FlyBase Allele Report: Dmel\w[sp1]

General Information

Symbol

Dmel\w^sp1

Species

D. melanogaster

Name

spotted

FlyBase ID

FBal0018302

Feature type

allele

Associated gene

Dmel\w

Associated Insertion(s)

roo{}w^sp1

Carried in Construct

Also Known As

w^sp, sp-w

Key Links

Genomic Maps

JBrowse

Allele class

hypomorphic allele - genetic evidence

Mutagen

spontaneous

Nature of the Allele

Allele class

hypomorphic allele - genetic evidence

(Rabinow and Birchler, 1990)

Mutagen

spontaneous

(Rabinow et al., 1991, Collins et al., 1983, Zachar and Bingham, 1982)

Progenitor genotype

Associated Insertion(s)

roo{}w^sp1

Cytology

Description

Insertion of a roo element into the 5' regulatory region.

(Bhadra et al., 1997)

roo insertion in 5' regulatory region.

(Bhadra and Birchler, 1996, Chapman and Bingham, 1985)

roo insertion at nucleotide position +4922.

(Larsson et al., 1996)

roo insertion into 5' regulatory region.

(Csink et al., 1994)

Insertion of a roo element in the 5' regulatory region.

(Sabl and Birchler, 1993)

Insertion of a roo element into the 5' cis-acting regulatory sequences of w.

(Birchler, 1992)

Insertion of roo element at +4922.

(Dalby and O'Hare, 1991)

roo insertion in 5' regulatory region.

(Rabinow et al., 1991, Birchler and Hiebert, 1989)

roo insertion in the 5' cis regulatory region.

(Rabinow and Birchler, 1989)

roo insertion at nucleotide position -1170.

(Davison et al., 1985)

Insertion of a 9.2 kb roo-element at map position +4.9 relative to the transcription start site of w.

(Collins et al., 1983)

roo insertion within the w locus.

(Zachar and Bingham, 1982)

The w^sp1 region has been cloned (Zachar and Bingham, 1982) and sequenced (O'Hare, Murphy, Levis and Rubin, 1984); it is located 1.0-1.9 kb upstream from the 5' end of the start of w⁺ transcription (Zachar and Bingham, 1982; O'Hare, Levis and Rubin, 1983). w^sp1 shows sequence homology and behavior analogous to enhancer sequences (Davison, Chapman, Wedeen and Bingham, 1985). The lesions responsible for w^sp1, w^sp2 and w^sp4 have been analyzed by sequencing cloned portions of these alleles; the breakpoints of w^sp3 and w^sp81d have also been established by molecular methods. w^sp1 carries roo; the other alleles are molecular deletions. Sensitivity to the effect of su(w^sp) on eye pigmentation is deleted by w^sp81d but not by w^sp3 (Davison, Chapman, Wedeen and Bingham, 1985). 8.7 kb insertion map site (kb): +4.92; Origin = insertion of w^a copia; '-' values to left (telomere) end; '+' values to right (centromere) end. In spite of the variegated pattern of spots in the eye in this mutant, the transcript is like that of w⁺ in size, structure and amount (Levis et al., 1984; Pirrotta and Brockl, 1984).

Mutations Mapped to the Genome

Curation Data

Type

Location

Additional Notes

References

transposable_element_insertion_site

X:2,797,708..2,797,712 [-]

(Frolov et al., 1998, Soriano et al., 1998, Bhadra et al., 1997, Bhadra et al., 1997, Bhadra and Birchler, 1996, Larsson et al., 1996, Sabl and Birchler, 1993, Birchler, 1992, Dalby and O'Hare, 1991, Rabinow et al., 1991, Rabinow and Birchler, 1989, Chapman and Bingham, 1985, Davison et al., 1985, Collins et al., 1983, Zachar and Bingham, 1982)

Variant Molecular Consequences

Associated Sequence Data

DDBJ / EMBL / GenBank

DNA sequence

Protein sequence

X02776

UniProtKB/Swiss-Prot

UniProtKB/TrEMBL

Expression Data

Reporter Expression

Additional Information

Statement

Reference

Marker for

Reflects expression of

Reporter construct used in assay

Human Disease Associations

Disease Ontology (DO) Annotations

Models Based on Experimental Evidence ( 0 )

Disease

Evidence

References

Modifiers Based on Experimental Evidence ( 0 )

Disease

Interaction

References

Comments on Models/Modifiers Based on Experimental Evidence ( 0 )

Disease-implicated variant(s)

Phenotypic Data

Phenotypic Class

Phenotype Manifest In

eye | pharate adult stage

(Wasser and Chia, 2007)

pigment cell

(Benevolenskaya et al., 1998, Frolov et al., 1998, Lefevre and Wilkins, 1966)

testis pigment cell

Detailed Description

Statement

Reference

Eye pigmentation is reduced in pharate adults.

