0055958
|Muller and Bienz
|1992
RNAT|mRNA
BODP|The reporter construct is expressed in a broad band in the posterior half of
| the blastoderm embryo from 15-45% egg length and weakly in ectodermal
| stripes in even numbered parasegments 6 and 8 after gastrulation.
ASM|transcript distribution deduced from reporter protein
CVBODP|<t> E | blastoderm <a>  <p> 15-45% egg length
}

REF
{
REFM|FBrf0055958
|Muller and Bienz
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000068	SYM 1 Ecol\lacZ<up>Ubx.pbxPP</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 597
ID|FBtr0000068
SYM|Ecol\lacZ<up>Ubx.pbxPP</up>RA
SYN|lacZ<up>Ubx.pbxPP</up>RA
ASAL|<fbsym>FBal0042197==Ecol\lacZ<up>Ubx.pbxPP</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000069
ASTP|<fbsym>FBtp0004626==P{lacZ<up>Ubx.pbxPP</up>}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0055958
|Muller and Bienz
|1992
RNAT|mRNA
BODP|The reporter construct is expressed weakly in "ftz-like" ectodermal stripes
| in even numbered parasegments 6 and 8 after gastrulation.
ASM|transcript distribution deduced from reporter protein
}

REF
{
REFM|FBrf0055958
|Muller and Bienz
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000069	SYM 1 Ecol\lacZ<up>Ubx.pbxPPb</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 663
ID|FBtr0000069
SYM|Ecol\lacZ<up>Ubx.pbxPPb</up>RA
SYN|lacZ<up>Ubx.pbxPPb</up>RA
ASAL|<fbsym>FBal0042199==Ecol\lacZ<up>Ubx.pbxPPb</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000070
ASTP|<fbsym>FBtp0004628==P{lacZ<up>Ubx.pbxPPb</up>}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0055958
|Muller and Bienz
|1992
RNAT|mRNA
BODP|The reporter construct is expressed weakly in "ftz-like" ectodermal stripes
| in even numbered parasegments 6 and 8 after gastrulation.
ASM|transcript distribution deduced from reporter protein
CVBODP|<t> E | gastrula <a> parasegment 6,8 <of> ectoderm <p>
}

REF
{
REFM|FBrf0055958
|Muller and Bienz
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000070	SYM 1 Ecol\lacZ<up>Ubx.pbxPPa</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 826
ID|FBtr0000070
SYM|Ecol\lacZ<up>Ubx.pbxPPa</up>RA
SYN|lacZ<up>Ubx.pbxPPa</up>RA
ASAL|<fbsym>FBal0042198==Ecol\lacZ<up>Ubx.pbxPPa</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000071
ASTP|<fbsym>FBtp0004627==P{lacZ<up>Ubx.pbxPPa</up>}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0055958
|Muller and Bienz
|1992
RNAT|mRNA
BODP|Faint staining is observed in narrow stripes in the dorsal epidermis of even
| parasegments 6-12. The pattern does not resemble the "ftz-like" stripe
| pattern of related Ubx.pbx constructs but rather a basal pattern observed
| in truncated <fbsym>FBgn0003944==Ubx</fbsym> promoter constructs.
ASM|transcript distribution deduced from reporter protein
CVBODP|<t> E <a> parasegment 6,8,10,12 <of> epidermis | dorsal <p>
}

REF
{
REFM|FBrf0055958
|Muller and Bienz
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000071	SYM 1 Antp<up>+</up>RA	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 5	DT 1 22 Aug 2000	RESZ 4649
ID|FBtr0000071
SYM|Antp<up>+</up>RA
SYN|P1
ASAL|<fbsym>FBal0066388==Antp<up>+</up></fbsym>
DT|22 Aug 2000
|10 Mar 1998
ID2|FBtr0000072
ASGN|<fbsym>FBgn0000095==Antp</fbsym>

REFDSR
{
RDID|FBrf0039287
|Garber et al.
|1983
RNAT|mRNA
CC|A 2.2kb cDNA was isolated from an early embryonic cDNA library. The cDNA
| hybridizes to four regions within a 100kb span of genomic DNA.
}

REFDSR
{
RDID|FBrf0039288
|Levine et al.
|1983
RNAT|mRNA
BODP|<fbsym>FBgn0000095==Antp</fbsym> transcripts are first detected in two dorso-lateral clusters of cells
| in the cellular blastoderm embryo that give rise to thoracic hypodermal
| derivatives: cuticle, glands, trachea, and imaginal discs. In germ band
| extended embryos, transcripts are predominantly observed in the thoracic
| sections of the CNS and in the overlying ectoderm. As the germ band
| retracts, expression fades in the ectoderm but persists in the CNS.
| Expression is strongest in the meso- and metathoracic segments but persists
| in the abdominal segments as well. With further developmental time,
| expression decreases in the metathoracic and abdominal segments but remains
| in the mesothoracic segment. Staining is more intense in the anterior part
| of the segment than in the posterior half. Expression persists in the
| ventral ganglion in larvae in the region corresponding to the mesothoracic
| segment. Signal is also seen in cells other than CNS cells. Some may
| correspond to hypodermally derived gland cells which will secrete the
| larval spiracle. In third instar larvae, expression is observed in specific
| regions of the prothoracic, mesothoracic and metathoracic discs.
ASM|radioisotope in situ
CVBODP|radioisotope in situ
|<t> E <a> ectoderm <p>
|<t> E <a> embryonic central nervous system | restricted <p>
|<t> E <a> embryonic mesothoracic segment <p>
|<t> L | third instar <a> dorsal mesothoracic disc | restricted <p>
|<t> L | third instar <a> dorsal metathoracic disc | restricted <p>
|<t> L | third instar <a> dorsal prothoracic disc | restricted <p>
}

REFDSR
{
RDID|FBrf0051576
|Bermingham et al.
|1990
RNAT|mRNA
BODP|<fbsym>FBgn0000095==Antp</fbsym> P1-containing transcripts are first detected early in nuclear cycle
| 14 in a ring surrounding the embryo extending from 40-55% egg length at the
| ventral surface. The ring is narrower at the dorsal surface. At
| gastrulation, expression extends to 17% egg length (PS12). In stage 8,
| expression is mainly observed in the ectoderm from posterior PS4 to
| anterior PS6 and more weakly from PS6 through PS12. In stages 11 and 12,
| P1-containing transcripts are found at high levels in epidermal cells from
| PS4, PS5, and anterior PS6 and in the mesoderm of PS5 and anterior PS6.
| They are detected in the developing ventral nerve cord at stage 11 in PS4
| and PS5. During stage 12, they decrease in the epidermis and increase in
| the CNS. After germ band retraction, expression is absent from the
| epidermis except for a few cells in the region of the primordium of the
| anterior spiracle. In the nervous system, P1-expressing transcripts are
| expressed at high levels in PS4, at lower levels in PS5, and at very low
| levels in PS6-PS12. In addition expression is observed in some specific
| muscle sets, in the visceral mesoderm, and in cells in or near the aorta.
ASM|in situ
CVBODP|in situ
|<t> E | early <a>  <p> 40-55% egg length
|<t> E | mid <a> parasegment 4..12 <p>
|<t> E | stage >=11 <a> ventral nerve cord <p>
|<t> E | stage 13 <a> embryonic/larval anterior spiracle | vicinity of <p>
|<t> E | late <a> embryonic central nervous system <p>
|<t> E | stage 17 <a> embryonic/larval aorta | vicinity of <p>
|<t> E | late <a> visceral mesoderm <of> anterior embryonic/larval midgut <p>
|<t> E | late <a> embryonic/larval muscle system <p>
}

REFDSR
{
RDID|FBrf0055836
|Roder et al.
|1992
RNAT|mRNA
AGT|<fbsym>FBal0032945==tsh<up>8</up></fbsym>
BODP|The spatial pattern of <fbsym>FBgn0000095==Antp</fbsym> transcripts appears as wild type in <fbsym>FBgn0003866==tsh</fbsym> mutants.
ASM|in situ
}

REFDSR
{
RDID|FBrf0056111
|Oh et al.
|1992
RNAT|mRNA
CC|P1-initiated transcripts contain a 1512-nucleotide 5' non coding region
| derived from sequences in non-protein coding exons A, B, D, and E. The
| first 55 nucleotides of exon D of the <fbsym>FBgn0000095==Antp</fbsym> gene were shown to mediate
| initiation of translation by providing an internal ribosome entry site
| (IRES) in cultured SL2 cells.
}

REF
{
REFM|FBrf0039287
|Garber et al.
|1983
REFM|FBrf0039288
|Levine et al.
|1983
REFM|FBrf0051576
|Bermingham et al.
|1990
REFM|FBrf0055836
|Roder et al.
|1992
REFM|FBrf0056111
|Oh et al.
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000072	SYM 1 Antp<up>+</up>RB	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 4	DT 1 22 Aug 2000	RESZ 3563
ID|FBtr0000072
SYM|Antp<up>+</up>RB
SYN|P2
ASAL|<fbsym>FBal0066388==Antp<up>+</up></fbsym>
DT|22 Aug 2000
|10 Mar 1998
ID2|FBtr0000073
ASGN|<fbsym>FBgn0000095==Antp</fbsym>

REFDSR
{
RDID|FBrf0039287
|Garber et al.
|1983
RNAT|mRNA
CC|A 2.9kb cDNA was isolated from a pupal cDNA library. The cDNA hybridizes to
| three regions within a 37kb span of genomic DNA. The first region falls
| within an intron of the larger <fbsym>FBgn0000095==Antp</fbsym> transcription unit and the second two
| regions are in common between the two transcription units.
}

REFDSR
{
RDID|FBrf0051576
|Bermingham et al.
|1990
RNAT|mRNA
BODP|<fbsym>FBgn0000095==Antp</fbsym> P2-containing transcripts are first detected in blastoderm stage
| embryos. They accumulate in a ring 3-4 cells wide centered around 56% egg
| length (at PS4). Two other bands of expression are observed in the
| primordia for PS6 (at the ventral surface) and at PS14 (encircling the
| embryo). At gastrulation, the PS4 expression remains strong, PS6 expression
| is only detected in cells that invaginate as part of the furrow and
| expressing cells in PS14 move dorsally with the pole cells. At stage 8,
| P2-containing transcripts are strongly expressed in the ectoderm of PS3 and
| PS4 and in the mesoderm of PS4 and PS6. They are expressed more weakly in
| the ectoderm and mesoderm of PS5 and in the ectoderm from PS6 to PS14, with
| stronger signals in even-numbered parasegments. At stage 11 in the
| epidermis, expression is limited to a subset of cells in PS3, PS4 and PS5
| ventrally and small clusters of cells in the center of PS 4-14 laterally.
| In the CNS, expression is in a subset of neural cells in each PS from PS3
| to the anus. During stage 12, expression decreases in the epidermis and
| increases in the nervous system. After stage 12, expression decreases to
| low levels in the epidermis but is present in cells below the epidermis
| that are probably sensory organ precursors. In the mature nervous system,
| expression is in a subset of neurons from PS3 to PS14. P2-expressing
| transcripts are also observed in the visceral mesoderm surrounding the
| anterior midgut, in most or all somatic muscles, and in the area of the
| aorta at stage 17.
ASM|in situ
CVBODP|in situ
|<t> E | blastoderm <a>  <p> 56% egg length
|<t> E | blastoderm <a> parasegment 6 | primordium <p>
|<t> E | blastoderm <a> parasegment 14 | primordium <p>
|<t> E | stage 8 <a> ectoderm <of> parasegment 3..14 <p>
|<t> E | stage 8 <a> mesoderm <of> parasegment 4..6 <p>
|<t> E | stage >=11 <a> embryonic central nervous system <p>
|<t> E | late <a> visceral mesoderm <of> anterior embryonic/larval midgut <p>
|<t> E | stage 17 <a> embryonic/larval aorta | vicinity of <p>
|<t> E | late <a> embryonic/larval somatic muscle <p>
}

REFDSR
{
RDID|FBrf0055836
|Roder et al.
|1992
RNAT|mRNA
AGT|<fbsym>FBal0032945==tsh<up>8</up></fbsym>
BODP|The spatial pattern of <fbsym>FBgn0000095==Antp</fbsym> transcripts appears as wild type in <fbsym>FBgn0003866==tsh</fbsym> mutants.
ASM|in situ
}

REFDSR
{
RDID|FBrf0056111
|Oh et al.
|1992
RNAT|mRNA
CC|P2-initiated transcripts contain a 1727-nucleotide 5' non coding region
| derived from exons C, D, and E. The first 55 nucleotides of exon D of the
| <fbsym>FBgn0000095==Antp</fbsym> gene were shown to mediate initiation of translation by providing an
| internal ribosome entry site (IRES) in cultured SL2 cells.
}

REF
{
REFM|FBrf0039287
|Garber et al.
|1983
REFM|FBrf0051576
|Bermingham et al.
|1990
REFM|FBrf0055836
|Roder et al.
|1992
REFM|FBrf0056111
|Oh et al.
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000099	SYM 1 snk<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 318
ID|FBtr0000099
SYM|snk<up>+</up>RA
ASAL|<fbsym>FBal0071112==snk<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000100
ASGN|<fbsym>FBgn0003450==snk</fbsym>

REFDSR
{
RDID|FBrf0045112
|DeLotto and Spierer
|1986
RNAT|mRNA
EXNSQ|1-4, 5a, 6
CC|pupal transcript
}

REF
{
REFM|FBrf0045112
|DeLotto and Spierer
|1986
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000105	SYM 1 elav<up>+</up>R	TRL 1 -	ASM 1 radioisotope in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 7 Apr 1998	RESZ 2672
ID|FBtr0000105
SYM|elav<up>+</up>R
ASAL|<fbsym>FBal0068902==elav<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000106
ASGN|<fbsym>FBgn0000570==elav</fbsym>

REFDSR
{
RDID|FBrf0046130
|Campos et al.
|1987
RNAT|mRNA
BODP|<fbsym>FBgn0000570==elav</fbsym> transcripts are present in the brain and ventral nervous system of
| 6-12 hr embryos. <fbsym>FBgn0000570==elav</fbsym> transcripts are also detected in pupal (low levels)
| and adult stages, and but not in the larva. Transcripts of 6.1 and 5.4 kb
| are detected in the adult.
ASM|radioisotope in situ
CVBODP|radioisotope in situ
|<t> E | 6-12 hr <a> embryonic nervous system <p>
}

REFDSR
{
RDID|FBrf0047824
|Robinow and White
|1988
RNAT|mRNA
BODP|<fbsym>FBgn0000570==elav</fbsym> transcript is first detected after stage 9 of embryogenesis. From
| stage 11 to stage 14, <fbsym>FBgn0000570==elav</fbsym> transcript is found in the central nervous
| system, and during stages 13-14, it is also detected in the dorsal
| ectoderm, in a segmentally repeated pattern. During larval development,
| <fbsym>FBgn0000570==elav</fbsym> is expressed in the medulla cortex of the larval brain, the ventral
| ganglion, as well as posterior to the morphogenetic furrow in the
| eye-antennal disc. During pupariation, <fbsym>FBgn0000570==elav</fbsym> transcript continues to be
| detected in the cortical regions of the central nervous system, and by the
| 96th hour of pupariation, is also expressed in an organ of the peripheral
| nervous system, the Johnston's organ. <fbsym>FBgn0000570==elav</fbsym> expression in this organ
| persists to adulthood. At 96 hours of pupariation, <fbsym>FBgn0000570==elav</fbsym> expression in the
| pupal head is seen in the cell bodies of the brain, optic lobes, and
| lamina, but is absent from the neuropils of these structures. Careful in
| situ analysis has shown that <fbsym>FBgn0000570==elav</fbsym> transcript is absent from neuroblasts
| during embryogenesis and larval development, although it is expressed, and
| persists, in postmitotic neurons, suggesting that <fbsym>FBgn0000570==elav</fbsym> function is
| required for the development and maintenance of neurons.
ASM|radioisotope in situ
CVBODP|radioisotope in situ
|<t> E | stage 11-14 <a> embryonic central nervous system | presumptive <p>
|<t> E | stage 13-14 <a> dorsal ectoderm <p> segmentally repeated
|<t> L | third instar <a> larval brain <p>
|<t> L | third instar <a> morphogenetic furrow | posterior to <p>
|<t> L | third instar <a> ventral ganglion <p>
|<t> P | 96 hr <a> thoracic ganglion  <p><t> A <a> Johnston's organ <p>
}

REF
{
REFM|FBrf0046130
|Campos et al.
|1987
REFM|FBrf0047824
|Robinow and White
|1988
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000110	SYM 1 Mhc<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 10	DT 1 6 Jan 2000	RESZ 9632
ID|FBtr0000110
SYM|Mhc<up>+</up>R
ASAL|<fbsym>FBal0068063==Mhc<up>+</up></fbsym>
DT|6 Jan 2000
|10 Mar 1998
ID2|FBtr0000111
ASGN|<fbsym>FBgn0002741==Mhc</fbsym>

