dorsal mesothoracic disc | restricted
}
REF
{
REFM|FBrf0077493
|Murakami et al.
|1994
REFM|FBrf0084211
|Murakami et al.
|1995
REFM|FBrf0111436
|Moreno and Morata
|1999
REFM|FBrf0151948
|Johansen et al.
|2003
REFM|FBrf0178997
|Copf et al.
|2003
}
ALESR
{
ASYM|FBal0057714==bynapro
REFDSR
{
RDID|FBrf0084211
|Murakami et al.
|1995
PHP|Degeneration of the proctodeum during shortening of the germ band stage.
PHM|proctodeum
}
REF
{
REFM|FBrf0084211
|Murakami et al.
|1995
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004135 ICL 1 P SYM 1 P{hsneo}ifcdes ASTR 1 - CLOC 1 26B2 REF 1 2 DT 1 8 Oct 1997 RESZ 529
ID|FBti0004135
SYM|P{hsneo}ifcdes
ASTP|FBtp0000078==P{hsneo}
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|FBgn0001941==ifc
ARGS|FBgn0001941
REFDSR
{
RDID|FBrf0091054
|Endo et al.
|1996
SYN|P{hsneo}ifcdes
ASAL|FBal0057253==ifcdes
CLOC|26B2
|Insertion site
LOCB|Proximity to gene: FBgn0001941==ifc
PHC|male sterile | recessive
|semi-lethal | embryonic stage | recessive
}
REF
{
REFM|FBrf0091054
|Endo et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0057253==ifcdes
REFDSR
{
RDID|FBrf0091054
|Endo et al.
|1996
PHP|20-50% of homozygotes die during the embryonic stages.
|Female fertility is unaffected.
|Mutants testes are smaller than wild type and do not contain elongated
|spermatids. Primary spermatocytes enter the growth phase, giving rise
|to morphologically mature primary spermatocytes with normal large nuclei,
|prominent nucleoli and decondensed chromosomes. They then degenerate
|without initiating the meiotic chromosome condensation that normally
|... (see FBal0057253==ifcdes report)
PHM|testis
|spermatid
}
REF
{
REFM|FBrf0091054
|Endo et al.
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004141 ICL 1 P SYM 1 P{lArB}emcP ASTR 1 - CLOC 1 61C9 REF 1 2 DT 1 8 Oct 1997 RESZ 437
ID|FBti0004141
SYM|P{lArB}emcP
ASTP|FBtp0000160==P{lArB}
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|FBgn0000575==emc
REFDSR
{
RDID|FBrf0090681
|Mackay and Fry
|1996
SYN|P{lArB}emcP
ASAL|FBal0057500==emcP
CLOC|61C9
|Insertion site
LOCB|Proximity to gene: FBgn0000575==emc
}
REF
{
REFM|FBrf0090681
|Mackay and Fry
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0004148 ICL 1 P SYM 1 P{lwB}aflts ASTR 1 - CLOC 1 - REF 1 2 DT 1 8 Oct 1997 RESZ 442
ID|FBti0004148
SYM|P{lwB}aflts
ASTP|FBtp0000157==P{lwB}
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|FBgn0019909==afl
REFDSR
{
RDID|FBrf0091451
|Sur et al.
|1996
SYN|P{lwB}aflts
ASAL|FBal0057939==aflts
LOCB|Proximity to gene: FBgn0019909==afl
PHC|lethal | recessive | conditional ts
}
REF
{
REFM|FBrf0091451
|Sur et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0057939==aflts
REFDSR
{
RDID|FBrf0091451
|Sur et al.
|1996
PHP|Most homozygotes die as embryos or larvae, viability of homozygous
|females is always lower then that of homozygous males. Rare escapers
|are semi-sterile but morphologically normal.
}
REF
{
REFM|FBrf0091451
|Sur et al.