(Wasser and Chia, 2007)

Homozygous males are darker than homozygous females. Triple X metafemale individuals homozygous for w^sp1 exhibit a lighter eye colour than w^sp1 homozygous XX females.

(Birchler, 1992)

Eye colour: uniformly coloured as w^sp1/w^e59; darker than either homozygous w^sp1 or homozygous w^e59 females.

(Dalby and O'Hare, 1991)

Testis colour: pigmentation enhanced.

(Judd, 1987, Davison et al., 1985, Pirrotta et al., 1985)

Eye colour: relatively light, non-uniform distribution of eye colour.

(Lefevre and Wilkins, 1966)

Eye colour: homogenous brown, with w¹. Eye colour: homogenous brown, with w^ch. Eye colour: homogenous brown, with w^a.

(Green, 1959)

Eye colour: white, as w^a w^sp1. Eye colour: pale yellow, as w^ch w^sp1. Eye colour: like w^sp1 when heterozygous with w^-.

(Green, 1959)

Eye colour: yellowish to brown; fine-grained mottling; male darker than female. Eye colour: yellow, in females with z¹, and two synapsed copies of w^sp1 in trans (or tandemly repeated). Malpighian tubule colour: wild-type. Affects that deposition of the eye pigments, resulting in a variegated phenotype.

External Data

Linkouts

Interactions

Show genetic interaction network for Enhancers & Suppressors

Phenotypic Class

Enhanced by

Statement

Reference

w^sp1 has abnormal eye color phenotype, enhanceable by z^v77h

(Georgiev, 1994)

w^sp1 has abnormal eye color phenotype, enhanceable by z¹

(Georgiev, 1994)

w^sp1, z^v77h has abnormal eye color phenotype, enhanceable by Taf9¹

(Georgiev, 1994)

w^sp1, z¹ has abnormal eye color phenotype, enhanceable by Taf9¹

(Georgiev, 1994)

w^sp1, z^v77h has abnormal eye color phenotype, enhanceable by e(y)2¹

(Georgiev, 1994)

w^sp1, z^v77h has abnormal eye color phenotype, enhanceable by e(y)3⁴

(Georgiev, 1994)

w^sp1, z¹ has abnormal eye color phenotype, enhanceable by e(y)3⁴

(Georgiev, 1994)

w^sp1, z^op6 has abnormal eye color phenotype, enhanceable by e(y)3⁴

(Georgiev, 1994)

w^sp1, z^op6R1 has abnormal eye color phenotype, enhanceable by e(y)3⁴

(Georgiev, 1994)

NOT Enhanced by

Statement

Reference

w^sp1, z¹ has abnormal eye color phenotype, non-enhanceable by e(y)2¹

(Georgiev, 1994)

Suppressed by

Statement

Reference

w^sp1 has abnormal eye color | pharate adult stage phenotype, suppressible by east¹/east¹

(Wasser and Chia, 2007)

w^sp1 has visible | pharate adult stage phenotype, suppressible by east¹/east¹

(Wasser and Chia, 2007)

w^sp1 has abnormal eye color | pharate adult stage phenotype, suppressible by east^hop-7/east^hop-7

(Wasser and Chia, 2007)

w^sp1 has visible | pharate adult stage phenotype, suppressible by east^hop-7/east^hop-7

(Wasser and Chia, 2007)

w^sp1 has abnormal eye color | pharate adult stage phenotype, suppressible by east¹/east^hop-7

(Wasser and Chia, 2007)

w^sp1 has visible | pharate adult stage phenotype, suppressible by east¹/east^hop-7

(Wasser and Chia, 2007)

w^sp1 has abnormal eye color | pharate adult stage phenotype, suppressible by su(w[sp])[+]/east¹

(Wasser and Chia, 2007)

w^sp1 has visible | pharate adult stage phenotype, suppressible by su(w[sp])[+]/east¹

(Wasser and Chia, 2007)

w^sp1 has abnormal eye color | pharate adult stage phenotype, suppressible by east^hop-7/east[+]

(Wasser and Chia, 2007)

w^sp1 has visible | pharate adult stage phenotype, suppressible by east^hop-7/east[+]