REFDSR
{
RDID|FBrf0046579
|Wassenberg et al.
|1987
RNAT|mRNA
VPR|experimental
CC|Blotting, SI nuclease, primer extension, and DNA sequencing experiments were
| used to show that the larval and pupal <fbsym>FBgn0002741==Mhc</fbsym> transcripts all use the same
| transcription initiation site.
}

REFDSR
{
RDID|FBrf0049506
|Kazzaz and Rozek
|1989
RNAT|mRNA
BODP|Specific probes were designed to assay the tissue-specific use of the 18th
| exon and the alternative polyadenylation signals. It was found that
| embryonic muscles contain only transcripts lacking the 18th exon. In pupae,
| transcripts containing the 18th exonare found only in muscles of the leg,
| thorax, and head, while transcripts lacking the 18th exon are found in the
| body wall musculature of the abdomen. In both embryos and pupae, polyA site
| selection is not muscle-type specific.
ASM|in situ
}

REFDSR
{
RDID|FBrf0049799
|O'Donnell et al.
|1989
RNAT|mRNA
BODP|Probes common to all <fbsym>FBgn0002741==Mhc</fbsym> transcripts were used to show that <fbsym>FBgn0002741==Mhc</fbsym>
| transcripts are expressed in all muscles in late pupae. They are especially
| concentrated in indirect flight muscle, leg muscles and proboscis muscles.
| Little expression is seen in the abdomen.
ASM|radioisotope in situ
CVBODP|radioisotope in situ
|<t> P | late <a> indirect flight muscle <p>
|<t> P | late <a> proboscis muscle <p>
|<t> P | late <a> skeletal muscle of leg <p>
|<t> P | late <a> mesothoracic extracoxal depressor muscle 66 <p>
}

REFDSR
{
RDID|FBrf0050538
|George et al.
|1989
RNAT|mRNA
CC|The <fbsym>FBgn0002741==Mhc</fbsym> gene is composed of 19 exons. Five of these exons (3,7,9,11,15)
| are tandemly repeated as 2-5 divergent copies. In a given <fbsym>FBgn0002741==Mhc</fbsym> transcript
| one copy of each of these exons is present. In addition, exon 18 is found
| only in pupal and adult <fbsym>FBgn0002741==Mhc</fbsym> transcripts. There are at least 480 possible
| transcripts that can be encoded by these exons. RNA hybridization with
| exon-specific probes shows that at least 10 of the possible transcripts
| exist in the fly. These are regulated in a stage and muscle-specific
| manner. Evidence is presented on the use of each of the alternate exons in
| larval and pupal <fbsym>FBgn0002741==Mhc</fbsym> transcripts. Further, the use of exons 15a and 15b
| (which encode part of the hinge region of the protein) was studied in
| dissected tissues. In summary, Exons 7d, 11b, and 18 are pupal specific.
| Exons 3a, 7a, 7b, and 11c are not present in transcripts containing the
| thorax-specific exon 18, whereas exons 7d and 11b are predominantly
| expressed in pupal RNAs containing exon 18. Exon 15b is predominantly
| expressed in larvae while exon 15a is predominantly expressed in adults.
| Exons 15a and 15b are both expressed in thorax, but 15a is the exclusive
| form expressed in the IFM.
}

REFDSR
{
RDID|FBrf0050710
|Levin et al.
|1989
RNAT|mRNA
BODP|<fbsym>FBgn0002741==Mhc</fbsym> transcripts were detected in somatic and visceral muscles in late
| embryos and thoracic, abdominal, and leg muscles in late pupae. The pattern
| is similar to that of the adjacent gene <fbsym>FBgn0033189==Cyt-b5</fbsym>.
CVBODP|<t> E | stage 16 <a> somatic muscle <p>
|<t> E | stage 16 <a> visceral muscle <p>
|<t> P | late <a> skeletal muscle of thorax <p>
|<t> P | late <a> skeletal muscle of abdomen <p>
|<t> P | late <a> skeletal muscle of leg <p>
}

REFDSR
{
RDID|FBrf0051863
|Collier et al.
|1990
RNAT|mRNA
BODP|Antisense probes were used to determine the tissue specificity of alternate
| <fbsym>FBgn0002741==Mhc</fbsym> exon usage in wild type animals. Exon 15b is used in transcripts in
| all larval muscles while exon 15a shows no hybridization to larval muscles.
| In adults, exon15a but not 15b is found in indirect flight muscle and jump
| muscles. Both are used in various head and leg muscles. Indirect evidence
| from the distribution of functional muscles in Mhc[10] mutants (which lack
| exon 15a-containing transcripts) suggests that in wild type, exons 15a and
| 15b are about equally used in intracoxal levator muscles, that 15a is the
| predominant form in intracoxal depressor muscles, and that 15b is the form
| used in dorsal body wall muscles. Antisense RNA probes were also used to
| study the distribution of exon 15a and 15b-containing <fbsym>FBgn0002741==Mhc</fbsym> transcripts in
| Mhc[10] mutants at different developmental stages. The pattern of larval
| transcription is unchanged in the mutant as determined by hybridization to
| exon 15b. In pupae, both larval size classes of RNA (6.1kb and 6.6kb)
| accumulate normally. The transcripts (6.6kb and 7.1kb) that normally appear
| first in pupae and are detected with exon 15a are absent.
ASM|miscellaneous
CVBODP|miscellaneous
|<t> L <a> larval muscle system <p>
|<t> A <a> indirect flight muscle <p>
|<t> A <a> mesothoracic extracoxal depressor muscle 66 <p>
|<t> A <a> intracoxal depressor muscle <p>
|<t> A <a> intracoxal levator muscle <p>
|<t> A <a> skeletal muscle ofhead <p>
|<t> A <a> skeletal muscle of leg <p>
|<t> A <a> skeletal muscle of abdomen <p>
}

REFDSR
{
RDID|FBrf0053362
|Corbin et al.
|1991
RNAT|mRNA
AGT|<fbsym>FBal0002638==Dl<up>X</up></fbsym>
|<fbsym>FBal0012750==N<up>264-47</up></fbsym>
BODP|In the neurogenic mutants, <fbsym>FBgn0002741==Mhc</fbsym> expression is induced in the mesoderm but
| the cells are arranged in irregular clusters.
ASM|in situ
CVBODP|<t> E <a> somatic mesoderm <p>
|<t> E <a> larval somatic muscle <p>
}

REFDSR
{
RDID|FBrf0053881
|Kronert et al.
|1991
RNAT|mRNA
BODP|Use of <fbsym>FBgn0002741==Mhc</fbsym> exons 9a, 9b, and 9c in wild type was studied by northern blots
| and in situ hybridization. Exon 9a is found only at the pupal stage in the
| 6.6kb and 7.1kb transcripts (which also include exon 18). Exon 9b is used
| in all size classes of RNA in both larvae and pupae. Exon 9c is used at
| both stages but only in transcripts that lack exon 18 (6.1kb and 6.6kb). In
| pupae, exons 9a and 9b are used in roughly equivalent amounts and are each
| ~2.5 times more abundant than transcripts containing exon 9c. In larvae,
| exon 9b-containing transcripts are 16-fold more abundant than those
| containing exon 9c. In adult sections, the exon 9a probe hybridizes
| strongly to thoracic musculature but not to leg or cephalic muscles. Within
| the thorax, it accumulates in the indirect flight muscles and in both the
| small and large cells of the jump muscles, but not the pleurosternal
| muscles. Exon 9b hybridizes to thoracic muscles, and to leg and proboscis
| muscles. In the thorax, it is found in the large cells of the jump muscles
| and in the pleurosternal muscles, but not in the IFM. Exon 9c-containing
| transcripts were not detected but are thought to accumulate in visceral
| musculature and body wall muscles. <fbsym>FBgn0002741==Mhc</fbsym> transcription in the <fbsym>FBal0012252==Mhc[11]</fbsym>
| mutant was also studied.
ASM|northern blot
|in situ
CVBODP|in situ
|<t> A <a> indirect flight muscle <p>
|<t> A <a> mesothoracic pleurosternal muscle <p>
|<t> A <a>  mesothoracic extracoxal depressor muscle 66 <p>
|<t> A <a> proboscis muscle <p>
|<t> A <a> skeletal muscle of leg <p>
}

REFDSR
{
RDID|FBrf0054371
|Hastings and Emerson
|1991
RNAT|mRNA
BODP|Muscle-specific expression of <fbsym>FBgn0002741==Mhc</fbsym> exons was studied by in situ
| hybridization. It was found that for each exon set examined, only one
| isoform was detectable in each of the muscles studied (IFM, TDT, DFM, and
| esophagus). Exon 3b was present in all of the muscles. For exon 7, 7d is
| present in IFM, 7a and 7d in tubular muscle and 7a in esophageal muscle
| (visceral muscle). For exon 11, only exon 11e is expressed in IFM, 11b is
| expressed in the TDT and DFM #51, and 11c in DFM #52 and esophageal muscle.
| For exon 15, 15a is expressed in IFM, TDT, DFM #51 and 15b in DFMs #49, 52,
| and 53 and esophageal muscle. Exon 9 isoform expression was not determined.
| It was shown that different <fbsym>FBgn0002741==Mhc</fbsym> isoforms are expressed in the three major
| muscle types in the adult thorax.
ASM|in situ
}

REFDSR
{
RDID|FBrf0091196
|Wells et al.
|1996
RNAT|mRNA
CC|<fbsym>FBgn0002741==Mhc</fbsym> transcripts are generated by alternative splicing. Of the 19 exons, 5
| are alternatively spliced sets (3,7,9,11,15) and one is either excluded or
| included (18). It does not appear that transcripts containing all of the
| possible combinations of exons are actually produced in the fly. cDNAs were
| isolated and characterized as to which of the alternate exons they contain.
| None contain exon 18. The combinations (only alternate exon forms are
| specified) that were isolated were 1)3a,7a,9b,11d,15b 2)3a,7a,9c,11e,15b
| 3)3b,7a,9b,11d,15b and 4)3b,7a,9b,11b,15b. Form 1 (which is normally
| expressed in embryos) was transformed into flies behind a <fbsym>FBgn0002741==Mhc</fbsym> promoter
| and expressed in all muscles. It was used to study isoform specificity of
| <fbsym>FBgn0002741==Mhc</fbsym> function.
}

REF
{
REFM|FBrf0046579
|Wassenberg et al.
|1987
REFM|FBrf0049506
|Kazzaz and Rozek
|1989
REFM|FBrf0049799
|O'Donnell et al.
|1989
REFM|FBrf0050538
|George et al.
|1989
REFM|FBrf0050710
|Levin et al.
|1989
REFM|FBrf0051863
|Collier et al.
|1990
REFM|FBrf0053362
|Corbin et al.
|1991
REFM|FBrf0053881
|Kronert et al.
|1991
REFM|FBrf0054371
|Hastings and Emerson
|1991
REFM|FBrf0091196
|Wells et al.
|1996
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000111	SYM 1 Mhc<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 558
ID|FBtr0000111
SYM|Mhc<up>+</up>RA
ASAL|<fbsym>FBal0068063==Mhc<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000112
ASGN|<fbsym>FBgn0002741==Mhc</fbsym>
ASPP|<fbsym>FBpp0001628==Mhc<up>+</up>PB</fbsym>

REFDSR
{
RDID|FBrf0046579
|Wassenberg et al.
|1987
RNAT|mRNA
EXNSQ|1,2,3a,4,5
CC|Two exon 3 sequences were found that would encode different <fbsym>FBgn0002741==Mhc</fbsym> proteins
| (17 of 48 amino acids encoded by the exon differ) but no direct evidence
| was presented that both are used.
}

REF
{
REFM|FBrf0046579
|Wassenberg et al.
|1987
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000112	SYM 1 Mhc<up>+</up>RB	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 558
ID|FBtr0000112
SYM|Mhc<up>+</up>RB
ASAL|<fbsym>FBal0068063==Mhc<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000113
ASGN|<fbsym>FBgn0002741==Mhc</fbsym>
ASPP|<fbsym>FBpp0001629==Mhc<up>+</up>PC</fbsym>

REFDSR
{
RDID|FBrf0046579
|Wassenberg et al.
|1987
RNAT|mRNA
EXNSQ|1,2,3b,4,5
CC|Two exon 3 sequences were found that would encode different <fbsym>FBgn0002741==Mhc</fbsym> proteins
| (17 of 48 amino acids encoded by the exon differ) but no direct evidence
| was presented that both are used.
}

REF
{
REFM|FBrf0046579
|Wassenberg et al.
|1987
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000128	SYM 1 H<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 1728
ID|FBtr0000128
SYM|H<up>+</up>R
ASAL|<fbsym>FBal0067871==H<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000129
ASGN|<fbsym>FBgn0001169==H</fbsym>
SK|FBst1001750
|(w);  <fbsym>FBal0067871==H[+]</fbsym> Pr[1] Bsb[1]/TM2 (6?)
|Total=1

REFDSR
{
RDID|FBrf0056117
|Bang and Posakony
|1992
RNAT|mRNA
BODP|<fbsym>FBgn0001169==H</fbsym> transcripts are detected in ovaries in nurse cells. Maternal transcripts
| are present in syncytial embryos until cellular blastoderm. Zygotic
| transcripts are broadly distributed throughout the embryo during germband
| extension and retraction. They initially accumulate at higher levels in the
| mesodermal layer and are consistently seen at lower levels in the head
| region particulary in the procephalic lobe and the clypeolabrum. <fbsym>FBgn0001169==H</fbsym>
| transcripts are observed in the developing CNS at the time of action of the
| zygotic neurogenic genes. A widespread, uniform distribution of transcripts
| is seen in late third instar larval imaginal discs. In early pupae, a
| uniform distribution is seen in notal epithelium with the exception of two
| cells that show a higher level of transcript accumulation. Later, elevated
| levels of <fbsym>FBgn0001169==H</fbsym> expression are seen in cells that have been identified as the
| tormogen and trichogen cells.
ASM|in situ
CVBODP|<t> O,A <a> nurse cell <p>
|<t> E <a> mesoderm <p>
|<t> E <a> head <p>
|<t> E <a> labral segment <p>
|<t> E <a> procephalic segment <p>
|<t> E <a> central nervous system <p>
|<t> L | third instar stage 2 <a> imaginal disc <p>
|<t> P | early <a> epithelial cell <of> dorsal mesothoracic disc <p>
|<t> P | >16 hr <a> tormogen cell <p>
}

REF
{
REFM|FBrf0056117
|Bang and Posakony
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000149	SYM 1 Pkn<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 30 Jun 1999	RESZ 302
ID|FBtr0000149
SYM|Pkn<up>+</up>RA
SYN|Pk45C<up>+</up>RA
ASAL|<fbsym>FBal0079604==Pkn<up>+</up></fbsym>
DT|30 Jun 1999
|10 Mar 1998
ID2|FBtr0000150
ASGN|<fbsym>FBgn0020621==Pkn</fbsym>

REFDSR
{
RDID|FBrf0048100
|Kalderon and Rubin
|1988
RNAT|mRNA
}

REF
{
REFM|FBrf0048100
|Kalderon and Rubin
|1988
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000152	SYM 1 for<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 279
ID|FBtr0000152
SYM|for<up>+</up>RA
ASAL|<fbsym>FBal0068959==for<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000153
ASGN|<fbsym>FBgn0000721==for</fbsym>

REFDSR
{
RDID|FBrf0048100
|Kalderon and Rubin
|1988
RNAT|mRNA
}

REF
{
REFM|FBrf0048100
|Kalderon and Rubin
|1988
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000159	SYM 1 otu<up>+</up>R	TRL 1 -	ASM 1 radioisotope in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 16 Sep 1998	RESZ 940
ID|FBtr0000159
SYM|otu<up>+</up>R
SYN|K
ASAL|<fbsym>FBal0070856==otu<up>+</up></fbsym>
DT|16 Sep 1998
|10 Mar 1998
ID2|FBtr0000160
ASGN|<fbsym>FBgn0003023==otu</fbsym>

REFDSR
{
RDID|FBrf0048651
|Mulligan et al.
|1988
RNAT|mRNA
BODP|Three to four <fbsym>FBgn0003023==otu</fbsym> transcripts in the 3.5kb to 4.5kb size range are
| detected in testis RNA.
ASM|dissected tissue
CVBODP|dissected tissue
|<t> A,S <a> testis <p>
}

REFDSR
{
RDID|FBrf0063780
|Parks and Spradling
|1987
RNAT|mRNA
BODP|<fbsym>FBgn0003023==otu</fbsym> transcript is detected in nurse cells from stage S6 to stage S10B.
| <fbsym>FBgn0003023==otu</fbsym> transcript begins to be detected in the oocyte from stage S10A
| onwards, and is distributed uniformly in the oocyte after the nurse cell
| breakdown at stage S10B.
ASM|radioisotope in situ
CVBODP|radioisotope in situ
}

REF
{
REFM|FBrf0048651
|Mulligan et al.
|1988
REFM|FBrf0063780
|Parks and Spradling
|1987
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000160	SYM 1 ct<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 7 Apr 1998	RESZ 1504
ID|FBtr0000160
SYM|ct<up>+</up>R
ASAL|<fbsym>FBal0068792==ct<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000161
ASGN|<fbsym>FBgn0004198==ct</fbsym>