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004228 ICL 1 P SYM 1 P{lacW}nejP ASTR 1 - CLOC 1 8F7--9 REF 1 4 DT 1 8 Oct 1997 RESZ 901
ID|FBti0004228
SYM|P{lacW}nejP
SYN|pw+nej
ASTP|FBtp0000204==P{lacW}
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|FBgn0015624==nej
SK|FBst0003728
|w[*] P{w[+mC]=lacW}nej[P]/FM7c
|Total=1
REFDSR
{
RDID|FBrf0093058
|Akimaru et al.
|1997
SYN|P{lacW}nejP
ASAL|FBal0059991==nejP
CLOC|8F7--9
|Insertion site
LOCB|Proximity to gene: FBgn0015624==nej
}
REFDSR
{
RDID|FBrf0138518
|Kiger et al.
|2001
SYN|pw+nej
}
REFDSR
{
RDID|FBrf0180303
|Kumar et al.
|2004
PHC|(with nej3) lethal
|(with nejQ7) lethal
|(with nejS103) lethal
|(with nejS342) lethal
|(with nejTA57) lethal
}
REF
{
REFM|FBrf0093058
|Akimaru et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0138518
|Kiger et al.
|2001
REFM|FBrf0180303
|Kumar et al.
|2004
}
ALESR
{
ASYM|FBal0059991==nejP
REFDSR
{
RDID|FBrf0180303
|Kumar et al.
|2004
PHP|The FBal0059991==nejP/FBal0094382==nejTC41 and
| FBal0059991==nejP/FBal0175574==nej131 combinations give
|viable adults with moderately rough eyes. The ommatidia have variable
|numbers of photoreceptor cells in
| FBal0059991==nejP/FBal0175574==nej131 adults.
PHM|(with nejTC41) eye
|(with nejTC41) ommatidium
|(with nej131) eye
|(with nej131) ommatidium
|(with nej131) photoreceptor cell
}
REF
{
REFM|FBrf0180303
|Kumar et al.
|2004
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004290 ICL 1 P SYM 1 P{lacW}III-P ASTR 1 - CLOC 1 - REF 1 2 DT 1 8 Oct 1997 RESZ 438
ID|FBti0004290
SYM|P{lacW}III-P
ASTP|FBtp0000204==P{lacW}
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|FBgn0003996==w
|FBgn0014447==Ecol\lacZ
REFDSR
{
RDID|FBrf0084765
|Bhojwani et al.
|1995
SYN|P{lacW}III-P
ASAL|FBal0061069==Ecol\lacZwg-III-P
|FBal0060826==wwg-III-P
}
REF
{
REFM|FBrf0084765
|Bhojwani et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0004773 ICL 1 P SYM 1 P{UAS-hh.A}III ASTR 1 - CLOC 1 61-100 REF 1 2 DT 1 10 May 1999 RESZ 350
ID|FBti0004773
SYM|P{UAS-hh.A}III
SYN|P{UAS-hh.A1}III
|P{UAShh.1}III
ASTP|FBtp0001373==P{UAS-hh.A}
DT|10 May 1999
|29 Dec 1997
ICL|P
REFDSR
{
RDID|FBrf0098056
|Frasch
|1997.7.23
SYN|P{UAShh.1}III
GLOC|61-100
|Insertion site
LOCB|Mapped to chromosome #3
}
REF
{
REFM|FBrf0098056
|Frasch
|1997.7.23
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0004774 ICL 1 P SYM 1 P{GawB}rhl ASTR 1 - CLOC 1 62A2 REF 1 3 DT 1 29 Dec 1997 RESZ 604
ID|FBti0004774
SYM|P{GawB}rhl
ASTP|FBtp0000352==P{GawB}
DT|29 Dec 1997
|29 Dec 1997
ICL|P
ASGN|FBgn0004635==rho
|FBgn0014445==Scer\GAL4
REFDSR
{
RDID|FBrf0086318
|Axelrod et al.
|1996
ASAL|FBal0083445==Scer\GAL4rho-rhl
}
REFDSR
{
RDID|FBrf0099060
|Noll
|1997.12.3
CLOC|62A2
|Insertion site
LOCB|Proximity to gene: FBgn0004635==rho
CH|binary enhancer trap | FBgn0004635==rho
PHC|viable
}
REF
{
REFM|FBrf0086318
|Axelrod et al.