(Wasser and Chia, 2007)

w^sp1 has abnormal eye color | recessive phenotype, suppressible by Rga[+]/Rga⁰³⁸³⁴

(Frolov et al., 1998)

w^sp1 has abnormal eye color phenotype, suppressible by east^R63

(Soriano et al., 1998)

Phenotype Manifest In

Enhanced by

Statement

Reference

w^sp1 has phenotype, enhanceable by Ufo¹

(Bhadra et al., 1998)

w^sp1 has phenotype, enhanceable by Wow^unspecified

(Bhadra et al., 1998)

w^sp1 has phenotype, enhanceable by Wow^unspecified/Low¹

(Bhadra et al., 1998)

w^sp1 has phenotype, enhanceable by Low¹/Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, enhanceable by Wow^unspecified/Ufo¹

(Bhadra et al., 1998)

w^sp1 has phenotype, enhanceable by Ufo¹/Mow^EMS

(Bhadra et al., 1998)

w^sp1 has phenotype, enhanceable by Wow^unspecified/Mow^EMS/Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, enhanceable by Wow^unspecified/Mow^EMS/Low¹/Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has pigment cell phenotype, enhanceable by RpLP0⁰¹⁵⁴⁴

(Frolov and Birchler, 1998)

w^sp1 has phenotype, enhanceable by Wow^γb

(Birchler et al., 1994)

w^sp1 has phenotype, enhanceable by Wow^γe

(Birchler et al., 1994)

w^sp1 has phenotype, enhanceable by Wow^ems1

(Birchler et al., 1994)

w^sp1 has phenotype, enhanceable by Wow^hd1

(Birchler et al., 1994)

w^sp1 has phenotype, enhanceable by Taf9¹

(Georgiev, 1994)

w^sp1 has phenotype, enhanceable by e(y)3⁴

(Georgiev, 1994)

w^sp1 has pigment cell phenotype, enhanceable by z^v77h

(Georgiev, 1994)

w^sp1 has pigment cell phenotype, enhanceable by z¹

(Georgiev, 1994)

w^sp1, z^v77h has pigment cell phenotype, enhanceable by Taf9¹

(Georgiev, 1994)

w^sp1, z¹ has pigment cell phenotype, enhanceable by Taf9¹

(Georgiev, 1994)

w^sp1, z^v77h has pigment cell phenotype, enhanceable by e(y)2¹

(Georgiev, 1994)

w^sp1, z^v77h has pigment cell phenotype, enhanceable by e(y)3⁴

(Georgiev, 1994)

w^sp1, z¹ has pigment cell phenotype, enhanceable by e(y)3⁴

(Georgiev, 1994)

w^sp1, z^op6 has pigment cell phenotype, enhanceable by e(y)3⁴

(Georgiev, 1994)

w^sp1, z^op6R1 has pigment cell phenotype, enhanceable by e(y)3⁴

(Georgiev, 1994)

w^sp1 has phenotype, enhanceable by Ts(YLt;2Rt)L52+Ts(YLt;2Lt)R15

(Sabl and Birchler, 1993)

w^sp1 has phenotype, enhanceable by Ts(YSt;2Rt)B4+Ts(YLt;2Lt)H174

(Sabl and Birchler, 1993)

w^sp1 has phenotype, enhanceable by Ts(YLt;2Rt)B110+Ts(YLt;2Lt)L138

(Sabl and Birchler, 1993)

w^sp1 has phenotype, enhanceable by Ts(YLt;2Rt)G10+Ts(YLt;2Lt)R155

(Sabl and Birchler, 1993)

w^sp1 has phenotype, enhanceable by Dp(2;Y)J64

(Sabl and Birchler, 1993)

w^sp1 has phenotype, enhanceable by Ts(YLt;3Lt)B116+Ts(YLt;3Rt)G48

(Sabl and Birchler, 1993)

w^sp1 has phenotype, enhanceable by Ts(YSt;3Rt)G73+Ts(YSt;3Lt)R128

(Sabl and Birchler, 1993)

NOT Enhanced by

Statement

Reference

w^sp1 has phenotype, non-enhanceable by Kr-h1⁰⁵²⁰⁸

(Benevolenskaya et al., 2000)

w^sp1 has phenotype, non-enhanceable by Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, non-enhanceable by Low¹

(Bhadra et al., 1998, Bhadra et al., 1997)

w^sp1 has phenotype, non-enhanceable by Wow^unspecified/Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, non-enhanceable by Mow^EMS/Low¹