REFDSR
{
RDID|FBrf0048770
|Blochlinger et al.
|1988
RNAT|mRNA
CC|Fragments of the 8.2 kb sequence hybridize to at least two transcripts of
| 8.5 and 9.5 kb on Northern blots of early and late embryos. A 2175 amino
| acid protein is predicted from the 8.2 kb sequence.
}

REFDSR
{
RDID|FBrf0051828
|Blochlinger et al.
|1990
RNAT|mRNA
BODP|The pattern of <fbsym>FBgn0004198==ct</fbsym> transcript expression during embryogenesis matches that
| of <fbsym>FBgn0004198==ct</fbsym> protein expression. The precursors of the external sensory organs,
| and later the trichogen, tormogen, thecogen and neuron of most of the
| externalsensory organs express <fbsym>FBgn0004198==ct</fbsym>. The region surrounding the anterior
| and posterior spiracle precursors, the Malpighian tubule, and a subset of
| the CNS express the <fbsym>FBgn0004198==ct</fbsym> transcript starting at 5-7 hours of embryogenesis.
ASM|in situ
CVBODP|in situ
|<t> E | >5-6 hr <a> external sensory organ <p>
|<t> E | >5-6 hr <a> embryonic/larval posterior spiracle | surrounding <p>
|<t> E | >5-6 hr <a> embryonic/larval anterior spiracle | surrounding <p>
|<t> E | >5-6 hr <a> Malpighian tubule <p>
|<t> E | >6-7 hr <a> embryonic central nervous system | presumptive | restricted <p>
}

REF
{
REFM|FBrf0048770
|Blochlinger et al.
|1988
REFM|FBrf0051828
|Blochlinger et al.
|1990
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000169	SYM 1 Ecol\lacZ<up>Sry-&agr;.C&agr;N'&bgr;G</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 1447
ID|FBtr0000169
SYM|Ecol\lacZ<up>Sry-&agr;.C&agr;N'&bgr;G</up>RA
SYN|lacZ<up>Sry-alpha.CalphaN'betaG</up>RA
ASAL|<fbsym>FBal0047532==Ecol\lacZ<up>Sry-&agr;.C&agr;N'&bgr;G</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000170
ASTP|<fbsym>FBtp0005472==P{C&agr;N'&bgr;G}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0049479
|Schweisguth et al.
|1989
RNAT|mRNA
BODP|In flies transformed with <fbsym>FBgn0003510==Sry-alpha</fbsym>-<fbsym>FBgn0014447==Ecol\lacZ</fbsym> constructs,
| <fbsym>FBgn0014447==Ecol\lacZ</fbsym> expression was detected in the cellular blastoderm embryo in
| all but the pole cells. Expression was weaker in the
| <fbsym>lacZ[Sry-alpha.CalphaNbetaG]</fbsym> and the <fbsym>lacZ[Sry-alpha.CalphaN'betaG]</fbsym>
| lines, which lack Sry-alpha sequences upstream from -311. The same two
| lines also showed neural expression during embryogenesis, which was not
| seen with the other lines, or in wild type <fbsym>FBgn0003510==Sry-alpha</fbsym>. The -118 to +130
| region was sufficient for cellular blastoderm expression, which was
| enhanced with the -311 to -118 region. The latter domain might contain
| negative regulatory elements, the removal of which would allow nervous
| system expression.
CVBODP|transcript distribution deduced from reporter protein
|<t> E | cellular blastoderm <a>  <p>
|<t> E | mid-late <a> embryonic nervous system <p>
}

REF
{
REFM|FBrf0049479
|Schweisguth et al.
|1989
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000170	SYM 1 Ecol\lacZ<up>Sry-&agr;.C&agr;N&bgr;G</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 1473
ID|FBtr0000170
SYM|Ecol\lacZ<up>Sry-&agr;.C&agr;N&bgr;G</up>RA
SYN|lacZ<up>Sry-alpha.CalphaNbetaG</up>RA
ASAL|<fbsym>FBal0047531==Ecol\lacZ<up>Sry-&agr;.C&agr;N&bgr;G</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000171
ASTP|<fbsym>FBtp0005471==P{C&agr;N&bgr;G}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0049479
|Schweisguth et al.
|1989
RNAT|mRNA
BODP|In flies transformed with <fbsym>FBgn0003510==Sry-alpha</fbsym>-<fbsym>FBgn0014447==Ecol\lacZ</fbsym> constructs,
| <fbsym>FBgn0014447==Ecol\lacZ</fbsym> expression was detected in the cellular blastoderm embryo in
| all but the pole cells. Expression was weaker in the
| <fbsym>lacZ[Sry-alpha.CalphaNbetaG]</fbsym> and the <fbsym>lacZ[Sry-alpha.CalphaN'betaG]</fbsym>
| lines, which lack Sry-alpha sequences upstream from -311. The same two
| lines also showed neural expression during embryogenesis, which was not
| seen with the other lines, or in wild type Sry-alpha. The -118 to +130
| region was sufficient for cellular blastoderm expression, which was
| enhanced with the -311 to -118 region. The latter domain might contain
| negative regulatory elements, the removal of which would allow nervous
| system expression.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E | cellular blastoderm <a>  <p>
|<t> E | mid-late <a> embryonic nervous system <p>
}

REF
{
REFM|FBrf0049479
|Schweisguth et al.
|1989
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000272	SYM 1 trx<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 3	DT 1 30 May 2001	RESZ 1590
ID|FBtr0000272
SYM|trx<up>+</up>R
ASAL|<fbsym>FBal0071404==trx<up>+</up></fbsym>
DT|30 May 2001
|10 Mar 1998
ID2|FBtr0000273
ASGN|<fbsym>FBgn0003862==trx</fbsym>

REFDSR
{
RDID|FBrf0050834
|Mozer and Dawid
|1989
RNAT|mRNA
BODP|<fbsym>FBgn0003862==trx</fbsym> transcripts are distributed ubiquitously through the early embryo. In
| later embryos, prominent labelling is observed in the ventral nerve cord.
ASM|in situ
CVBODP|in situ
|<t> E | early <a>  <p> ubiquitous
|<t> E <a> ventral nerve cord <p>
}

REFDSR
{
RDID|FBrf0076508
|Kuzin et al.
|1994
RNAT|mRNA
BODP|<fbsym>FBgn0003862==trx</fbsym> transcripts are observed in the eye-antennal disc and in the posterior
| regions of the wing, haltere, and metathoracic leg discs in a pattern
| similar to the distribution of <fbsym>FBgn0003862==trx</fbsym> protein.
ASM|in situ
CVBODP|in situ
|<t> E <a> embryonic central nervous system <p>
|<t> L | third instar <a> dorsal mesothoracic disc | posterior <p>
|<t> L | third instar <a> dorsal metathoracic disc | posterior <p>
|<t> L | third instar <a> eye-antennal disc <p>
|<t> L | third instar<a> ventral mesothoracic disc | posterior <p>
|<t> L | third instar <a> imaginal disc <p>
}

REFDSR
{
RDID|FBrf0084401
|Stassen et al.
|1995
RNAT|mRNA
CC|<fbsym>FBgn0003862==trx</fbsym> transcripts appear to use one major transcription start site and two
| major polyadenylation sites. Alternative splicing and polyadenylation is
| used to generate multiple transcripts.
}

REF
{
REFM|FBrf0050834
|Mozer and Dawid
|1989
REFM|FBrf0076508
|Kuzin et al.
|1994
REFM|FBrf0084401
|Stassen et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000300	SYM 1 Nrt<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 1051
ID|FBtr0000300
SYM|Nrt<up>+</up>R
ASAL|<fbsym>FBal0068126==Nrt<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000301
ASGN|<fbsym>FBgn0004108==Nrt</fbsym>

REFDSR
{
RDID|FBrf0051554
|Hortsch et al.
|1990
RNAT|mRNA
BODP|<fbsym>FBgn0004108==Nrt</fbsym> transcripts are first detected at the cellular blastoderm stage in a
| domain extending from 10-90% egg length ventrally and from 45-85% egg
| length dorsally. Later in development, they are restricted largely to the
| CNS and to a subset ofthe PNS, including sensory neurons in the head and
| posterior regions. They are also observed in the fat body.
ASM|in situ
CVBODP|in situ
|<t> E | cellular blastoderm <a>  <p> 10-90% egg length <and> ventral
|<t> E | cellular blastoderm <a>  <p> 45-85% egg length <and> dorsal
|<t> E | stage >=9 <a> embryonic central nervous system | presumptive <p>
|<t> E | stage >=9 <a> embryonic nervous system <p>
|<t> E <a> embryonic peripheral nervous system | restricted <p>
|<t> E <a> fat body primordium <p>
}

REF
{
REFM|FBrf0051554
|Hortsch et al.
|1990
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000314	SYM 1 sgg<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 495
ID|FBtr0000314
SYM|sgg<up>+</up>R
ASAL|<fbsym>FBal0071039==sgg<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000315
ASGN|<fbsym>FBgn0003371==sgg</fbsym>

REFDSR
{
RDID|FBrf0051642
|Bourouis et al.
|1990
RNAT|mRNA
BODP|Hybridization with a probe common to all <fbsym>FBgn0003371==sgg</fbsym> transcripts reveals that they
| are uniformly distributed in the embryo and are found in all germ layers
| throughout embryogenesis.
ASM|in situ
}

REF
{
REFM|FBrf0051642
|Bourouis et al.
|1990
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000317	SYM 1 mam<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 3	DT 1 7 Apr 1998	RESZ 4972
ID|FBtr0000317
SYM|mam<up>+</up>R
ASAL|<fbsym>FBal0070572==mam<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000318
ASGN|<fbsym>FBgn0002643==mam</fbsym>

REFDSR
{
RDID|FBrf0051833
|Smoller et al.
|1990
RNAT|mRNA
BODP|During embryonic germ-band elongation, the <fbsym>FBgn0002643==mam</fbsym> transcript is expressed
| ubiquitously. As embryogenesis proceeds, <fbsym>FBgn0002643==mam</fbsym> transcript gets more
| restricted to neural tissue, and by the 16th hour of embryogenesis, <fbsym>FBgn0002643==mam</fbsym>
| transcript is found predominantly in the ventral nerve cord and the brain.
ASM|radioisotope in situ
CVBODP|radioisotope in situ
|<t> E | 5 hr <a>  <p> ubiquitous
|<t> E | 16 hr <a> ventral nerve cord <p>
|<t> E | 16 hr <a> larval brain <p>
}

REFDSR
{
RDID|FBrf0053735
|Bettler et al.
|1991
RNAT|mRNA
BODP|A study of the expression pattern of the neurogenic gene <fbsym>FBgn0002643==mam</fbsym> up to the
| completion of gastrulation reveals early, ubiquitous expression, followed
| by preferential accumulation in ventral regions, including the mesoderm,
| endoderm, mesectoderm,and neurectoderm. In the cellular blastoderm stage,
| <fbsym>FBgn0002643==mam</fbsym> expression is ubiquitous. During early gastrulation, the expression
| of <fbsym>FBgn0002643==mam</fbsym> intensifies in the prospective mesoderm and endoderm. Later in
| gastrulation, <fbsym>FBgn0002643==mam</fbsym> expression is seen in the ventral furrow, the mesoderm,
| and a section of the ventral ectoderm which includes the mesectoderm and
| part of the neurectoderm. Expression is also seen in the anterior and
| posterior midgut primordia. At the completion of gastrulation, <fbsym>FBgn0002643==mam</fbsym>
| transcript continues to be detected in all of these tissues, as well as in
| the cephalic furrow.
ASM|in situ
CVBODP|in situ
|<t> E | cellular blastoderm <a>  <p> ubiquitous
|<t> E | gastrula <a> mesoderm | presumptive <p>
|<t> E | gastrula | early <a> endoderm | presumptive <p>
|<t> E | gastrula | early <a> ventral furrow <p>
|<t> E | gastrula <a> anterior midgut primordium<p>
|<t> E | gastrula | late <a> posterior midgut primordium <p>
|<t> E | gastrula | late <a> ectoderm | ventral <p>
|<t> E | gastrula | late <a> mesectoderm <p>
|<t> E | gastrula | late <a> neurectoderm | restricted <p>
|<t> E | gastrula | late <a> cephalic furrow <p>
}

REFDSR
{
RDID|FBrf0087692
|Schmid et al.
|1996
RNAT|mRNA
BODP|The <fbsym>FBgn0002643==mam</fbsym> transcript is detected in both neural and non-neural tissues. In
| the cellular blastoderm stage of embryogenesis, the <fbsym>FBgn0002643==mam</fbsym> transcript is
| detected at high levels in the cytoplasm of somatic cells, but is not
| expressed athigh levels in the pole cells. During gastrulation, <fbsym>FBgn0002643==mam</fbsym>
| transcript is found in the ventral and cephalic furrows, and in the gut
| rudiments. At germ band elongation, the expression of <fbsym>FBgn0002643==mam</fbsym> is highest in
| the cells of the germ band, including the mesoderm, the neural layer, and
| the gut primordia. The levels of <fbsym>FBgn0002643==mam</fbsym> in the midgut decline at germ band
| retraction, but remain high in the foregut and hindgut primordia, as well
| as in the brain and in the ventral nerve cord, in a segmentally repeated
| pattern. At stage 13 of embryogenesis, <fbsym>FBgn0002643==mam</fbsym> is detected in midline CNS
| cells, as well as in lateral clusters of CNS cells. In larvae, <fbsym>FBgn0002643==mam</fbsym>
| transcript is present uniformly in leg and wing imaginal discs, and at high
| levels anterior to the morphogenetic furrow in eye-antennal discs. Although
| present at moderate levels early in oogenesis, <fbsym>FBgn0002643==mam</fbsym> transcript is not
| detectable at stages 7 and 8. The transcript reapppears in stage 9 of
| oogenesis, and is detected at high levels in follicle cells, nurse cells,
| and oocytes at stage 10 of oogenesis.
ASM|in situ
CVBODP|in situ
|<t> E | gastrula <a> ventral furrow <p>
|<t> E | gastrula <a> cephalic furrow <p>
|<t> E | gastrulation <a> embryonic/larval digestive system | rudiment <p>
|<t> E | extended germ band stage <a> germ band <p>
|<t> E | contracted germ band stage <a> hindgut primordium <p>
|<t> E | contracted germ band stage <a> ventral nerve cord | segmentally repeated pattern <p>
|<t> E | stage 13 <a> ventral midline <p>
|<t> E | stage 13-17 <a> ventral nerve cord <p>
|<t> E | stage 13 <a> embryonic/larval foregut <p>
|<t> L <a> ventral thoracic disc <p>
|<t> L <a> dorsal mesothoracic disc <p>
|<t> L <a> eye-antennal disc <p>
|<t> L <a> morphogenetic furrow | anterior to <p>
|<t> O,A | early <a> nurse cell <p>
|<t> O,A | stage S10 <a> follicle cell <p>
|<t> O,A | stage S10 <a> nurse cell <p>
|<t> O,A | stage S10 <a> oocyte <p>
|<t> P | early <a> central nervous system | restricted <p>
}

REF
{
REFM|FBrf0051833
|Smoller et al.
|1990
REFM|FBrf0053735
|Bettler et al.
|1991
REFM|FBrf0087692
|Schmid et al.
|1996
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000355	SYM 1 Shab<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 324
ID|FBtr0000355
SYM|Shab<up>+</up>RA
ASAL|<fbsym>FBal0068313==Shab<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000356
ASGN|<fbsym>FBgn0003383==Shab</fbsym>
ASPP|<fbsym>FBpp0001247==Shab<up>+</up>P924</fbsym>

REFDSR
{
RDID|FBrf0052716
|Butler et al.
|1990
RNAT|mRNA
}

REF
{
REFM|FBrf0052716
|Butler et al.
|1990
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000357	SYM 1 Shal<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 2	DT 1 7 Apr 1998	RESZ 416
ID|FBtr0000357
SYM|Shal<up>+</up>RA
ASAL|<fbsym>FBal0074236==Shal<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000358
ASGN|<fbsym>FBgn0005564==Shal</fbsym>
ASPP|<fbsym>FBpp0001251==Shal<up>+</up>P490</fbsym>

REFDSR
{
RDID|FBrf0052716
|Butler et al.
|1990
RNAT|mRNA
}

REFDSR
{
RDID|FBrf0052940
|Wei et al.
|1990
RNAT|mRNA
}

REF
{
REFM|FBrf0052716
|Butler et al.
|1990
REFM|FBrf0052940
|Wei et al.
|1990
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000361	SYM 1 zip<up>+</up>RA	TRL 1 -	ASM 1 RNase protection, primer extension, SI etc.	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 2	DT 1 6 Jan 2000	RESZ 1452
ID|FBtr0000361
SYM|zip<up>+</up>RA
ASAL|<fbsym>FBal0071514==zip<up>+</up></fbsym>
DT|6 Jan 2000
|10 Mar 1998
ID2|FBtr0000362
ASGN|<fbsym>FBgn0005634==zip</fbsym>
ASPP|<fbsym>FBpp0001532==zip<up>+</up>P1972</fbsym>
|<fbsym>FBpp0002889==zip<up>+</up>P500</fbsym>