|1996
REFM|FBrf0099060
|Noll
|1997.12.3
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0005135 ICL 1 P SYM 1 P{hsneo}rtP ASTR 1 - CLOC 1 68C1-68C8 REF 1 6 DT 1 31 Jan 1998 RESZ 1152
ID|FBti0005135
SYM|P{hsneo}rtP
SYN|fs(3)neo1
ASTP|FBtp0000078==P{hsneo}
DT|31 Jan 1998
|3 Jan 1998
ICL|P
ID2|FBti0000118
ASGN|FBgn0003292==rt
SK|FBst0010060
|mwh[1] P{hsneo}rt[P] red[1] e[1]/TM3, Sb[1] Ser[1]
|Total=1
REFDSR
{
RDID|FBrf0049003
|Cooley et al.
|1988
SYN|P{hsneo}rtP
ASAL|FBal0014813==rtP
CLOC|68C1-68C8
|Insertion site
LOCB|in situ
}
REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
CLOC|68C1-68C8
|Insertion site
LOCB|in situ
DBAF|AQ025579.1 Dual_flanking_Example.JPG
}
REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
PHC|female sterile | recessive
}
REFDSR
{
RDID|FBrf0184339
|FlyBase
|2005
CC|Location 3L:622835-622836 confirmed by FlyBase alignment of dbGSS accession
| AQ025579 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b.
| Insertion orientation confirmed.
}
REF
{
REFM|FBrf0049003
|Cooley et al.
|1988
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
REFM|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111489
|Spradling et al.
|1999
REFM|FBrf0184339
|FlyBase
|2005
}
ALESR
{
ASYM|FBal0014813==rtP
REFDSR
{
RDID|FBrf0049003
|Cooley et al.
|1988
PHP|Homozygous males and females have reduced fertility and show
|abdominal rotation.
PHM|adult abdomen
}
REFDSR
{
RDID|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
PHP|The bodies of first instar larvae are rotated around the long axis,
|forcing the animals to move in a clockwise circle as they crawl. The
|larval cuticle presents a perfect segmental alignment of landmarks
|but the adult abdominal cuticle segments appear staggered relative
|to each other.
PHM|adult cuticle
}
REF
{
REFM|FBrf0049003
|Cooley et al.
|1988
REFM|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0005676 ICL 1 P SYM 1 P{lArB}DlEW ASTR 1 - CLOC 1 92A1--2 REF 1 2 DT 1 3 Jan 1998 RESZ 438
ID|FBti0005676
SYM|P{lArB}DlEW
ASTP|FBtp0000160==P{lArB}
DT|3 Jan 1998
|3 Jan 1998
ICL|P
ASGN|FBgn0000463==Dl
REFDSR
{
RDID|FBrf0098270
|Huppert et al.
|1997
SYN|P{lArB}DlEW
ASAL|FBal0038738==DlEW
CLOC|92A1--2
|Insertion site
LOCB|Proximity to gene: FBgn0000463==Dl
}
REF
{
REFM|FBrf0098270
|Huppert et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0038738==DlEW
REFDSR
{
RDID|FBrf0098270
|Huppert et al.
|1997
PHP|Wing veins are extremely thickened - all cells within the provein adopt
|the vein cell fate.
PHM|wing vein
|eye
}
REF
{
REFM|FBrf0098270
|Huppert et al.
|1997
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0007116 ICL 1 P SYM 1 P{lacW}LamP ASTR 1 - CLOC 1 25E6 REF 1 3 DT 1 3 Jan 1998 RESZ 641
ID|FBti0007116
SYM|P{lacW}LamP
ASTP|FBtp0000204==P{lacW}
DT|3 Jan 1998
|3 Jan 1998
ICL|P
ASGN|FBgn0002525==Lam
REFDSR
{
RDID|FBrf0083257
|Lenz et al.
|1995
PHC|sterile
|semi-lethal
}
REFDSR
{
RDID|FBrf0093570
|Lenz-Bohme et al.
|1997
SYN|P{lacW}LamP
ASAL|FBal0065070==LamP
CLOC|25E6
|Insertion site
LOCB|Proximity to gene: FBgn0002525==Lam
PHC|male sterile | recessive
|female sterile | recessive
|lethal | recessive | partially
}
REF
{
REFM|FBrf0083257
|Lenz et al.
|1995
REFM|FBrf0093570
|Lenz-Bohme et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0065070==LamP
REFDSR
{
RDID|FBrf0083257
|Lenz et al.
|1995
PHP|The few surviving adults show reduced viability combined with locomotion
|ataxy. They cannot fly and walking is difficult. Males and females
|are sterile.