(Bhadra et al., 1998)

w^sp1 has phenotype, non-enhanceable by Wow^unspecified/Low¹/Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, non-enhanceable by Mow^EMS/Low¹/Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, non-enhanceable by In(3)Msu¹

(Csink et al., 1994)

w^sp1 has phenotype, non-enhanceable by In(3)Msu²

(Csink et al., 1994)

w^sp1 has phenotype, non-enhanceable by Rm62^D

(Csink et al., 1994)

w^sp1 has phenotype, non-enhanceable by Rm62^Dem

(Csink et al., 1994)

w^sp1 has phenotype, non-enhanceable by Rm62^E

(Csink et al., 1994)

w^sp1 has phenotype, non-enhanceable by Rm62^F

(Csink et al., 1994)

w^sp1 has phenotype, non-enhanceable by Rm62^H

(Csink et al., 1994)

w^sp1 has phenotype, non-enhanceable by Rm62^K

(Csink et al., 1994)

w^sp1, z¹ has pigment cell phenotype, non-enhanceable by e(y)2¹

(Georgiev, 1994)

w^sp1 has phenotype, non-enhanceable by Ts(YLt;2Lt)R14+Ts(YSt;2Rt)L110

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-enhanceable by Ts(YSt;2Lt)H149+Ts(YSt;2Rt)R14

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-enhanceable by Ts(YSt;2Rt)L107+Ts(YSt;2Lt)P59

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-enhanceable by Ts(YLt;3Lt)B141

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-enhanceable by Ts(YSt;3Rt)B141+Ts(YSt;3Lt)G122

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-enhanceable by Ts(YLt;3Lt)A31+Ts(YLt;3Rt)G122

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-enhanceable by Ts(YSt;3Lt)G48+Ts(YSt;3Rt)R36

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-enhanceable by Ts(YSt;2Lt)B110+Ts(YSt;2Rt)R15

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-enhanceable by Ts(YSt;2Lt)D20+Ts(YSt;2Rt)L138

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-enhanceable by Ts(YSt;2Lt)L23+Ts(YSt;2Rt)R155

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-enhanceable by E(w^a)¹

(Birchler and Hiebert, 1989)

Suppressed by

Statement

Reference

w^sp1 has eye | pharate adult stage phenotype, suppressible by east¹/east¹

(Wasser and Chia, 2007)

w^sp1 has eye | pharate adult stage phenotype, suppressible by east^hop-7/east^hop-7

(Wasser and Chia, 2007)

w^sp1 has eye | pharate adult stage phenotype, suppressible by east¹/east^hop-7

(Wasser and Chia, 2007)

w^sp1 has eye | pharate adult stage phenotype, suppressible by su(w[sp])[+]/east¹

(Wasser and Chia, 2007)

w^sp1 has eye | pharate adult stage phenotype, suppressible by east^hop-7/east[+]

(Wasser and Chia, 2007)

w^sp1 has phenotype, suppressible by Mow^EMS/Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, suppressible by Wow^unspecified/Mow^EMS

(Bhadra et al., 1998)

w^sp1 has phenotype, suppressible by Wow^unspecified/Mow^EMS/Low¹

(Bhadra et al., 1998)

w^sp1 has phenotype, suppressible by Mow^EMS

(Bhadra et al., 1998)

w^sp1 has pigment cell phenotype, suppressible by Rga[+]/Rga⁰³⁸³⁴

(Frolov et al., 1998)

w^sp1 has pigment cell phenotype, suppressible by east^R63

(Soriano et al., 1998)

w^sp1 has phenotype, suppressible by Ufo¹

(Bhadra et al., 1997)

w^sp1 has phenotype, suppressible by Mow^gamma

(Bhadra and Birchler, 1996)

w^sp1 has phenotype, suppressible by Ts(YLt;3Rt)R128

(Sabl and Birchler, 1993)

w^sp1 has phenotype, suppressible by east¹

(Chapman and Bingham, 1985)

NOT suppressed by

Statement

Reference

w^sp1 has phenotype, non-suppressible by Kr-h1⁰⁵²⁰⁸

(Benevolenskaya et al., 2000)

w^sp1 has phenotype, non-suppressible by Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, non-suppressible by Low¹

(Bhadra et al., 1998, Bhadra et al., 1997)

w^sp1 has phenotype, non-suppressible by Wow^unspecified/Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, non-suppressible by Mow^EMS/Low¹