REFDSR
{
RDID|FBrf0047921
|Zhao et al.
|1988
RNAT|mRNA
BODP|<fbsym>FBgn0005634==zip</fbsym> transcripts are first detected after 6hr embryos. In situ
| hybridization reveals CNS-specific expression in late extended germ band
| stage embryos. Transcript levels increase during germ band retraction.
| Transcripts accumulate in the developing CNS until hatching.
CVBODP|in situ
|<t> E <a> embryonic central nervous system <p>
}

REFDSR
{
RDID|FBrf0052857
|Ketchum et al.
|1990
RNAT|mRNA
VPR|experimental
BODP|The "long" <fbsym>FBgn0005634==zip</fbsym> transcript which uses the second splice donor in exon 1 is
| 3.5X less abundant than the "short" form in all stages tested.
ASM|RNase protection, primer extension, SI etc.
|pcr
CVBODP|RNase protection, primer extension, SI etc.
|<t> E,A <a>  <p>
CC|Different classes of <fbsym>FBgn0005634==zip</fbsym> transcripts are generated by the use of two
| splice donor sites in the first exon. The second splice donor is 64 bases
| downstream of the first. The cDNA sequence in AC# M35012 contains the
| entire first exon (spliced at the downstream donor site).
}

REF
{
REFM|FBrf0047921
|Zhao et al.
|1988
REFM|FBrf0052857
|Ketchum et al.
|1990
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000362	SYM 1 zip<up>+</up>RB	TRL 1 -	ASM 1 RNase protection, primer extension, SI etc.	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 836
ID|FBtr0000362
SYM|zip<up>+</up>RB
ASAL|<fbsym>FBal0071514==zip<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000363
ASGN|<fbsym>FBgn0005634==zip</fbsym>
ASPP|<fbsym>FBpp0001532==zip<up>+</up>P1972</fbsym>

REFDSR
{
RDID|FBrf0052857
|Ketchum et al.
|1990
RNAT|mRNA
VPR|experimental
BODP|The "short" <fbsym>FBgn0005634==zip</fbsym> transcript which uses the first splice donor in exon 1 is
| 3.5X more abundant than the "long" form in all stages tested.
ASM|RNase protection, primer extension, SI etc.
|pcr
CVBODP|RNase protection, primer extension, SI etc.
|<t> E,A <a>  <p>
CC|Different classes of <fbsym>FBgn0005634==zip</fbsym> transcripts are generated by the use of two
| splice donor sites in the first exon. The second splice donor is 64 bases
| downstream of the first.
}

REF
{
REFM|FBrf0052857
|Ketchum et al.
|1990
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000366	SYM 1 Shal<up>+</up>RB	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 318
ID|FBtr0000366
SYM|Shal<up>+</up>RB
ASAL|<fbsym>FBal0074236==Shal<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000367
ASGN|<fbsym>FBgn0005564==Shal</fbsym>
ASPP|<fbsym>FBpp0001653==Shal<up>+</up>P605</fbsym>

REFDSR
{
RDID|FBrf0052940
|Wei et al.
|1990
RNAT|mRNA
}

REF
{
REFM|FBrf0052940
|Wei et al.
|1990
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000406	SYM 1 Ecol\lacZ<up>en-AuI</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 28 Jul 1999	RESZ 1212
ID|FBtr0000406
SYM|Ecol\lacZ<up>en-AuI</up>RA
SYN|lacZ<up>Au1</up>RA
|lacZ<up>en-AuI</up>RA
ASAL|<fbsym>FBal0047662==Ecol\lacZ<up>en-AuI</up></fbsym>
DT|28 Jul 1999
|10 Mar 1998
ID2|FBtr0003779
|FBtr0000407
ASTI|<fbsym>FBti0003682==P{lwB}en<up>AuI</up></fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
SK|FBst0006942
|w[*]; P{w[+mW.hs]=lwB}en[AuI]/CyO
|Total=1

REFDSR
{
RDID|FBrf0053395
|Klambt et al.
|1991
RNAT|mRNA
BODP|Enhancer trap expression is observed only in the posterior pair of midline
| glia (MGP).
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> midline glial cell <p>
}

REFDSR
{
RDID|FBrf0084424
|Sun et al.
|1995
RNAT|mRNA
BODP|In embryo, "patterned" expression.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a>  <p>
|<t> L | third instar <a> antennal disc | restricted <p>
|<t> L | third instar <a> dorsal mesothoracic disc | restricted <p>
|<t> L | third instar <a> ventral thoracic disc | restricted <p>
ASCRGN|<fbsym>FBgn0000577==en</fbsym>
}

REF
{
REFM|FBrf0053395
|Klambt et al.
|1991
REFM|FBrf0084424
|Sun et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000418	SYM 1 Ecol\lacZ<up>eve.ET-L</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 599
ID|FBtr0000418
SYM|Ecol\lacZ<up>eve.ET-L</up>RA
SYN|lacZ<up>eve.ET-L</up>RA
ASAL|<fbsym>FBal0044003==Ecol\lacZ<up>eve.ET-L</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000419
ASTP|<fbsym>FBtp0000853==P{ET-L}</fbsym>
|<fbsym>FBmc0000904==pP{ET-L}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0053745
|Perrimon et al.
|1991
RNAT|mRNA
BODP|Subcellular localization: cytoplamic.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t>  <a> cytoplasm <p>
}

REF
{
REFM|FBrf0053745
|Perrimon et al.
|1991
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000419	SYM 1 Ecol\lacZ<up>en.A</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 18 Jul 2001	RESZ 815
ID|FBtr0000419
SYM|Ecol\lacZ<up>en.A</up>RA
SYN|lacZ<up>en.A</up>RA
ASAL|<fbsym>FBal0041263==Ecol\lacZ<up>en.A</up></fbsym>
DT|18 Jul 2001
|10 Mar 1998
ID2|FBtr0000420
ASTP|<fbsym>FBtp0000310==P{en1}</fbsym>
|<fbsym>FBms0001023==enA::lacZ(6.9)</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0051851
|Kassis
|1990
RNAT|mRNA
BODP|Acts as enhancer trap: expression pattern dependent upon site of insertion.
ASM|transcript distribution deduced from reporter protein
}

REFDSR
{
RDID|FBrf0053745
|Perrimon et al.
|1991
RNAT|mRNA
BODP|Subcellular localization: cytoplamic.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t>  <a> cytoplasm <p>
}

REF
{
REFM|FBrf0051851
|Kassis
|1990
REFM|FBrf0053745
|Perrimon et al.
|1991
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000445	SYM 1 ovo<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 3	DT 1 7 Apr 1998	RESZ 4586
ID|FBtr0000445
SYM|ovo<up>+</up>R
ASAL|<fbsym>FBal0070857==ovo<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000446
ASGN|<fbsym>FBgn0003028==ovo</fbsym>

REFDSR
{
RDID|FBrf0053878
|Mevel-Ninio et al.
|1991
RNAT|mRNA
BODP|<fbsym>FBgn0003028==ovo</fbsym> transcript is detected at very low levels in stage 8 of oogenesis. By
| stage 10, it is present in nurse cells, predominantly in the cytoplasm, and
| at low levels in epithelial follicle cells. <fbsym>FBgn0003028==ovo</fbsym> is expressed at high
| levelsand uniformly in early embryogenesis, but by cellularization, the
| levels of transcript drop sharply. Instead, there is strong <fbsym>FBgn0003028==ovo</fbsym>
| expression in pole cells.
ASM|in situ
CVBODP|in situ
|<t> O | stage 8 <a> <p>
|<t> O,A | stage 10 <a> nurse cell <p>
|<t> O,A | stage 10 <a> follicle cell <p>
|<t> E | early <a>  <p> ubiquitous
|<t> E | cellular blastoderm <a>  <p> ubiquitous
|<t> E | cellular blastoderm <a> pole cell <p>
CC|The <fbsym>FBgn0003028==ovo</fbsym> transcript has at least 3 exons and 2 introns.
}

REFDSR
{
RDID|FBrf0076971
|Garfinkel et al.
|1994
RNAT|mRNA
BODP|<fbsym>FBgn0003028==ovo</fbsym> expression is ubiquitous in the syncytial blastoderm embryo, but
| becomes restricted to the posterior pole germ line precursor cells at
| cellular blastoderm stage. At late stage 13, <fbsym>FBgn0003028==ovo</fbsym> is expressed in a
| segmentally repeated pattern corresponding to the position of the ventral
| denticle belts. Additional staining is seen in the labial segment, the
| dorsal ridge, the stomatogastric ganglia, and the dorsal hairs. The
| germarium and early egg chamber have low levels of <fbsym>FBgn0003028==ovo</fbsym>, while the stage
| S10 nurse cell cytoplasm shows strong <fbsym>FBgn0003028==ovo</fbsym> transcript hybridization signal.
ASM|in situ
CVBODP|in situ
|<t> E | syncytial blastoderm <a>  <p> ubiquitous
|<t> E | cellular blastoderm <a> pole cell <p>
|<t> E | stage 13 | late <a> denticle belt <p> segmentally repeated
|<t> E | stage 10-11 <a> embryonic labial segment <p>
|<t> E | stage 13 | late <a> dorsal ridge <p>
|<t> E | stage 13 | late <a> stomatogastric nervous system <p>
|<t> E | stage 13 | late <a> dorsal hair <p><t> O <a> egg chamber | early <p>
|<t> O,A <a> germarium <p>
|<t> O,A | stage S10 <a> nurse cell | restricted <p>
CC|Three potential <fbsym>FBgn0003028==ovo</fbsym> mRNAs are detected on Northern blots, of 5.0, 7.1, and
| 2.7 kb. The 2.7 kb transcript might be a breakdown product of the 7.1 kb
| transcript. The 5.0 and 7.1 kb transcripts differ in their exon usage, as
| well as their polyadenylation sites.
}

REFDSR
{
RDID|FBrf0080251
|Mevel-Ninio et al.
|1995
RNAT|mRNA
BODP|<fbsym>FBgn0003028==ovo</fbsym> transcript is present at high levels in stage 1-2 embryos. By late
| stage 5, <fbsym>FBgn0003028==ovo</fbsym> transcript expression has become concentrated in pole cells,
| and pole cell expression is detected through stage 8, after which it
| disappearsuntil stage 17. At late stage 5, some <fbsym>FBgn0003028==ovo</fbsym> expression is also
| seen around somatic nuclei, especially in the region which will form the
| cephalic furrow, and by stage 6, <fbsym>FBgn0003028==ovo</fbsym> transcript expression is seen in two
| bands at 65-75% egg length and at 80-85% egg length. At stage 8, <fbsym>FBgn0003028==ovo</fbsym>
| expression is seen in the anterior border of the cephalic furrow, and by
| stage 10, staining is seen in the pharynx and antennal regions. By germ
| band retraction at late stage 12, an additional, segmented pattern of <fbsym>FBgn0003028==ovo</fbsym>
| transcript expression becomes visible in the anterior part of each
| abdominal and thoracic segment, which corresponds to the position of the
| denticle belt and dorsal hairs at stage 14. At stage 17, <fbsym>FBgn0003028==ovo</fbsym> transcript
| expression is restricted to the gonads.
ASM|in situ
CVBODP|in situ
|<t> E | stage 1-2 <a> <p> ubiquitous
|<t> E | stage 5-8 <a> pole cell <p>
|<t> E | stage 6 <a>  <p> 65-75% egg length
|<t> E | stage 6 <a>  <p> 80-85% egg length
|<t> E | stage 8 <a> cephalic furrow | restricted <p>
|<t> E | stage 10 <a> embryonic/larval pharynx <p>
|<t> E | stage 10 <a> antenna <p>
|<t> E | stage 12 | late <a>  <p> segmentally repeated
|<t> E | stage 12 | late <a> intercalary segment <p>
|<t> E | stage 14 <a> dorsal hair <p>
|<t> E | stage 14 <a> denticle belt | restricted <p>
|<t> E | stage 17 <a> gonad  <p>
}

REF
{
REFM|FBrf0053878
|Mevel-Ninio et al.
|1991
REFM|FBrf0076971
|Garfinkel et al.
|1994
REFM|FBrf0080251
|Mevel-Ninio et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000453	SYM 1 ph-p<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 2	DT 1 7 Apr 1998	RESZ 617
ID|FBtr0000453
SYM|ph-p<up>+</up>RA
ASAL|<fbsym>FBal0070880==ph-p<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000454
ASGN|<fbsym>FBgn0004861==ph-p</fbsym>
ASPP|<fbsym>FBpp0000995==ph-p-P1</fbsym>

REFDSR
{
RDID|FBrf0054014
|Deatrick et al.
|1991
RNAT|mRNA
CC|Transcripts of 6.4kb and 6.1kb are observed in the region (FBrf457872) but
| it's not clear if they are transcribed from <fbsym>FBgn0004861==ph-p</fbsym> or <fbsym>FBgn0004860==ph-d</fbsym>.
}

REFDSR
{
RDID|FBrf0056123
|DeCamillis et al.
|1992
RNAT|mRNA
}

REF
{
REFM|FBrf0054014
|Deatrick et al.
|1991
REFM|FBrf0056123
|DeCamillis et al.
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000461	SYM 1 Ecol\lacZ<up>GMR.A.hs</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 28 Jul 1999	RESZ 1508
ID|FBtr0000461
SYM|Ecol\lacZ<up>GMR.A.hs</up>RA
SYN|lacZ<up>GMR.A.hs</up>RA
|lacZ<up>ninaE.A.hs</up>RA
ASAL|<fbsym>FBal0041800==Ecol\lacZ<up>GMR.A.hs</up></fbsym>
DT|28 Jul 1999
|10 Mar 1998
ID2|FBtr0000463
|FBtr0000464
|FBtr0000462
ASTP|<fbsym>FBtp0001223==P{GMR-lacZ.A}</fbsym>
|<fbsym>FBmc0001214==pP{GMR-lacZ.A}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0054063
|Moses and Rubin
|1991
RNAT|mRNA
BODP|No expression in adult brain.
ASM|transcript distribution deduced from reporter protein
RNAT|mRNA
BODP|Reporter gene expression is observed in a three zone pattern in the eye
| imaginal disc. No expression is seen anterior to the furrow, weak
| expression begins in the furrow and extends posteriorly, and strong
| expression occurs from about the 8th column of developing ommatidia to the
| back of the disc. Expression occurs only in the photoreceptor cells.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar <a> eye-antennal disc | posterior <p>
|<t> L | third instar <a> morphogenetic furrow <p>
|<t> L | third instar <a> photoreceptor cell | presumptive <p>
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar <a> eye-antennal disc | posterior <p>
|<t> L | third instar <a> photoreceptor cell | presumptive <p>
|<t> L | third instar <a> larval brain <p>
|<t> A <a> retina <p>
|<t> A <a> ocellus<p>
}

REF
{
REFM|FBrf0054063
|Moses and Rubin
|1991
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000462	SYM 1 Ecol\lacZ<up>GMR.C.hs</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 28 Jul 1999	RESZ 2098
ID|FBtr0000462
SYM|Ecol\lacZ<up>GMR.C.hs</up>RA
SYN|lacZ<up>GMR.C.hs</up>RA
|lacZ<up>ninaE.38-1</up>RA
|lacZ<up>ninaE.C.hs</up>RA
ASAL|<fbsym>FBal0041801==Ecol\lacZ<up>GMR.C.hs</up></fbsym>
DT|28 Jul 1999
|10 Mar 1998
ID2|FBtr0000464
|FBtr0000465
|FBtr0000728
|FBtr0000729
|FBtr0000463
ASTP|<fbsym>FBtp0001226==P{GMR-lacZ.C(38.1)}</fbsym>
|<fbsym>FBmc0001217==pP{GMR-lacZ.C(38.1)}</fbsym>
ASGN|<fbsym>FBgn0014445==Scer\GAL4</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0054063
|Moses and Rubin
|1991
RNAT|mRNA
ASM|transcript distribution deduced from reporter protein
RNAT|mRNA
BODP|In the eye disc, reporter gene expression is found only in the posterior
| part of the disc where it is restricted to photoreceptor cells. Expression
| is also seen in the optic stalk and in Bolwig's nerve.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar <a> eye-antennal disc | posterior <p>
|<t> L <a> Bolwig's nerve <p>
|<t> L <a> optic stalk <p>
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar <a> eye-antennal disc | restricted <p>
|<t> L | third instar <a> morphogenetic furrow | posterior <p>
|<t> L | third instar <a> photoreceptor cell | presumptive <p>
}