}
REFDSR
{
RDID|FBrf0093570
|Lenz-Bohme et al.
|1997
PHP|Homozygotes have a prolonged developmental time course, with a delay
|of up to 3 days at 24oC. Only 5-10% of homozygotes survive until
|adulthood, with survival rate being inversely correlated with population
|density. There are three major periods of homozygous lethality; including
|the embryonic stages (20-30% lethality), the pupal stages (50-60% lethality),
|and the eclosion of the adult fly (5-10% lethality). Adults die within
|two weeks of eclosion.
|... (see FBal0065070==LamP report)
PHM|ovary
|ovariole
|oocyte
|spermatozoon
|nuclear pore
|annulate lamellae
|nuclear membrane
}
REF
{
REFM|FBrf0083257
|Lenz et al.
|1995
REFM|FBrf0093570
|Lenz-Bohme et al.
|1997
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0009066 ICL 1 P SYM 1 P{lacZ}exbrl ASTR 1 - CLOC 1 21C2 REF 1 2 DT 1 7 May 1998 RESZ 466
ID|FBti0009066
SYM|P{lacZ}exbrl
ASTP|FBtp0001402==P{lacZ}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0004583==ex
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|P{lacZ}exbrl
ASAL|FBal0003908==exbrl
MU|P-element activity
CLOC|21C2
|Insertion site
LOCB|Proximity to gene: FBgn0004583==ex
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0003908==exbrl
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Strongest phenotypes include partial to full transformation of one or
|both eyes into antennae. Less severe adult phenotypes include excess
|bristles under the eyes, duplication of the more anterior set of scutellar
|bristles and a spoon-like curvature of the wings.
|Shows complete penetrance and variable expressivity.
PHM|eye
|vibrissae
|anterior scutellar bristle
|wing
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0009103 ICL 1 P SYM 1 P{lacZ}snunspecified ASTR 1 - CLOC 1 7D1--2 REF 1 4 DT 1 7 May 1998 RESZ 660
ID|FBti0009103
SYM|P{lacZ}snunspecified
ASTP|FBtp0001402==P{lacZ}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0003447==sn
REFDSR
{
RDID|FBrf0030136
|Mohler
|1977
PHC|female sterile | recessive
|lethal | embryonic stage | maternal effect | recessive
}
REFDSR
{
RDID|FBrf0065495
|Misra et al.
|1993
SYN|P{lacZ}snunspecified
ASAL|FBal0035639==snunspecified
CLOC|7D1--2
|Insertion site
LOCB|Proximity to gene: FBgn0003447==sn
}
REF
{
REFM|FBrf0030136
|Mohler
|1977
REFM|FBrf0065495
|Misra et al.
|1993
REFM|FBrf0091172
|Simmons et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0035639==snunspecified
REFDSR
{
RDID|FBrf0030136
|Mohler
|1977
PHP|Homozygous females lay eggs with abnormal dorsal appendages that fail
|to hatch.
PHM|dorsal appendage
|egg | maternal effect
}
REF
{
REFM|FBrf0030136
|Mohler
|1977
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0009109 ICL 1 P SYM 1 P{lacZ}trhET ASTR 1 - CLOC 1 61C1 REF 1 2 DT 1 7 May 1998 RESZ 467
ID|FBti0009109
SYM|P{lacZ}trhET
ASTP|FBtp0001402==P{lacZ}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0003749==trh
REFDSR
{
RDID|FBrf0078709
|Issac and Andrew
|1995
SYN|P{lacZ}trhET
ASAL|FBal0035844==trhET
CLOC|61C1
|Insertion site
LOCB|Proximity to gene: FBgn0003749==trh
PHC|lethal | recessive
}
REF
{
REFM|FBrf0078709
|Issac and Andrew
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0035844==trhET
REFDSR
{
RDID|FBrf0078709
|Issac and Andrew
|1995
PHP|Trachea are absent, filzkorper fail to elongate. Salivary duct cells
|fail to invaginate to form tubes.