REFDSR
{
RDID|FBrf0065382
|Ellis et al.
|1993
RNAT|mRNA
BODP|The reporter construct is expressed only in photoreceptor cells in the
| developing eye disc.
ASM|transcript distribution deduced from reporter protein
RNAT|mRNA
BODP|In third instar larva: expressed predominantly in photoreceptor cells in
| eye-antennal disc; also expressed in a small number of cells in the brain.
ASM|transcript distribution deduced from reporter protein
CVBODP|<t> L <a> photoreceptor cell | presumptive <p>
|transcript distribution deduced from reporter protein
|<t> L | third instar <a> eye-antennal disc <p>
|<t> L | third instar <a> photoreceptor cell | presumptive <p>
|<t> L | third instar <a> larval brain | restricted <p>
}

REF
{
REFM|FBrf0054063
|Moses and Rubin
|1991
REFM|FBrf0065382
|Ellis et al.
|1993
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000491	SYM 1 shi<up>+</up>RA	TRL 1 3.3	ASM 1 -	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 307
ID|FBtr0000491
SYM|shi<up>+</up>RA
ASAL|<fbsym>FBal0071044==shi<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000492
ASGN|<fbsym>FBgn0003392==shi</fbsym>

REFDSR
{
RDID|FBrf0054780
|van der Bliek and Meyerowitz
|1991
RNAT|mRNA
TRL|3.3
}

REF
{
REFM|FBrf0054780
|van der Bliek and Meyerowitz
|1991
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000523	SYM 1 sgg<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 2	DT 1 7 Apr 1998	RESZ 465
ID|FBtr0000523
SYM|sgg<up>+</up>RA
ASAL|<fbsym>FBal0071039==sgg<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000524
ASGN|<fbsym>FBgn0003371==sgg</fbsym>
ASPP|<fbsym>FBpp0001675==sgg<up>+</up>P496</fbsym>

REFDSR
{
RDID|FBrf0055543
|Siegfried et al.
|1992
RNAT|mRNA
}

REFDSR
{
RDID|FBrf0058144
|Ruel et al.
|1993
RNAT|mRNA
EXNSQ|3,4,6-8,9c
CC|represented by cDNA NB11
}

REF
{
REFM|FBrf0055543
|Siegfried et al.
|1992
REFM|FBrf0058144
|Ruel et al.
|1993
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000541	SYM 1 sas<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 1473
ID|FBtr0000541
SYM|sas<up>+</up>R
ASAL|<fbsym>FBal0071011==sas<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000542
ASGN|<fbsym>FBgn0002306==sas</fbsym>

REFDSR
{
RDID|FBrf0055816
|Schonbaum et al.
|1992
RNAT|mRNA
BODP|<fbsym>FBgn0002306==sas</fbsym> transcripts are expressed in all ectodermal tissues which produce a
| cuticle. Strong expression is observed in the hypoderm, pharynx,
| oesophagus, proventriculus, hindgut, and the trachea in stages 15 and 16.
| Expression begins early in the development of these tissues and is seen in
| the hypodermis, foregut and hindgut of stage 12 embyros. <fbsym>FBgn0002306==sas</fbsym> is expressed
| in third instar imaginal discs and in several imaginal-disc-derived tissues
| in adults including legs, wings, eyes, mouthparts, thoracic wall, and
| reproductive tract. Expression was also observed in the abdominal wall.
ASM|in situ
CVBODP|in situ
|<t> E | stage 12-16 <a> embryonic/larval foregut <p>
|<t> E | stage 12-16 <a> embryonic/larval hindgut <p>
|<t> E | stage 15-16 <a> embryonic/larval pharynx <p>
|<t> E | stage 15-16 <a> embryonic/larval oesophagus <p>
|<t> E | stage 15,16 <a> embryonic/larval proventriculus <p>
|<t> E | stage 15,16 <a> trachea <p>
|<t> E | stage 12-16 <a> epidermis <p>
|<t> L | third instar <a> imaginal disc <p>
|<t> A <a> leg <p>
|<t> A <a> wing <p>
|<t> A <a> eye <p>
|<t> A <a> mouthparts <p>
|<t> A <a> reproductive system <p>
}

REF
{
REFM|FBrf0055816
|Schonbaum et al.
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000549	SYM 1 pum<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 1295
ID|FBtr0000549
SYM|pum<up>+</up>R
ASAL|<fbsym>FBal0070931==pum<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000550
ASGN|<fbsym>FBgn0003165==pum</fbsym>
ASPP|<fbsym>FBpp0001076==pum<up>+</up>P1533</fbsym>

REFDSR
{
RDID|FBrf0055853
|MacDonald
|1992
RNAT|mRNA
EXNSQ|2-13
BODP|<fbsym>FBgn0003165==pum</fbsym> transcripts are first detected in the most mature portions of the
| germarium. They are detected throughout the egg chamber in stages S1-S5.
| <fbsym>FBgn0003165==pum</fbsym> transcripts are not present in intermediate stages but reappear at
| stage S9 atwhich time they are present in the nurse cells. <fbsym>FBgn0003165==pum</fbsym> RNA is
| transferred from nurse cells to the oocyte and are present in early
| embryos. Two patterns are seen in precellular blastoderm stage embryos. In
| some cases <fbsym>FBgn0003165==pum</fbsym> transcripts are spread throughout the embryo. In other
| cases, they are spread throughout but are further concentrated at the
| posterior pole and become associated with pole cells.
ASM|in situ
CVBODP|in situ
|<t> O,A <a> germarium <p>
|<t> O,A | stage >=S9 <a> border follicle cell <p>
|<t> E <a>  <p> ubiquitous
|<t> E <a> pole cell <p>
CC|It is not known to which transcript the cDNA corresponds.
}

REF
{
REFM|FBrf0055853
|MacDonald
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000559	SYM 1 Ecol\lacZ<up>Dpt.PR</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 863
ID|FBtr0000559
SYM|Ecol\lacZ<up>Dpt.PR</up>RA
SYN|lacZ<up>Dpt.PR</up>RA
ASAL|<fbsym>FBal0041171==Ecol\lacZ<up>Dpt.PR</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000560
ASTP|<fbsym>FBtp0004148==P{Dipt2.2-lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0055942
|Reichhart et al.
|1992
RNAT|mRNA
BODP|Reporter gene expression is induced in response to injection of complete
| Freund's adjuvant in late third instar larvae (96-120hr). Younger animals
| do not express the reporter gene in response to the injection. From
| pupariation on, there is a gradual decrease in the response to the
| challenge. In response to live bacteria, a faint response is seen in second
| instar larvae and a full response is seen in adults.
ASM|transcript distribution deduced from reporter protein
}

REF
{
REFM|FBrf0055942
|Reichhart et al.
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000567	SYM 1 otu<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 357
ID|FBtr0000567
SYM|otu<up>+</up>RA
ASAL|<fbsym>FBal0070856==otu<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000568
ASGN|<fbsym>FBgn0003023==otu</fbsym>
ASPP|<fbsym>FBpp0001680==otu<up>+</up>P853</fbsym>

REFDSR
{
RDID|FBrf0056128
|Steinhauer and Kalfayan
|1992
RNAT|mRNA
EXNSQ|1-6,6a,7,8
}

REF
{
REFM|FBrf0056128
|Steinhauer and Kalfayan
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000584	SYM 1 dsx<up>+</up>R	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 656
ID|FBtr0000584
SYM|dsx<up>+</up>R
ASAL|<fbsym>FBal0068854==dsx<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000585
ASGN|<fbsym>FBgn0000504==dsx</fbsym>

REFDSR
{
RDID|FBrf0057558
|Inoue et al.
|1992
RNAT|mRNA
CC|Six tandemly interspersed repeats of 13-nucleotide sequences (TC (T/A) (T/A)
| C (A/G) ATCAACA), in the female-specific fourth exon are necessary for
| female-specific splicing of <fbsym>FBgn0000504==dsx</fbsym> pre-mRNA. The A-, B- and C- type motifs
| function efficiently as cis elements to promote the female-specific
| splicing of <fbsym>FBgn0000504==dsx</fbsym> pre-mRNA in cells.
}

REF
{
REFM|FBrf0057558
|Inoue et al.
|1992
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000605	SYM 1 Ecol\lacZ<up>Uch-A</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 601
ID|FBtr0000605
SYM|Ecol\lacZ<up>Uch-A</up>RA
SYN|lacZ<up>Uch-A</up>RA
ASAL|<fbsym>FBal0042205==Ecol\lacZ<up>Uch-A</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000606
ASTI|<fbsym>FBti0003567==P{A92}A</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0058042
|Zhang et al.
|1993
RNAT|mRNA
BODP|Reporter gene expression is observed in nurse cells and oocytes.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> O,A <a> nurse cell <p>
|<t> O,A <a> oocyte <p>
}

REF
{
REFM|FBrf0058042
|Zhang et al.
|1993
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000615	SYM 1 Ecol\lacZ<up>Rop.P</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 1400
ID|FBtr0000615
SYM|Ecol\lacZ<up>Rop.P</up>RA
SYN|lacZ<up>Rop.P</up>RA
ASAL|<fbsym>FBal0041896==Ecol\lacZ<up>Rop.P</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000616
ASTP|<fbsym>FBtp0004437==P{lacZ<up>Rop.P</up>}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0058072
|Salzberg et al.
|1993
RNAT|mRNA
BODP|Reporter gene expression is observed in all the cells of the larval salivary
| glands. A highly specific, segmentally repeated pattern of staining was
| observed in the larval CNS, which is identical to that seen with a <fbsym>FBgn0003206==Ras64B</fbsym>
|-<fbsym>FBgn0014447==Ecol\lacZ</fbsym> line. Staining is limited to ganglion mother cells
| and cell that have already completed their divisions. In adult males,
| expression is observed in the testis in cyst cells. In the female
| reproductive system, staining is apparent in all cells including nurse
| cells, follicle cells and the oocytes.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> L <a> embryonic/larval salivary gland <p>
|<t> L <a> larval central nervous system <p>
|<t> A,S <a> testis <p>
|<t> S,A <a> cyst cell <p>
|<t> O,A | female <a> ovary <p>
|<t> O,A <a> nurse cell <p>
|<t>O,A <a> oocyte <p>
|<t> O,A <a> follicle cell <p>
ASCRGN|<fbsym>FBgn0004574==Rop</fbsym>
}

REF
{
REFM|FBrf0058072
|Salzberg et al.
|1993
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000617	SYM 1 Psc<up>+</up>R	TRL 1 -	ASM 1 radioisotope in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 826
ID|FBtr0000617
SYM|Psc<up>+</up>R
ASAL|<fbsym>FBal0068204==Psc<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000618
ASGN|<fbsym>FBgn0005624==Psc</fbsym>

REFDSR
{
RDID|FBrf0058093
|Martin and Adler
|1993
RNAT|mRNA
BODP|<fbsym>FBgn0005624==Psc</fbsym> is expressed in the central nervous system, and in all imaginal discs
| of third instar larvae. In 24 hour pupae, <fbsym>FBgn0005624==Psc</fbsym> transcript is found in the
| epidermis, brain, and the nerve cord. In adult females, <fbsym>FBgn0005624==Psc</fbsym> isexpressed
| in the ovary.
ASM|radioisotope in situ
CVBODP|radioisotope in situ
|<t> L | third instar <a> larval central nervous system <p>
|<t> L | third instar <a> imaginal disc <p>
|<t> P | 24 hr <a> adult brain <p>
|<t> O,A | female <a> ovary <p>
}

REF
{
REFM|FBrf0058093
|Martin and Adler
|1993
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000621	SYM 1 Ecol\lacZ<up>nau.PP</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 14 May 1999	RESZ 1630
ID|FBtr0000621
SYM|Ecol\lacZ<up>nau.PP</up>RA
SYN|lacZ<up>nau.PP</up>
|lacZ<up>nau.PP</up>RA
ASAL|<fbsym>FBal0041789==Ecol\lacZ<up>nau.PP</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000511
|FBtr0000622
|FBtr0000510
ASTP|<fbsym>FBtp0004419==P{nau-lacZ.P}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0054970
|Paterson et al.
|1991
RNAT|mRNA
BODP|The pattern of <fbsym>FBgn0014447==Ecol\lacZ</fbsym> reporter gene staining mimics the pattern of
| nuclear staining seen with the <fbsym>FBgn0002922==nau</fbsym> antibody.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E | stage >=11 <a>  <p> segmentally repeated
|<t> E | stage >=11 <a> myoblast <of> larval muscle system <p>
|<t> E | stage >=14 <a> ventral oblique muscle <p>
|<t> E | stage >=14 <a>  <p> segmentallyrepeated
|<t> E | stage >=14 <a> abdominal 1..7 ventral oblique muscle 4 <p>
|<t> E | stage >=14 <a> abdominal 1..7 ventral oblique muscle 5 <p>
|<t> E | stage >=14 <a> abdominal 2..7 ventral oblique muscle 6 <p>
|<t> E | stage >=14 <a> abdominal 1 ventral acute muscle 1 <p>
|<t> E | stage >=14 <a> abdominal 1 ventral longitudinal muscle 1 <p>
|<t> E | stage >=14 <a> pharyngeal muscle <p>
|<t> E | stage >=14 <a> anterior spiracle retractor muscle <p>
|<t> E | stage >=14 <a> muscle fibre <of> telson <p>
ASCRGN|<fbsym>FBgn0002922==nau</fbsym>
}

REFDSR
{
RDID|FBrf0058097
|Shishido et al.
|1993
RNAT|mRNA
ASM|transcript distribution deduced from reporter protein
}

REF
{
REFM|FBrf0054970
|Paterson et al.
|1991
REFM|FBrf0058097
|Shishido et al.
|1993
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000633	SYM 1 neur<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 3	DT 1 16 Sep 1998	RESZ 2992
ID|FBtr0000633
SYM|neur<up>+</up>R
ASAL|<fbsym>FBal0070803==neur<up>+</up></fbsym>
DT|16 Sep 1998
|10 Mar 1998
ID2|FBtr0000634
ASGN|<fbsym>FBgn0002932==neur</fbsym>
ASPP|<fbsym>FBpp0003538==neur-P1</fbsym>

REFDSR
{
RDID|FBrf0053887
|Boulianne et al.
|1991
RNAT|mRNA
BODP|In the early embryo, <fbsym>FBgn0002932==neur</fbsym> is expressed in the ectoderm and the
| mesectoderm/mesoderm. Between 3-9 hr of embryogenesis, expression is
| detected in epidermoblasts and neuroblasts. In larval wing imaginal discs,
| <fbsym>FBgn0002932==neur</fbsym> is expressedin sensory organ precursor cells. Expression is also
| detected in the eye-imaginal disc, strongly on the posterior side of the
| morphogenetic furrow. In the central nervous system, expression is in
| proliferative centers, such as the inner and outer optic anlage of the
| brain, and the neuroblasts in the thoracic segments of the larval ventral ganglion.
ASM|in situ
CVBODP|in situ
|<t> E | early <a> mesoderm<p>
|<t> E | early <a> mesectoderm <p>
|<t> E | early <a> ectoderm <p>
|<t> E | 3-9 hr <a> neuroblast <p>
|<t> E | 3-9 hr <a> epidermoblast <p>
|<t> L | third instar stage 2 <a> sensillum precursor <of> dorsal mesothoracic disc <p>
|<t> L | third instar stage 2 <a> inner optic anlagen <p>
|<t> L | third instar stage 2 <a> outer optic anlagen <p>
|<t> L | third instar stage 2 <a> adult neuroblast <p>
|<t> L | third instar stage 2 <a> eye-antennal disc | restricted <p>
}

REFDSR
{
RDID|FBrf0058153
|Price et al.
|1993
RNAT|mRNA
BODP|Before cellularization, <fbsym>FBgn0002932==neur</fbsym> transcript is detected uniformly across the
| embryo. After the cellular blastoderm stage, the <fbsym>FBgn0002932==neur</fbsym> transcript is
| expressed in the presumptive mesoderm, first in a patchy pattern, then
| uniformly. Around the time of ventral furrow formation (stage 6) <fbsym>FBgn0002932==neur</fbsym>
| expression is weakly detected in a transverse stripe pattern. With the
| closure of the ventral furrow, <fbsym>FBgn0002932==neur</fbsym>-expressing cells are internalized.
| <fbsym>FBgn0002932==neur</fbsym> transcript is distributed uniformly in the neurectoderm of stage 9
| embryos; by stage 10, neuroblasts have slightly elevated levels of <fbsym>FBgn0002932==neur</fbsym>
| transcript in comparison to their neighbors. Clusters of cells in the
| presumptive lateral epidermis also express the <fbsym>FBgn0002932==neur</fbsym> transcript at stage
| 10. By stage 11, ventral and lateral epidermal <fbsym>FBgn0002932==neur</fbsym> transcript levels
| decline, although <fbsym>FBgn0002932==neur</fbsym> transcript persists in some neural cells later in embryogenesis.
ASM|in situ
CVBODP|in situ
|<t> E | stage 5 <a> mesoderm | presumptive <p>
|<t> E | stage 9 <a> neurectoderm <p>
|<t> E | stage 10 <a> neuroblast <p>
}