PHM|trachea
|filzkorper
|larval salivary gland duct & embryo
}
REF
{
REFM|FBrf0078709
|Issac and Andrew
|1995
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0009111 ICL 1 P SYM 1 P{lacZ}vasunspecified ASTR 1 - CLOC 1 35B10--C1 REF 1 4 DT 1 7 May 1998 RESZ 790
ID|FBti0009111
SYM|P{lacZ}vasunspecified
ASTP|FBtp0001402==P{lacZ}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0003970==vas
REFDSR
{
RDID|FBrf0049878
|Schupbach and Wieschaus
|1989
PHC|female sterile | recessive
|lethal | embryonic stage | recessive | maternal effect
}
REFDSR
{
RDID|FBrf0051973
|Ashburner et al.
|1990
PHC|lethal | maternal effect
}
REFDSR
{
RDID|FBrf0091172
|Simmons et al.
|1996
SYN|P{lacZ}vasunspecified
ASAL|FBal0035897==vasunspecified
CLOC|35B10--C1
|Insertion site
LOCB|Proximity to gene: FBgn0003970==vas
}
REF
{
REFM|FBrf0049878
|Schupbach and Wieschaus
|1989
REFM|FBrf0051973
|Ashburner et al.
|1990
REFM|FBrf0091172
|Simmons et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0035897==vasunspecified
REFDSR
{
RDID|FBrf0045941
|Tearle and Nusslein-Volhard
|1987
PHP|Embryos derived from FBal0035897==vasunspecified mutant females
| lack pole cells,
|pole plasm and abdominal segments. Eggs are also an abnormal shape.
PHM|pole cell
|pole plasm
|egg
|embryonic abdominal segment 1
|embryonic abdominal segment 2
|embryonic abdominal segment 3
|embryonic abdominal segment 4
|embryonic abdominal segment 5
|embryonic abdominal segment 6
|embryonic abdominal segment 7
|embryonic abdominal segment 8
|embryonic abdominal segment 9
|embryonic abdominal segment 10
|embryonic abdominal segment 11
}
REFDSR
{
RDID|FBrf0049878
|Schupbach and Wieschaus
|1989
PHP|Eggs derived from homozygous females show a "grandchildless knirps-like"
|phenotype; they lack polar granules and pole cells and show deletions
|of abdominal segments similar to that seen in FBgn0001320==kni mutant embryos.
PHM|pole granule | maternal effect
|pole cell | maternal effect
|embryonic abdominal segment | maternal effect
}
REFDSR
{
RDID|FBrf0104438
|Ghabrial et al.
|1998
PHP|Condensation of DNA in the oocyte nucleus to form the karyosome is
|abnormal in homozygous egg chambers. In some cases the DNA is more
|diffuse than normal or it is threadlike and fragmented.
PHM|karyosome
}
REFDSR
{
RDID|FBrf0111879
|Ghabrial and Schupbach
|1999
PHM|karyosome
}
REF
{
REFM|FBrf0045941
|Tearle and Nusslein-Volhard
|1987
REFM|FBrf0049878
|Schupbach and Wieschaus
|1989
REFM|FBrf0104438
|Ghabrial et al.
|1998
REFM|FBrf0111879
|Ghabrial and Schupbach
|1999
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0009112 ICL 1 P SYM 1 P{lacZ}wget ASTR 1 - CLOC 1 27F1 REF 1 3 DT 1 7 May 1998 RESZ 631
ID|FBti0009112
SYM|P{lacZ}wget
SYN|wg-lacZ
ASTP|FBtp0001402==P{lacZ}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0004009==wg
|FBgn0014447==Ecol\lacZ
REFDSR
{
RDID|FBrf0058091
|Cohen et al.
|1993
SYN|P{lacZ}wget
ASAL|FBal0147926==Ecol\lacZwg-et
|FBal0033180==wget
CLOC|27F1
|Insertion site
LOCB|Proximity to gene: FBgn0004009==wg
}
REFDSR
{
RDID|FBrf0149132
|Ryoo et al.
|2002
SYN|wg-lacZ
}
REF
{
REFM|FBrf0058091
|Cohen et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0149132
|Ryoo et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0009133 ICL 1 P SYM 1 P{lacZ}svpw+ ASTR 1 - CLOC 1 87B4--5 REF 1 3 DT 1 7 May 1998 RESZ 581
ID|FBti0009133
SYM|P{lacZ}svpw+
ASTP|FBtp0001402==P{lacZ}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0003651==svp
|FBgn0014447==Ecol\lacZ
REFDSR
{
RDID|FBrf0073371
|Hoshizaki et al.
|1994
SYN|P{lacZ}svpw+
ASAL|FBal0041986==Ecol\lacZsvp-w+
|FBal0040005==svpw+
CLOC|87B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0003651==svp
}
REF
{
REFM|FBrf0073371
|Hoshizaki et al.
|1994
REFM|FBrf0083200
|Hoshizaki et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0009494 ICL 1 P SYM 1 P{lacZ}SGT ASTR 1 - CLOC 1 - REF 1 2 DT 1 7 May 1998 RESZ 356
ID|FBti0009494
SYM|P{lacZ}SGT
ASTP|FBtp0001402==P{lacZ}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0014447==Ecol\lacZ
REFDSR
{
RDID|FBrf0093054
|Bradley and Andrew
|1997
SYN|P{lacZ}SGT
ASAL|FBal0060278==Ecol\lacZSGT
}
REF
{
REFM|FBrf0093054
|Bradley and Andrew
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0009562 ICL 1 P SYM 1 P{lacZ}NMLz ASTR 1 - CLOC 1 3C7--9 REF 1 5 DT 1 31 Jan 2002 RESZ 1033
ID|FBti0009562
SYM|P{lacZ}NMLz
SYN|N-lacZ
|PlacZNMLz
|P{lacZ}MLz
|P{lacZ}NMLz
ASTP|FBtp0001402==P{lacZ}
DT|31 Jan 2002
|7 May 1998
ICL|P
ID2|FBti0009498
ASGN|FBgn0004647==N
|FBgn0014447==Ecol\lacZ
REFDSR
{
RDID|FBrf0092741
|de Celis
|1997
SYN|P{lacZ}MLz
ASAL|FBal0060283==Ecol\lacZN-MLz
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REFDSR
{
RDID|FBrf0093808
|de Celis et al.
|1997
SYN|P{lacZ}NMLz
ASAL|FBal0061710==NMLz
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REFDSR
{
RDID|FBrf0144791
|Pavlopoulos et al.
|2001
SYN|N-lacZ
|PlacZNMLz
}
REFDSR
{
RDID|FBrf0180171
|Hori et al.
|2004
SYN|N-lacZ
}
REF
{
REFM|FBrf0092741
|de Celis
|1997
REFM|FBrf0093808
|de Celis et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0144791
|Pavlopoulos et al.
|2001
REFM|FBrf0180171
|Hori et al.
|2004
}
}
# EOR
TIR
{
RETE|ID 1 FBti0009579 ICL 1 P SYM 1 P{lacZ}egr ASTR 1 - CLOC 1 - REF 1 2 DT 1 7 May 1998 RESZ 346
ID|FBti0009579
SYM|P{lacZ}egr
ASTP|FBtp0001402==P{lacZ}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0014447==Ecol\lacZ
REFDSR
{
RDID|FBrf0064552
|Kojima et al.
|1993
SYN|P{lacZ}egr
ASAL|FBal0062619==Ecol\lacZegr
}
REF
{
REFM|FBrf0064552
|Kojima et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0009597 ICL 1 P SYM 1 P{lacZ}SC ASTR 1 - CLOC 1 - REF 1 3 DT 1 7 May 1998 RESZ 408
ID|FBti0009597
SYM|P{lacZ}SC
ASTP|FBtp0001402==P{lacZ}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0014447==Ecol\lacZ
REFDSR
{
RDID|FBrf0053789
|Stuttem and Campos-Ortega
|1991
SYN|P{lacZ}SC
ASAL|FBal0063958==Ecol\lacZSC
}
REF
{
REFM|FBrf0053789
|Stuttem and Campos-Ortega
|1991
REFM|FBrf0055867
|Luer and Technau
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0009734 ICL 1 P SYM 1 P{lacZ}RBG ASTR 1 - CLOC 1 - REF 1 2 DT 1 7 May 1998 RESZ 350
ID|FBti0009734
SYM|P{lacZ}RBG
ASTP|FBtp0001402==P{lacZ}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0014447==Ecol\lacZ
REFDSR
{
RDID|FBrf0078208
|Choi and Benzer
|1993
SYN|P{lacZ}RBG
ASAL|FBal0082641==Ecol\lacZRBG
}
REF
{
REFM|FBrf0078208
|Choi and Benzer
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0009828 ICL 1 P SYM 1 P{lacW}coltP ASTR 1 - CLOC 1 23A5 REF 1 2 DT 1 7 May 1998 RESZ 668
ID|FBti0009828
SYM|P{lacW}coltP
ASTP|FBtp0000204==P{lacW}
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|FBgn0019830==colt
ARGS|FBgn0019830
REFDSR
{
RDID|FBrf0099765
|Hartenstein et al.