REFDSR
{
RDID|FBrf0058155
|Boulianne et al.
|1993
RNAT|mRNA
}

REF
{
REFM|FBrf0053887
|Boulianne et al.
|1991
REFM|FBrf0058153
|Price et al.
|1993
REFM|FBrf0058155
|Boulianne et al.
|1993
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000652	SYM 1 tws<up>+</up>RA	TRL 1 -	ASM 1 northern blot	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 729
ID|FBtr0000652
SYM|tws<up>+</up>RA
ASAL|<fbsym>FBal0071441==tws<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000653
ASGN|<fbsym>FBgn0004889==tws</fbsym>
ASPP|<fbsym>FBpp0001462==tws-P2</fbsym>

REFDSR
{
RDID|FBrf0058530
|Uemura et al.
|1993
RNAT|mRNA
EXNSQ|3-7
BODP|<fbsym>FBgn0004889==tws</fbsym> transcripts are expressed ubiquitously in wing discs. They are also
| expressed in the eye-antennal disc, leg discs, and the CNS.
ASM|northern blot
|in situ
CVBODP|northern blot
|<t> L | third instar <a>  <p>
|in situ
|<t> L <a> dorsal mesothoracic disc <p>
|<t> L <a> ventral thoracic disc <p>
|<t> L <a> eye-antennal disc <p>
|<t> L <a> larval central nervous system <p>
}

REF
{
REFM|FBrf0058530
|Uemura et al.
|1993
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000699	SYM 1 Sxl<up>+</up>RA	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 571
ID|FBtr0000699
SYM|Sxl<up>+</up>RA
ASAL|<fbsym>FBal0068426==Sxl<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000700
ASGN|<fbsym>FBgn0003659==Sxl</fbsym>

REFDSR
{
RDID|FBrf0064442
|Erickson and Cline
|1993
RNAT|mRNA
BODP|<fbsym>FBgn0003659==Sxl</fbsym> transcripts are first detected at nuclear cycle 12, increase in
| abundance in female embryos during cycles 13 and 14, peak early in cycle
| 14, and start to decay at the end of cycle 14.
ASM|in situ
CVBODP|in situ
|<t> E | embryonic cycle 12-14 <a>  <p>
}

REF
{
REFM|FBrf0064442
|Erickson and Cline
|1993
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000702	SYM 1 Ecol\lacZ<up>Sxl.Pe</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 431
ID|FBtr0000702
SYM|Ecol\lacZ<up>Sxl.Pe</up>RA
SYN|lacZ<up>Sxl.Pe</up>RA
ASAL|<fbsym>FBal0041988==Ecol\lacZ<up>Sxl.Pe</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000703
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0064442
|Erickson and Cline
|1993
RNAT|mRNA
ASM|transcript distribution deduced from reporter protein
ASCRGN|<fbsym>FBgn0003659==Sxl</fbsym>
}

REF
{
REFM|FBrf0064442
|Erickson and Cline
|1993
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000790	SYM 1 Ecol\lacZ<up>Gld.pal+</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 30 Jun 1999	RESZ 818
ID|FBtr0000790
SYM|Ecol\lacZ<up>Gld.pal+</up>RA
SYN|lacZ<up>Gld.pal+.hs</up>RA
ASAL|<fbsym>FBal0055537==Ecol\lacZ<up>Gld.pal+</up></fbsym>
DT|30 Jun 1999
|10 Mar 1998
ID2|FBtr0000791
ASTP|<fbsym>FBtp0001367==P{-425bpGld/lacZ}</fbsym>
|<fbsym>FBmc0001348==pP{-425bpGld/lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0068515
|Gunaratne et al.
|1994
RNAT|mRNA
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar <a> embryonic/larval pharynx <p>
|<t> L | third instar <a> anterior spiracular gland <p>
|<t> L | third instar <a> larval hypodermal muscle <p>
|<t> L | third instar <a> antenno-maxillary complex <p>
|<t> A | male <a> ejaculatory duct <p>
}

REF
{
REFM|FBrf0068515
|Gunaratne et al.
|1994
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000791	SYM 1 Ecol\lacZ<up>Gld.pal</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 30 Jun 1999	RESZ 596
ID|FBtr0000791
SYM|Ecol\lacZ<up>Gld.pal</up>RA
SYN|lacZ<up>Gld.pal.hs</up>RA
ASAL|<fbsym>FBal0055538==Ecol\lacZ<up>Gld.pal</up></fbsym>
DT|30 Jun 1999
|10 Mar 1998
ID2|FBtr0000792
ASTP|<fbsym>FBtp0006571==P{Gpal-lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0068515
|Gunaratne et al.
|1994
RNAT|mRNA
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> A | male <a> ejaculatory bulb <p>
|<t> L | third instar <a> anterior spiracular gland <p>
}

REF
{
REFM|FBrf0068515
|Gunaratne et al.
|1994
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000792	SYM 1 Ecol\lacZ<up>Gld.palmut</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 30 Jun 1999	RESZ 681
ID|FBtr0000792
SYM|Ecol\lacZ<up>Gld.palmut</up>RA
SYN|lacZ<up>Gld.palmut.hs</up>RA
ASAL|<fbsym>FBal0055539==Ecol\lacZ<up>Gld.palmut</up></fbsym>
DT|30 Jun 1999
|10 Mar 1998
ID2|FBtr0000793
ASTP|<fbsym>FBtp0006572==P{Gpal(mut)-lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0068515
|Gunaratne et al.
|1994
RNAT|mRNA
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar <a> embryonic/larval pharynx <p>
|<t> L | third instar <a> larval hypodermal muscle <p>
|<t> L | third instar <a> antenno-maxillary complex <p>
}

REF
{
REFM|FBrf0068515
|Gunaratne et al.
|1994
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000801	SYM 1 Ecol\lacZ<up>sna.NB</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 25 Jan 2001	RESZ 952
ID|FBtr0000801
SYM|Ecol\lacZ<up>sna.NB</up>RA
SYN|Ecol\lacZ<up>sna.NB</up>R
|lacZ<up>sna.NB</up>R
ASAL|<fbsym>FBal0041972==Ecol\lacZ<up>sna.NB</up></fbsym>
DT|25 Jan 2001
|10 Mar 1998
ID2|FBtr0000802
ASTP|<fbsym>FBtp0004469==P{NB}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0068539
|Ip et al.
|1994
RNAT|mRNA
BODP|When as little as 0.25 kb of sequence immediately upstream of <fbsym>FBgn0003448==sna</fbsym> is
| deleted in a <fbsym>FBgn0003448==sna</fbsym>-promoter driven <fbsym>FBgn0014447==Ecol\lacZ</fbsym> constuct, reporter
| expression is abolished in the PNS and CNS, and severely reduced in the
| mesoderm. This suggests that an augmentation element resides within the
| 0.25 kb segment.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> mesoderm <p>
ASCRGN|<fbsym>FBgn0003448==sna</fbsym>
}

REF
{
REFM|FBrf0068539
|Ip et al.
|1994
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000825	SYM 1 tkv<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 3	DT 1 14 Jun 2000	RESZ 3758
ID|FBtr0000825
SYM|tkv<up>+</up>R
SYN|tvk<up>+</up>R
|unnamed
ASAL|<fbsym>FBal0071387==tkv<up>+</up></fbsym>
DT|14 Jun 2000
|10 Mar 1998
ID2|FBtr0005395
|FBtr0000826
ASGN|<fbsym>FBgn0003716==tkv</fbsym>
ASPP|<fbsym>FBpp0001786==tkv<up>+</up>P</fbsym>

REFDSR
{
RDID|FBrf0072460
|Affolter et al.
|1994
RNAT|mRNA
BODP|High uniform expression of <fbsym>FBgn0003716==tkv</fbsym> transcripts is observed in unfertilized
| eggs. During cellularization, the pattern is very dynamic. With the
| exception of two small gaps, transcripts accumulate along the entire dorsal
| side of the embryo. During the late phase of cellularization, transcripts
| accumulate along the ventral side of the embryo. <fbsym>FBgn0003716==tkv</fbsym> transcripts are
| expressed in the mesoderm during mesoderm invagination and during germ band
| extension. Expression is next observed in the medial ectodermal region in
| the neurectoderm, with lower levels detected toward the midline. In stage
| 11, transcripts are expressed in the tracheal placodes. Shortly after, the
| continuous stripe of expression along the anteroposterior axis in the
| ventrolateral ectoderm is split in a segmentally repeated manner. In stage
| 13, transcripts are detected in parts of the visceral mesoderm. At stage
| 15, the sections of visceral mesoderm that express <fbsym>FBgn0003716==tkv</fbsym> are located just
| anterior to and posterior to the developing gastric caeca and in the
| posterior part of the midgut. <fbsym>FBgn0003716==tkv</fbsym> is also expressed in a complex pattern
| in the head region.
ASM|in situ
CVBODP|in situ
|<t> E | stage 5 <a> epidermis | dorsal <p>
|<t> E | stage 6-9 <a> mesoderm <p>
|<t> E | stage 11 <a> tracheal placode <p>
|<t> E | stage >12 <a> visceral mesoderm <p>
}

REFDSR
{
RDID|FBrf0076484
|Okano et al.
|1994
RNAT|mRNA
BODP|Ubiquitous expression of <fbsym>FBgn0003716==tkv</fbsym> is observed in embryonic stages 1-2.
| Expression is also ubiquitous in stages 3-4 but a slight dorso-ventral
| gradient is observed at this time. Levels begin to decrease at
| cellularization, yielding an asymmetrictranscript distribution, with the
| highest levels remaining on the dorsal side. At the beginning of
| gastrulation, expression is observed in the invaginating mesoderm and in a
| pair-rule pattern in the ectoderm. High and localized expression of <fbsym>FBgn0003716==tkv</fbsym>
| in the mesoderm is seen during germ band extension. By stage 10, expression
| is high in the entire anlagen of the germ band in the mesoderm. At stage
| 11, expression is apparent in a segmental pattern in the tracheal pits.
| After germ band retraction, expression in the mesoderm begins to withdraw.
| Expression is observed in the midgut from stage 12. At stage 16, a high
| level of expression is observed in the chambers of the first and fourth
| midgut constrictions.
ASM|in situ
CVBODP|in situ
|<t> E | early <a>  <p> ubiquitous
|<t> E | stage 3,4 <a>  <p> dorsal ventral gradient
|<t> E | stage <a>  <p>
|<t> E | stage 6-12 <a> mesoderm <p>
|<t> E | stage 6 <a> <p> pair-rule
|<t> E | stage 11 <a> tracheal pit <p>
|<t> E | stage >=12 <a> posterior midgut primordium <p>
|<t> E | stage >=12 <a> anterior midgut primordium <p>
|<t> E | stage 12-17 <a> embryonic/larval midgut <p>
|<t> E <a> midgut constriction 1 <p>
|<t> E <a> midgut constriction 4 <p>
}

REFDSR
{
RDID|FBrf0104902
|Haerry et al.
|1998
RNAT|mRNA
BODP|The <fbsym>FBgn0003716==tkv</fbsym> transcript is expressed at high levels in the pleural regions and
| the hinge region of the wing disc.
ASM|in situ
CVBODP|<t> L | third instar <a> dorsal mesothoracic disc | restricted <p>
}

REF
{
REFM|FBrf0072460
|Affolter et al.
|1994
REFM|FBrf0076484
|Okano et al.
|1994
REFM|FBrf0104902
|Haerry et al.
|1998
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000856	SYM 1 chic<up>+</up>R	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 30 Jun 1999	RESZ 478
ID|FBtr0000856
SYM|chic<up>+</up>R
SYN|chi<up>+</up>R
ASAL|<fbsym>FBal0097450==chic<up>+</up></fbsym>
DT|30 Jun 1999
|10 Mar 1998
ID2|FBtr0000857
ASGN|<fbsym>FBgn0000308==chic</fbsym>

REFDSR
{
RDID|FBrf0073018
|Edwards et al.
|1994
RNAT|mRNA
CC|Overexpression of the <fbsym>FBgn0020863==chi</fbsym> cDNA in fission yeast causes inhibition of cell
| division and complete disruption of cell shape and of the actin cytoskeleton.
}

REF
{
REFM|FBrf0073018
|Edwards et al.
|1994
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000899	SYM 1 Ten-m<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 2	DT 1 14 Nov 2001	RESZ 2535
ID|FBtr0000899
SYM|Ten-m<up>+</up>R
ASAL|<fbsym>FBal0068449==Ten-m<up>+</up></fbsym>
DT|14 Nov 2001
|10 Mar 1998
ID2|FBtr0000900
ASGN|<fbsym>FBgn0004449==Ten-m</fbsym>
ASPP|<fbsym>FBpp0001371==Ten-m<up>+</up>P2515</fbsym>

REFDSR
{
RDID|FBrf0073721
|Levine et al.
|1994
RNAT|mRNA
BODP|A segmentally repeated pattern of <fbsym>FBgn0004449==Ten-m</fbsym> transcript expression becomes
| visible at 5.5-7.5 hours of embyrogenesis. At 9.5-10 hours, the cell bodies
| of a subset of cells in the central nervous system express <fbsym>FBgn0004449==Ten-m</fbsym>
| transcript ina segmentally repeated pattern.
ASM|in situ
CVBODP|in situ
|<t> E | 5.5-7.5 hr <a>  <p> segmentally repeated
|<t> E | 9.5 hr <a> embryonic central nervous system <p>
CC|The sizes of the two <fbsym>FBgn0004449==Ten-m</fbsym> transcripts are given as approximately 10 and
| 11 kb, which is in good agreement with the sizes of the two transcripts
| described in FBrf0075161.
}

REFDSR
{
RDID|FBrf0075161
|Baumgartner et al.
|1994
RNAT|mRNA
|mRNA
BODP|<fbsym>FBgn0004449==Ten-m</fbsym> transcripts are first detected in stage 5 embryos, where it is
| expressed in most regions, with the exception of the anterior and posterior
| poles. This pattern persists until early germ band extension, when 14
| stripes become visible inthe mesoderm and ectoderm. The presumptive cardiac
| cells and lymph glands stain at stage 12, and after germ band retraction at
| stage 13, additional signal is visible in the posterior spiracles, trachea,
| ventral cord, hemocytes and the supraoesophageal ganglion. At hatching,
| <fbsym>FBgn0004449==Ten-m</fbsym> transcripts are only detected in the ventral cord and brain. During
| larval and pupal stages, the ventral cord and brain, as well as the
| imaginal discs stain weakly for <fbsym>FBgn0004449==Ten-m</fbsym> transcripts, but the eye imaginal
| disc shows higher levels of expression during pupal stages.
ASM|in situ
CVBODP|in situ
|<t> E | stage 5-8 <a>  <p>
|<t> E | stage 10 <a>  <p>
|<t> E | stage 12 <a>  <p>
|<t> E | stage 12-13 <a> cardioblast <p>
|<t> E | stage 12-13 <a> lymph gland <p>
|<t> E | stage 13 <a> supraoesophageal ganglion <p>
|<t> E | stage 13 <a> ventral nerve cord <p>
|<t> E | stage 13 <a> posterior spiracle primordium <p>
|<t> E | stage 13 <a> trachea <p>
|<t> L-P <a> ventral nerve cord <p>
|<t> L-P <a> imaginal disc <p>
CC|Overlapping genomic and cDNA clones were sequenced to obtain a composite sequence.
}

REF
{
REFM|FBrf0073721
|Levine et al.
|1994
REFM|FBrf0075161
|Baumgartner et al.
|1994
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000918	SYM 1 ey<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 1735
ID|FBtr0000918
SYM|ey<up>+</up>R
ASAL|<fbsym>FBal0068925==ey<up>+</up></fbsym>
DT|23 Jul 2001
|10 Mar 1998
ID2|FBtr0000919
ASGN|<fbsym>FBgn0005558==ey</fbsym>

REFDSR
{
RDID|FBrf0074219
|Quiring et al.
|1994
RNAT|mRNA
BODP|<fbsym>FBgn0005558==ey</fbsym> is expressed in the embryonic central nervous system and in the
| eye-antennal disc primordia. In third instar larvae, <fbsym>FBgn0005558==ey</fbsym> transcript
| localizes to the anterior portion of the eye-antennal disc.
ASM|in situ
CVBODP|in situ
|<t> E <a> embryonic central nervous system <p>
|<t> E <a> eye-antennal disc | primordium <p>
|<t> L | third instar <a> eye-antennal disc | anterior <p>
}

REFDSR
{
RDID|FBrf0093719
|Sheng et al.
|1997
RNAT|mRNA
BODP|Levels of <fbsym>FBgn0005558==ey</fbsym> transcript decrease and are barely detectable by the end of
| the first half of pupal development. Levels subsequently increase and reach
| adult levels immediately after eclosion. <fbsym>FBgn0005558==ey</fbsym> transcripts are present at
| higher levels in wild-type flies compared to <fbsym>cli</fbsym> flies, indicating that
| the majority of <fbsym>FBgn0005558==ey</fbsym> transcript is localized to the compound eyes.
| Expression of <fbsym>FBgn0005558==ey</fbsym> transcript during Bolwig's organ (BO) development was
| studied. <fbsym>FBgn0005558==ey</fbsym> is expressed in BO precursors in stage 12 embryos, is absent
| in stage 13 to mid-stage 16 embryos, and is expressed in all BO cells in
| late stage 16-17 embryos.
CVBODP|<t> A <a> adult head <p>
|<t> P <a> <p>
|<t> E | stage 12 <a> embryonic Bolwig's organ <p>
|<t> E | stage >=16 |mid <a> embryonic Bolwig's organ <p>
}