|1997
SYN|P{lacW}coltP
ASAL|FBal0083032==coltP
CLOC|23A5
|Insertion site
LOCB|Proximity to gene: FBgn0019830==colt
PHC|female sterile | poor
|semi-lethal | recessive
CC|Orientation of FBtp0000204==P{lacW} element is 5' to 3' relative to transcription (5'
| to 3') of FBgn0019830==colt.
}
REF
{
REFM|FBrf0099765
|Hartenstein et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0083032==coltP
REFDSR
{
RDID|FBrf0099765
|Hartenstein et al.
|1997
PHP|Mutation causes semi-lethality with death of a high proportion of first
|instar larvae, allowing 20% of mutants to emerge from the pupal case.
|Adult escapers are characterized by partially unfolded wings with
|loss of venation and reduced size (more in their width than their length).
|Wing phenotype may vary from nearly normal wings to warped wings with
|a rough texture reflecting a higher density of trichomes. Escapers
|also exhibit poor viability and sterility, 25% of females give rise
|... (see FBal0083032==coltP report)
PHM|embryonic/larval tracheal system
|wing
|wing vein
|wing & trichome
}
REF
{
REFM|FBrf0099765
|Hartenstein et al.
|1997
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0009829 ICL 1 P SYM 1 P{lacW}pumbem ASTR 1 - CLOC 1 85C4--D1 REF 1 2 DT 1 14 Oct 2001 RESZ 525
ID|FBti0009829
SYM|P{lacW}pumbem
SYN|P{lacW}bem1
ASTP|FBtp0000204==P{lacW}
DT|14 Oct 2001
|7 May 1998
ICL|P
ASGN|FBgn0003165==pum
SK|FBst0006782
|w[*]; P{w[+mC]=lacW}pum[bem]/TM6
|Total=1
REFDSR
{
RDID|FBrf0085988
|Stern et al.
|1995
SYN|P{lacW}bem1
ASAL|FBal0083062==pumbem
CLOC|85C4--D1
|Insertion site
LOCB|Proximity to gene: FBgn0003165==pum
}
REF
{
REFM|FBrf0085988
|Stern et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0083062==pumbem
REFDSR
{
RDID|FBrf0085988
|Stern et al.
|1995
PHP|Flies exhibit greatly reduced coordination, flight ability and fertility.
|Mutation affects synaptic transmission at the larval neuromuscular
|junction via an affect on excitability in the motor neuron: the mutation
|acts presynaptically to cause increased transmitter release. Larvae
|exhibit a more rapid onset of augmentation than FBgn0003165==pum+ larvae.
PHM|neuromuscular junction
}
REFDSR
{
RDID|FBrf0151333
|Schweers et al.
|2002
PHP|FBal0083062==pumbem/FBal0014078==pum7 and
| FBal0083062==pumbem/FBal0014080==pum9
| transheterozygotes exhibit
|a significantly faster long term facilitation (LTF) at the neuromuscular
|junction than seen in wild-type. Larvae also respond to nerve stimuli
|with excitatory junctional potentials (ejp's) about 95% of time
|(as compared to about 80% in controls) in low Ca2+ (0.15mM) conditions.
|At 0.10mM Ca2+ an ejp response is seen about 85% of the time (as
|compared to about 35% in controls).
}
REF
{
REFM|FBrf0085988
|Stern et al.
|1995
REFM|FBrf0151333
|Schweers et al.
|2002
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0010381 ICL 1 P SYM 1 P{lArB}chsB ASTR 1 - CLOC 1 - REF 1 2 DT 1 19 Jun 1998 RESZ 339
ID|FBti0010381
SYM|P{lArB}chsB
ASTP|FBtp0000160==P{lArB}
DT|19 Jun 1998
|19 Jun 1998
ICL|P
ASGN|FBgn0014447==Ecol\lacZ
REFDSR
{
RDID|FBrf0100917
|Siddiqi
|1998
SYN|P{lArB}chsB
ASAL|FBal0088974==Ecol\lacZchsB
}
REF
{
REFM|FBrf0100917
|Siddiqi
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0010382 ICL 1 P SYM 1 P{lArB}chsA ASTR 1 - CLOC 1 - REF 1 2 DT 1 19 Jun 1998 RESZ 339
ID|FBti0010382
SYM|P{lArB}chsA
ASTP|FBtp0000160==P{lArB}
DT|19 Jun 1998
|19 Jun 1998
ICL|P
ASGN|FBgn0014447==Ecol\lacZ
REFDSR
{
RDID|FBrf0100917
|Siddiqi
|1998
SYN|P{lArB}chsA
ASAL|FBal0088975==Ecol\lacZchsA
}
REF
{
REFM|FBrf0100917
|Siddiqi
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0010665 ICL 1 P SYM 1 P{lacW}T's ASTR 1 - CLOC 1 - REF 1 2 DT 1 26 Aug 1998 RESZ 347
ID|FBti0010665
SYM|P{lacW}T's
SYN|P{lacW}T's
ASTP|FBtp0000204==P{lacW}
DT|26 Aug 1998
|26 Aug 1998
ICL|P
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0102846
|Netter et al.
|1998
SYN|P{lacW}T's
ASAL|FBal0090054==wT's
}
REF
{
REFM|FBrf0102846
|Netter et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0090054==wT's
REFDSR
{
RDID|FBrf0102846
|Netter et al.
|1998
PHP|Pigmented area corresponds to dorsal half of the eye, with a pigmentation
|level ranging from orange to red. Ventral section of eye is white.
PHM|pigment cell
}
REF
{
REFM|FBrf0102846
|Netter et al.
|1998
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0010674 ICL 1 P SYM 1 P{lacW}mozUK ASTR 1 - CLOC 1 21--60 REF 1 2 DT 1 26 Aug 1998 RESZ 475
ID|FBti0010674
SYM|P{lacW}mozUK
ASTP|FBtp0000204==P{lacW}
DT|26 Aug 1998
|26 Aug 1998
ICL|P
ASGN|FBgn0024853==moz
REFDSR
{
RDID|FBrf0102829
|Fabrizio et al.
|1998
SYN|P{lacW}mozUK
ASAL|FBal0090221==mozUK
CLOC|21--60
|Insertion site
LOCB|Proximity to gene: FBgn0024853==moz
PHC|male sterile | recessive
}
REF
{
REFM|FBrf0102829
|Fabrizio et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0090221==mozUK
REFDSR
{
RDID|FBrf0102829
|Fabrizio et al.
|1998
PHP|Mutants show male sterility, with highly elongated, immobile, blebbed
|sperm tails and abnormal nuclear morphology. Nuclei are incompletely
|condensed and irregularly shaped. Construction of an individualization
|complex is attempted.
PHM|spermatozoon
|primary spermatocyte cyst
|spermatid & nucleus
}
REF
{
REFM|FBrf0102829
|Fabrizio et al.
|1998
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0010693 ICL 1 P SYM 1 P{PZ}amnchpd ASTR 1 - CLOC 1 18F4--19A2 REF 1 2 DT 1 26 Aug 1998 RESZ 444
ID|FBti0010693
SYM|P{PZ}amnchpd
ASTP|FBtp0000210==P{PZ}
DT|26 Aug 1998
|26 Aug 1998
ICL|P
ASGN|FBgn0000076==amn
REFDSR
{
RDID|FBrf0102808
|Moore et al.
|1998
SYN|P{PZ}amnchpd
ASAL|FBal