REF
{
REFM|FBrf0074219
|Quiring et al.
|1994
REFM|FBrf0093719
|Sheng et al.
|1997
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000984	SYM 1 nub<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 3	DT 1 28 Jul 1999	RESZ 3629
ID|FBtr0000984
SYM|nub<up>+</up>R
ASAL|<fbsym>FBal0073963==nub<up>+</up></fbsym>
DT|28 Jul 1999
|10 Mar 1998
ID2|FBtr0001994
|FBtr0001995
|FBtr0000985
ASGN|<fbsym>FBgn0002970==nub</fbsym>
ASPP|<fbsym>FBpp0000927==nub-P1</fbsym>

REFDSR
{
RDID|FBrf0054628
|Lloyd and Sakonju
|1991
RNAT|mRNA
AGT|<fbsym>BX-C<up>-</up> | Df(3R)P9</fbsym>
|<fbsym>AS-C<up>-</up> | ?</fbsym>
|<fbsym>FBal0005403==hb<up>12</up></fbsym>
|<fbsym>FBal0004816==ftz<up>11</up></fbsym>
BODP|<fbsym>FBgn0002970==nub</fbsym> expression initiates at the cellular blastoderm stage in two bands at
| parasegments 7 and 11. Expression in the posterior stripe is stronger.
| During gastrulation, expression occurs in a segment polarity pattern with
| alternating wide and narrow stripes. In germband extended embryos, <fbsym>FBgn0002970==nub</fbsym> is
| expressed in selected CNS neurons and their support cells. CNS expression
| is stronger in T1-T3 and A8 than in A1-A7. Expression is also seen in some
| lateral and dorsal clusters of PNS cells, in the ligament cells of the
| chordotonal organs, and in two types of neurons (bipolar dendrite neurons
| and dendritic arbor cells). Expression patterns were observed in AS-C,
| BX-C, <fbsym>FBgn0000014==abd-A</fbsym>, <fbsym>FBgn0001180==hb</fbsym>, and <fbsym>FBgn0001077==ftz</fbsym> mutants. The mutant studies helped to
| establish the identities of PNS and CNS expressing cells and suggested
| regulatory interactions.
ASM|in situ
CVBODP|<t> E | cellular blastoderm <a> parasegment 7 <p>
|<t> E | cellular blastoderm <a> parasegment 11 <p>
|<t> E | stage 6 <a>  <p> odd pair-rule
|<t> E | stage 9 <a>  <p> segment polarity
|<t> E | late <a> larval labral sense organ | presumptive <p>
|<t> E | late<a> hypophysis <p>
|<t> E | late <a> embryonic peripheral nervous system | restricted <p>
|<t> E | late <a> central nervous system | restricted <p>
|<t> E | late <a> scolopidial ligament cell <of> lateral abdominal cluster <of> abdominal segment 1..7 <p>
|<t> E | late <a> bipolar dendrite neuron <of> dorsal abdominal cluster <of> abdominal segment 1..7 <p>
|<t> E | late <a> dendritic arborising neuron <of> dorsal abdominal cluster <of> abdominal segment 1..7 <p>
|<t> E | late <a> bipolar dendrite neuron <of> dorsal thoracic cluster <of> thoracic segment 2..3 <p>
|<t> E | late <a> scolopidial ligament cell <of> dorsal thoracic cluster <of> thoracic segment 2..3 <p>
|<t> E | late <a> chordotonal organ <of> lateral thoracic cluster <of> prothoracic segment <p>
|<t> E | late <a> peripheral nervous system <of> abdominal segment 8..9 <p>
}

REFDSR
{
RDID|FBrf0057550
|Prakash et al.
|1992
RNAT|mRNA
}

REFDSR
{
RDID|FBrf0076143
|Ng et al.
|1995
RNAT|mRNA
BODP|<fbsym>FBgn0002970==nub</fbsym> transcripts are expressed in the developing wing primordia beginning
| in the second larval instar In the third instar the expression domain fills
| the wing pouch. In the everted disc, <fbsym>FBgn0002970==nub</fbsym> expression fills the wing blade
| andpart of the hinge region. <fbsym>FBgn0002970==nub</fbsym> is also expressed in the corresponding
| region of the haltere and in a series of faint rings in the leg discs.
ASM|in situ
CVBODP|in situ
|<t> L <a> dorsal mesothoracic disc <p>
|<t> L <a> dorsal metathoracic disc <p>
|<t> L <a> ventral thoracic disc <p>
CC|cDNA characterization revealed two different forms of <fbsym>FBgn0002970==nub</fbsym> transcript which
| differ in their first exon and are predicted to produce two proteins which
| differ in their amino termini.
}

REF
{
REFM|FBrf0054628
|Lloyd and Sakonju
|1991
REFM|FBrf0057550
|Prakash et al.
|1992
REFM|FBrf0076143
|Ng et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000987	SYM 1 fz<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 7 Apr 1998	RESZ 1926
ID|FBtr0000987
SYM|fz<up>+</up>R
ASAL|<fbsym>FBal0069190==fz<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0000988
ASGN|<fbsym>FBgn0001085==fz</fbsym>
SK|FBst1001775
|Df(Y;2;3)D-4rv42/fz[613];  Dp(3;4)D-4rv42, fz[+]/+
|Total=1

REFDSR
{
RDID|FBrf0076154
|Park et al.
|1994
RNAT|mRNA
BODP|<fbsym>FBgn0001085==fz</fbsym> transcripts are only detected in ovaries in adult females and are not
| detected in males. They are uniformly distributed in early embryos. In
| third instar larvae, they are expressed in all imaginal discs and in the
| brain, ventral nerve cord, and proventriculus. In pupal sections,
| hybridization was seen in all regions of the epidermis and in the CNS.
| Whole mounts of wing showed hybridization across the entire wing.
ASM|radioisotope in situ
CVBODP|radioisotope in situ
|<t> O,A | female <a> ovary <p>
|<t> E | early <a>  <p> ubiquitous
|<t> L | third instar <a> imaginal disc <p>
|<t> L | third instar <a> larval brain <p>
|<t> L | third instar <a> ventral nerve cord <p>
|<t> L | third instar <a> embryonic/larval proventriculus <p>
|<t> P <a> epidermis <p>
|<t> P <a> central nervous system <p>
|<t> P <a> wing <p>
}

REFDSR
{
RDID|FBrf0084528
|Zheng et al.
|1995
RNAT|mRNA
BODP|<fbsym>FBgn0001085==fz</fbsym> transcripts are detected uniformly anterior to the morphogenetic
| furrow. Immediately anterior to the furrow, the level of expression sharply
| increases in a narrow band of cells. Staining intensity is decreased in the
| furrow and becomes intense immediately posterior to the furrow. The level
| of <fbsym>FBgn0001085==fz</fbsym> transcripts decreases to a low level about 6 rows posterior to the
| furrow. In the regions of expression, the level is uniform from the dorsal
| to ventral poles.
ASM|in situ
CVBODP|in situ
|<t> L <a> morphogenetic furrow <p>
|<t> L <a> eye-antennal disc <p>
}

REF
{
REFM|FBrf0076154
|Park et al.
|1994
REFM|FBrf0084528
|Zheng et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000991	SYM 1 Ecol\lacZ<up>gypsy.PP</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 658
ID|FBtr0000991
SYM|Ecol\lacZ<up>gypsy.PP</up>RA
SYN|lacZ<up>gypsy.PP</up>RA
ASAL|<fbsym>FBal0041516==Ecol\lacZ<up>gypsy.PP</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0000992
ASTP|<fbsym>FBtp0004304==P{gypCaSpeR}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0076432
|Pelisson et al.
|1994
RNAT|mRNA
BODP|<fbsym>FBgn0014447==Ecol\lacZ</fbsym> expression is observed in follicle cells of females permissive
| for gypsy activity.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> O,A <a> follicle cell <p>
}

REF
{
REFM|FBrf0076432
|Pelisson et al.
|1994
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0000992	SYM 1 gypsy\env-RA	TRL 1 2.072	ASM 1 in situ	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 2	DT 1 5 Sep 2001	RESZ 791
ID|FBtr0000992
SYM|gypsy\env-RA
SYN|gypsy\env<up>+</up>R2.1
ASAL|<fbsym>FBal0105307==gypsy\env<up>+</up></fbsym>
DT|5 Sep 2001
|10 Mar 1998
ID2|FBtr0000993
ASGN|<fbsym>FBgn0014964==gypsy\env</fbsym>
ASPP|<fbsym>FBpp0001768==gypsy\env-P1</fbsym>

REFDSR
{
RDID|FBrf0076432
|Pelisson et al.
|1994
RNAT|mRNA
TRL|2.1 (northern blot)
BODP|Transcripts are detected in the follicle cells of females of strains
| permissive for gypsy activity. Expression is not uniform within follicle
| cells but appears to be concentrated near the oocyte.
ASM|in situ
CVBODP|in situ
|<t> O,A <a> follicle cell <p>
CC|A subgenomic RNA.
}

REFDSR
{
RDID|FBrf0076478
|Avedisov and Ilyin
|1994
RNAT|mRNA
TRL|2.072 (nb, sa)
}

REF
{
REFM|FBrf0076432
|Pelisson et al.
|1994
REFM|FBrf0076478
|Avedisov and Ilyin
|1994
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001032	SYM 1 Btau\MAPT<up>ap.C.T:Ecol\lacZ</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 16 Aug 2000	RESZ 1360
ID|FBtr0001032
SYM|Btau\MAPT<up>ap.C.T:Ecol\lacZ</up>RA
SYN|btau<up>ap.C.T:lacZ</up>RA
ASAL|<fbsym>FBal0044381==Ecol\lacZ<up>ap.C.T:Btau\MAPT</up></fbsym>
DT|16 Aug 2000
|10 Mar 1998
ID2|FBtr0001033
ASTP|<fbsym>FBtp0004965==P{apC-tau-lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0078940
|Lundgren et al.
|1995
RNAT|mRNA
BODP|Analysis of <fbsym>Btau\MAPT[ap.C.T:Ecol\lacZ]</fbsym> expression suggests that <fbsym>FBgn0000099==ap</fbsym>
|-expressing cells are interneurons that start to elongate axons soon after
| they begin expressing <fbsym>FBgn0000099==ap</fbsym> protein.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> ventral nerve cord | restricted <p>
|<t> E <a> interneuron <p>
|<t> L <a> dorsal mesothoracic disc <p>
ASCRGN|<fbsym>FBgn0000099==ap</fbsym>
}

REFDSR
{
RDID|FBrf0105986
|Thor et al.
|1999
RNAT|mRNA
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> interneuron | subset <p>
ASCRGN|<fbsym>FBgn0000099==ap</fbsym>
CC|<fbsym>FBgn0002023==Lim3</fbsym> is not co-expressed with <fbsym>FBgn0003896==tup</fbsym> or <fbsym>FBgn0000099==ap</fbsym> in interneurons.
}

REF
{
REFM|FBrf0078940
|Lundgren et al.
|1995
REFM|FBrf0105986
|Thor et al.
|1999
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001035	SYM 1 so<up>+</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 384
ID|FBtr0001035
SYM|so<up>+</up>RA
ASAL|<fbsym>FBal0071116==so<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0001036
ASGN|<fbsym>FBgn0003460==so</fbsym>
ASPP|<fbsym>FBpp0001280==so-P1</fbsym>

REFDSR
{
RDID|FBrf0079386
|Serikaku and O'Tousa
|1994
RNAT|mRNA
EXNSQ|1b,2-7
CC|Minor <fbsym>FBgn0003460==so</fbsym> transcript.
}

REF
{
REFM|FBrf0079386
|Serikaku and O'Tousa
|1994
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001037	SYM 1 Ecol\lacZ<up>ct.wHZ</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 674
ID|FBtr0001037
SYM|Ecol\lacZ<up>ct.wHZ</up>RA
SYN|lacZ<up>ct.wHZ</up>RA
ASAL|<fbsym>FBal0041036==Ecol\lacZ<up>ct.wHZ</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0001038
ASTP|<fbsym>FBtp0000951==P{ctwHZ}</fbsym>
|<fbsym>FBmc0001004==pP{ctwHZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0079512
|Thomas et al.
|1995
RNAT|mRNA
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar <a> dorsal mesothoracic disc | restricted <p>
|<t> L | third instar <a> marginal cell <p>
ASCRGN|<fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0079512
|Thomas et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001046	SYM 1 Ecol\lacZ<up>vvl.RX</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 30 Jun 1999	RESZ 977
ID|FBtr0001046
SYM|Ecol\lacZ<up>vvl.RX</up>RA
SYN|lacZ<up>RX-dfr</up>RA
ASAL|<fbsym>FBal0047925==Ecol\lacZ<up>vvl.RX</up></fbsym>
DT|30 Jun 1999
|10 Mar 1998
ID2|FBtr0001047
ASTP|<fbsym>FBtp0005727==P{RX-dfr-lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0079852
|Anderson et al.
|1995
RNAT|mRNA
BODP|The <fbsym>FBgn0014447==Ecol\lacZ</fbsym> reporter gene is strongly expressed in the developing
| tracheal tree and in the lateral oenocyte clusters but not in the stage
| 10/11 mesectoderm or the epidermis where <fbsym>FBgn0003995==vvl</fbsym> is normally strongly
| expressed. It is also expressed in the middle (MGM) and anterior (MGA)
| pairs of midline glia.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E | stage 13-16 <a> abdominal 1..7 larval oenocyte group <p>
|<t> E | stage >=10 <a> midline glial cell <p>
}

REF
{
REFM|FBrf0079852
|Anderson et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001053	SYM 1 oaf<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 1783
ID|FBtr0001053
SYM|oaf<up>+</up>R
ASAL|<fbsym>FBal0070839==oaf<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0001054
ASGN|<fbsym>FBgn0011818==oaf</fbsym>

REFDSR
{
RDID|FBrf0079893
|Bergstrom et al.
|1995
RNAT|mRNA
BODP|In early embryos, <fbsym>FBgn0011818==oaf</fbsym> transcripts are distributed uniformly. During
| cellularization, gastrulation, and germ band extension, they are
| distributed throughout the cellular portion of the embryo. At maximum germ
| band extension, areas of higherlocalized accumulation appear in most
| segments in clusters of cells (or in single cells in the abdominal
| segments). During germ band retraction, the localized expression
| disappears. The level of ubiquitous transcripts declines and then remains
| constant until the end of embryonic development. Localized expression
| resumes in stage 15 with expression in sets of segmentally repeated cells
| along the ventral midline and in the peripheral part of the nerve cord, as
| well as in the brain and gonad. In third instar larvae, strong expression
| is seen in male gonads with the highest levels in spermatocytes in the
| terminal end of the gonad. In ovaries, expression is observed in nurse
| cells at all stages and in the developing oocyte.
ASM|in situ
CVBODP|in situ
|<t> E <a>  <p> ubiquitous
|<t> E | stage 11 <a> germ band | restricted <p>
|<t> E | stage >15 <a> ventral nerve cord | segmentally repeated <p>
|<t> E | stage >15 <a> ventral midline | segmentally repeated <p>
|<t> E | stage >15 <a> embryonic brain <p>
|<t> E | stage >15 <a> gonad <p>
|<t> L,S | third instar <a> testis <p>
|<t> L,S | third instar <a> spermatocyte <p>
|<t> O,A | female <a> ovary <p>
|<t> O,A <a> nurse cell <p>
|<t> O,A <a> oocyte <p>
}

REF
{
REFM|FBrf0079893
|Bergstrom et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001080	SYM 1 Ecol\lacZ<up>ct.F</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 957
ID|FBtr0001080
SYM|Ecol\lacZ<up>ct.F</up>RA
SYN|lacZ<up>ct.F</up>RA
ASAL|<fbsym>FBal0047637==Ecol\lacZ<up>ct.F</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0001081
ASTP|<fbsym>FBtp0005534==P{cutF-hsp70-lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0080124
|Jack and DeLotto
|1995
RNAT|mRNA
BODP|A 3.3 kb EcoRI fragment of the <fbsym>FBgn0004198==ct</fbsym> regulatory region fused to a minimal
| Hsp70 promoter drives <fbsym>FBgn0014447==Ecol\lacZ</fbsym> expression in the embryonic central
| nervous system, as well as in the ventral ganglion and optic lobe of the larva.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> central nervous system <p>
|<t> L | third instar <a> larval ventral ganglion <p>
|<t> L | third instar <a> larval optic lobe <p>
ASCRGN|<fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0080124
|Jack and DeLotto
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001081	SYM 1 Ecol\lacZ<up>ct.E</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 1358
ID|FBtr0001081
SYM|Ecol\lacZ<up>ct.E</up>RA
SYN|lacZ<up>ct.E</up>RA
ASAL|<fbsym>FBal0047636==Ecol\lacZ<up>ct.E</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0001082
ASTP|<fbsym>FBtp0005533==P{cutE-hsp70-lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0080124
|Jack and DeLotto
|1995
RNAT|mRNA
BODP|A 6.5kb EcoRI fragment of the <fbsym>FBgn0004198==ct</fbsym> regulatory region fused to a minimal
| Hsp70 promoter drives expression of <fbsym>FBgn0014447==Ecol\lacZ</fbsym> in embryonic, larval, and
| adult tissues. In the embryo, <fbsym>FBgn0014447==Ecol\lacZ</fbsym> expression is seen in tracheal
| histoblasts, anterior spiracles, and weakly in the Malpighian tubules. In
| the larva, the ventral ganglion expresses <fbsym>FBgn0014447==Ecol\lacZ</fbsym>, while in the adult,
| <fbsym>FBgn0014447==Ecol\lacZ</fbsym> is found in simple external sensory organs (with the exception
| of the chemo- and mechanoreceptors on the wing margin).
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E | stage 12 <a> histoblast <p>
|<t> E <a> embryonic/larval anterior spiracle <p>
|<t> L | third instar <a> larval ventral ganglion <p>
|<t> A <a> external sensory organ <p>
ASCRGN|<fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0080124
|Jack and DeLotto
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001082	SYM 1 Ecol\lacZ<up>ct.D</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 1683
ID|FBtr0001082
SYM|Ecol\lacZ<up>ct.D</up>RA
SYN|lacZ<up>ct.D</up>RA
ASAL|<fbsym>FBal0047635==Ecol\lacZ<up>ct.D</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0001083
ASTP|<fbsym>FBtp0005532==P{cutD-hsp70-lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0080124
|Jack and DeLotto
|1995
RNAT|mRNA
BODP|A 3.8kb HindIII fragment of the <fbsym>FBgn0004198==ct</fbsym> regulatory region fused to a minimal
| Hsp70 promoter drives expression of <fbsym>FBgn0014447==Ecol\lacZ</fbsym> in embryonic and larval
| tissues. In the embryonic central nervous system (CNS), <fbsym>FBgn0014447==Ecol\lacZ</fbsym>
| expression is visible in 4 cells per segment. In the embryonic peripheral
| nervous system (PNS), <fbsym>FBgn0014447==Ecol\lacZ</fbsym> is expressed in the antenno-maxillary
| organs, the hypophysis, and the epiphysis. The ventral end of fascicles
| which carry axons from the PNS into the ganglia of the CNS express
| <fbsym>FBgn0014447==Ecol\lacZ</fbsym> in both embryos and late third instar larvae. A subset of cells
| in the internal portion of the posterior spiracles of the embryo express
| <fbsym>FBgn0014447==Ecol\lacZ</fbsym>. <fbsym>FBgn0014447==Ecol\lacZ</fbsym> staining in the Malpighian tubules is weak.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> larval labral sense organ <p>
|<t> E <a> hypophysis <p>
|<t> E-L <a> fascicle <p>
|<t> E <a> embryonic central nervous system | restricted <p>
|<t> E <a> Malpighian tubule <p>
|<t> E <a> antenno-maxillary complex <p>
ASCRGN|<fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0080124
|Jack and DeLotto
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001083	SYM 1 Ecol\lacZ<up>ct.C</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 976
ID|FBtr0001083
SYM|Ecol\lacZ<up>ct.C</up>RA
SYN|lacZ<up>ct.C</up>RA
ASAL|<fbsym>FBal0047634==Ecol\lacZ<up>ct.C</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0001084
ASTP|<fbsym>FBtp0005531==P{cutC-hsp70-lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0080124
|Jack and DeLotto
|1995
RNAT|mRNA
BODP|A 5.4kb EcoRI fragment of the <fbsym>FBgn0004198==ct</fbsym> regulatory region fused to a minimal
| Hsp70 promoter drives <fbsym>FBgn0014447==Ecol\lacZ</fbsym> expression in the inner cells of the
| posterior spiracles, the antenno-maxillary organs, the hypophysis, and the Malpighiantubules.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> antenno-maxillary complex <p>
|<t> E <a> hypophysis <p>
|<t> E <a> posterior spiracle primordium <p>
|<t> E <a> Malpighian tubule <p>
ASCRGN|<fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0080124
|Jack and DeLotto
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001084	SYM 1 Ecol\lacZ<up>ct.B</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 1006
ID|FBtr0001084
SYM|Ecol\lacZ<up>ct.B</up>RA
SYN|lacZ<up>ct.B</up>RA
ASAL|<fbsym>FBal0047633==Ecol\lacZ<up>ct.B</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0001085
ASTP|<fbsym>FBtp0005530==P{cutB-hsp70-lacZ}</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0080124
|Jack and DeLotto
|1995
RNAT|mRNA
BODP|A 3.3kb EcoRI fragment of the <fbsym>FBgn0004198==ct</fbsym> regulatory region fused to a minimal
| Hsp70 promoter drives <fbsym>FBgn0014447==Ecol\lacZ</fbsym> expression in the Malpighian tubules,
| ephyphisis and hypophysis of the embryo, and in the optic lobes and the
| connectives between the optic lobes and central ganglion of the larva.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> larval labral sense organ <p>
|<t> E <a> hypophysis <p>
|<t> L | third instar <a> larval brain | restricted <p>
ASCRGN|<fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0080124
|Jack and DeLotto
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001085	SYM 1 Ecol\lacZ<up>ct.A</up>RA	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 324
ID|FBtr0001085
SYM|Ecol\lacZ<up>ct.A</up>RA
SYN|lacZ<up>ct.A</up>RA
ASAL|<fbsym>FBal0047632==Ecol\lacZ<up>ct.A</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0001086
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0080124
|Jack and DeLotto
|1995
RNAT|mRNA
}

REF
{
REFM|FBrf0080124
|Jack and DeLotto
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001111	SYM 1 InR<up>+</up>R	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 327
ID|FBtr0001111
SYM|InR<up>+</up>R
ASAL|<fbsym>FBal0067936==InR<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0001112
ASGN|<fbsym>FBgn0013984==InR</fbsym>
ASPP|<fbsym>FBpp0000690==InR<up>+</up>P2148</fbsym>

REFDSR
{
RDID|FBrf0080360
|Ruan et al.
|1995
RNAT|mRNA
EXNSQ|1-10
}

REF
{
REFM|FBrf0080360
|Ruan et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001129	SYM 1 mnb<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 565
ID|FBtr0001129
SYM|mnb<up>+</up>R
ASAL|<fbsym>FBal0070653==mnb<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0001130
ASGN|<fbsym>FBgn0002777==mnb</fbsym>

REFDSR
{
RDID|FBrf0080444
|Tejedor et al.
|1995
RNAT|mRNA
BODP|<fbsym>FBgn0002777==mnb</fbsym> transcripts are detected in the ventral nerved cord and in the
| supraoesophageal ganglion by in situ hybridization but not in neuroblasts
| or in the PNS.
ASM|in situ
CVBODP|in situ
|<t> E <a> ventral nerve cord <p>
|<t> E <a> supraoesophageal ganglion <p>
}

REF
{
REFM|FBrf0080444
|Tejedor et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001139	SYM 1 shn<up>+</up>RC	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 524
ID|FBtr0001139
SYM|shn<up>+</up>RC
ASAL|<fbsym>FBal0071046==shn<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0001140
ASGN|<fbsym>FBgn0003396==shn</fbsym>

REFDSR
{
RDID|FBrf0081322
|Arora et al.
|1995
RNAT|mRNA
EXNSQ|1L
CC|The C class of <fbsym>FBgn0003396==shn</fbsym> message contains an extended exon 1 and no other
| sequences. Evidence for its existence comes from a cDNA and the
| hybridization of this cDNA to embryos. It does not contain any coding sequences.
}

REF
{
REFM|FBrf0081322
|Arora et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001209	SYM 1 Btau\MAPT<up>P\T.T:Ecol\lacZ</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 1367
ID|FBtr0001209
SYM|Btau\MAPT<up>P\T.T:Ecol\lacZ</up>RA
SYN|btau<up>P\T.T:lacZ</up>RA
|tau<up>P\T.T:lacZ</up>RA
ASAL|<fbsym>FBal0044377==Ecol\lacZ<up>P\T.T:Btau\MAPT</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0001210
ASTP|<fbsym>FBtp0001352==P{etau-lacZ}</fbsym>
|<fbsym>FBms0003726==P\T::btau::lacZ(P5',Bg2)</fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0081545
|Callahan et al.
|1995
RNAT|mRNA
BODP|Enhancer trap expression is restricted to a cluster of about 20 interneurons
| per hemisegment. Expression commences postmitotically in the neurons as
| they begin elongating axons and continues throughout embryogenesis. Most or
| all extend their axons acrossthe midline along the anterior commissure.
| Upon reaching the contralateral longitudinal connective, the growth cones
| turn anteriorly and follow one of two discrete pathways at the medial edge
| of the connective. When they reach the adjacent anterior segment, they
| fasciculate with their homologues, forming two continuous axon fascicles in
| each connective.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> interneuron <p>
|<t> E <a> anterior commissure <p>
|<t> E <a> longitudinal connectives <p>
ASCRGN|<fbsym>FBgn0015380==drl</fbsym>
}

REF
{
REFM|FBrf0081545
|Callahan et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001220	SYM 1 belt<up>+</up>RA	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 431
ID|FBtr0001220
SYM|belt<up>+</up>RA
ASAL|<fbsym>FBal0068684==belt<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0001221
ASGN|<fbsym>FBgn0005635==belt</fbsym>

REFDSR
{
RDID|FBrf0081987
|Feinstein et al.
|1995
RNAT|mRNA
BODP|<fbsym>FBgn0005635==belt</fbsym> was shown to be induced by ubiquitous <fbsym>FBgn0003944==Ubx</fbsym> expression during embryogenesis.
ASM|in situ
}

REF
{
REFM|FBrf0081987
|Feinstein et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001269	SYM 1 CycE<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 3	DT 1 23 Dec 2000	RESZ 917
ID|FBtr0001269
SYM|CycE<up>+</up>R
SYN|CytE<up>+</up>R
ASAL|<fbsym>FBal0066527==CycE<up>+</up></fbsym>
DT|23 Dec 2000
|10 Mar 1998
ID2|FBtr0001270
|FBtr0001372
|FBtr0001373
ASGN|<fbsym>FBgn0010382==CycE</fbsym>

REFDSR
{
RDID|FBrf0082560
|Sauer et al.
|1995
RNAT|mRNA
}

REFDSR
{
RDID|FBrf0084309
|Richardson et al.
|1995
RNAT|mRNA
}

REFDSR
{
RDID|FBrf0102951
|Kerber et al.
|1998
RNAT|mRNA
BODP|During Malpighian tubule development, <fbsym>FBgn0010382==CycE</fbsym> is expressed asymmetrically in
| everting tubules, and subsequently in the distal proliferation zone. With
| the onset of endomitotic cycles, <fbsym>FBgn0010382==CycE</fbsym> is also expressed from proximal to
| distal in the tubules.
ASM|in situ
CVBODP|in situ
|<t> E | stage >=10 <a> Malpighian tubule | restricted <p>
}

REF
{
REFM|FBrf0082560
|Sauer et al.
|1995
REFM|FBrf0084309
|Richardson et al.
|1995
REFM|FBrf0102951
|Kerber et al.
|1998
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001353	SYM 1 fax<up>+</up>RB	TRL 1 -	ASM 1 -	CDNA 1 -	ASPP 1 +	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 574
ID|FBtr0001353
SYM|fax<up>+</up>RB
ASAL|<fbsym>FBal0068930==fax<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0001354
ASGN|<fbsym>FBgn0014163==fax</fbsym>
ASPP|<fbsym>FBpp0001810==fax<up>+</up>P415</fbsym>

REFDSR
{
RDID|FBrf0084025
|Hill et al.
|1995
RNAT|mRNA
EXNSQ|1,2b,3,4
CC|Evidence for this alternate form of <fbsym>FBgn0014163==fax</fbsym> RNA that uses an alternate splice
| acceptor for intron 2 comes from RT-PCR results. The relative abundance or
| importance of the two transcripts has not been determined.
}

REF
{
REFM|FBrf0084025
|Hill et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001355	SYM 1 Ecol\lacZ<up>gcm-P</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 14 May 1999	RESZ 2134
ID|FBtr0001355
SYM|Ecol\lacZ<up>gcm-P</up>RA
SYN|lacZ<up>gcm-P</up>RA
ASAL|<fbsym>FBal0047719==Ecol\lacZ<up>gcm-P</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0001356
ASTI|<fbsym>FBti0002949==P{PZ}gcm<up>P</up></fbsym>
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0084044
|Hosoya et al.
|1995
RNAT|mRNA
BODP|lacZ expression visible in whole cell body. No expression observed in
| midline glia.
ASM|transcript distribution deduced from reporter protein
RNAT|mRNA
BODP|<fbsym>FBgn0014179==gcm</fbsym> transcripts are expressed in glial precursors and immature glial cells
| during a short period of gliogenesis. Expression is first detected in early
| stage 11 in the longitudinal glioblast. By mid stage 11, 2-3 other cells
| per hemisegment express <fbsym>FBgn0014179==gcm</fbsym>. Two of these have been identified as NB6-4
| and the medial-most cell body glial cell (VUM support cell). By early stage
| 12, expression is detected in several other cells which are also developing
| glial cells. Expression fades during stage 12 and is hardly detectable in
| stage 13. Enhancer trap expression was used to trace the <fbsym>FBgn0014179==gcm</fbsym>-expressing
| cells to later developmental stages. It was found that <fbsym>FBgn0014179==gcm</fbsym> is expressed
| in all glial precursors and immature glial cells except those derived from
| the mesectoderm. Outside of the CNS, <fbsym>FBgn0014179==gcm</fbsym> is expressed in the most
| anterior region of the presumptive mesoderm beginning at the cellular
| blastoderm stage, in the brain neurogenic region, and in the PNS neurogenic region.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E | stage >=11 <a> interface glial cell | precursor <p>
|<t> E | stage >=11 <a> neuroblast NB6-4 <p>
|<t> E | stage >=11 <a> medial-most cell body glial cell <p>
|<t> E | stage >=11 <a> glial cell <p><t> E <a> peripheral nervous system <p>
|<t> E <a> embryonic brain <p>
|<t> E | cellular blastoderm <a>  <p>
ASCRGN|<fbsym>FBgn0014179==gcm</fbsym>
}

REF
{
REFM|FBrf0084044
|Hosoya et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001362	SYM 1 sr<up>+</up>R	TRL 1 -	ASM 1 in situ	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 1	DT 1 7 Apr 1998	RESZ 719
ID|FBtr0001362
SYM|sr<up>+</up>R
ASAL|<fbsym>FBal0071143==sr<up>+</up></fbsym>
DT|7 Apr 1998
|10 Mar 1998
ID2|FBtr0001363
ASGN|<fbsym>FBgn0003499==sr</fbsym>

REFDSR
{
RDID|FBrf0084118
|Lee et al.
|1995
RNAT|mRNA
BODP|<fbsym>FBgn0003499==sr</fbsym> transcripts are expressed from embryonic stage 14 in segment border
| cells, which serve as attachment sites for developing myotubes. They are
| not found in developing muscle.
ASM|in situ
CVBODP|<t> E | stage >=14 <a> muscle attachment site <p>
CC|It is not clear to which transcript the cDNA corresponds and the predicted
| protein sequence from the cDNA is common to both forms of <fbsym>FBgn0003499==sr</fbsym> protein.
}

REF
{
REFM|FBrf0084118
|Lee et al.
|1995
}

}

# EOR

TRR
{

RETE|ID 1 FBtr0001404	SYM 1 Ecol\lacZ<up>arm.PV</up>RA	TRL 1 -	ASM 1 transcript distribution deduced from reporter protein	CDNA 1 -	ASPP 1 -	DBA 1 -	REF 1 2	DT 1 14 May 1999	RESZ 1175
ID|FBtr0001404
SYM|Ecol\lacZ<up>arm.PV</up>RA
SYN|lacZ<up>arm.PV</up>RA
ASAL|<fbsym>FBal0040819==Ecol\lacZ<up>arm.PV</up></fbsym>
DT|14 May 1999
|10 Mar 1998
ID2|FBtr0001405
ASTP|<fbsym>FBtp0001247==P{arm-lacZ.V}</fbsym>
|<fbsym>FBmc0001237==pP{arm-lacZ.V}</fbsym>
|<fbsym>FBtp0012986==P{HF11}</fbsym>
ASGN|<fbsym>FBgn0014445==Scer\GAL4</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0074716
|Vincent et al.
|1994
RNAT|mRNA
BODP|In embryos, expression first detectable during early gastrulation; high by
| late stage 9.  In larvae, no detectable expression in the midgut;
| expression in almost all other tissues, including discs.
ASM|transcript distribution deduced from reporter protein
CVBODP|transcript distribution deduced from reporter protein
|<t> E stage >=6 <a>  <p> ubiquitous
|<t> L <a>  <p> ubiquitous
|<t> P <a>