(Bhadra et al., 1998)

w^sp1 has phenotype, non-suppressible by Wow^unspecified/Low¹/Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, non-suppressible by Mow^EMS/Low¹/Pcf11^EMS2

(Bhadra et al., 1998)

w^sp1 has phenotype, non-suppressible by In(3)Msu¹

(Csink et al., 1994)

w^sp1 has phenotype, non-suppressible by In(3)Msu²

(Csink et al., 1994)

w^sp1 has phenotype, non-suppressible by Rm62^D

(Csink et al., 1994)

w^sp1 has phenotype, non-suppressible by Rm62^Dem

(Csink et al., 1994)

w^sp1 has phenotype, non-suppressible by Rm62^E

(Csink et al., 1994)

w^sp1 has phenotype, non-suppressible by Rm62^F

(Csink et al., 1994)

w^sp1 has phenotype, non-suppressible by Rm62^H

(Csink et al., 1994)

w^sp1 has phenotype, non-suppressible by Rm62^K

(Csink et al., 1994)

w^sp1 has phenotype, non-suppressible by Ts(YSt;2Lt)B110+Ts(YSt;2Rt)R15

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-suppressible by Ts(YSt;2Lt)D20+Ts(YSt;2Rt)L138

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-suppressible by Ts(YSt;2Lt)L23+Ts(YSt;2Rt)R155

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-suppressible by Ts(YLt;2Lt)R14+Ts(YSt;2Rt)L110

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-suppressible by Ts(YSt;2Lt)H149+Ts(YSt;2Rt)R14

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-suppressible by Ts(YSt;2Rt)L107+Ts(YSt;2Lt)P59

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-suppressible by Ts(YLt;3Lt)B141

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-suppressible by Ts(YSt;3Rt)B141+Ts(YSt;3Lt)G122

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-suppressible by Ts(YLt;3Lt)A31+Ts(YLt;3Rt)G122

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-suppressible by Ts(YSt;3Lt)G48+Ts(YSt;3Rt)R36

(Sabl and Birchler, 1993)

w^sp1 has phenotype, non-suppressible by Pcf11^γb

(Rabinow et al., 1991)

w^sp1 has phenotype, non-suppressible by Pcf11^γc

(Rabinow et al., 1991)

w^sp1 has phenotype, non-suppressible by Pcf11^γd

(Rabinow et al., 1991)

w^sp1 has phenotype, non-suppressible by Pcf11^EMS3

(Rabinow et al., 1991)

w^sp1 has phenotype, non-suppressible by Pcf11^EMS4

(Rabinow et al., 1991)

w^sp1 has phenotype, non-suppressible by Pcf11^EMS5

(Rabinow et al., 1991)

w^sp1 has phenotype, non-suppressible by Pcf11^hd1

(Rabinow et al., 1991)

w^sp1 has phenotype, non-suppressible by Pcf11^γsc

(Rabinow et al., 1991)

w^sp1 has phenotype, non-suppressible by mw²

(Rabinow and Birchler, 1990)

Other

Statement

Reference

sgl⁰⁵⁰⁰⁷, w^sp1 has pigment cell phenotype

(Benevolenskaya et al., 1998)

Additional Comments

Genetic Interactions

Statement

Reference

Eye pigmentation of w^sp1 animals is restored to almost wild type levels in east¹ or east^hop-7 homozygotes, or east¹/east^hop-7 transheterozygotes. w^sp1 eye pigmentation is rescued to intermediate levels in east¹ or east^hop-7 heterozygotes.

(Wasser and Chia, 2007)

Transheterozygotes with su(w^sp)^R63 have more red eye pigment than w^sp1 flies.

(Soriano et al., 1998)

No interaction with mutations of Rm62.

(Csink et al., 1994)

Xenogenetic Interactions

Statement

Reference

Complementation and Rescue Data

Partially complements

w^e59

(Dalby and O'Hare, 1991)

w^unspecified

(Lefevre and Wilkins, 1966)

w^ch

(Green, 1959)

w^a

(Green, 1959)

w¹

(Green, 1959)

Fails to complement

w^66A

(Pastink et al., 1987)

w^53A

(Pastink et al., 1987)

w⁴⁹

(Pastink et al., 1987)

w^30C

(Pastink et al., 1987)

Comments

w^sp1/w^unspecified flies have dark, but not wild-type colour eyes.

(Lefevre and Wilkins, 1966)

Complementation synapsis-dependent.

(Green, 1959)

Images (2)

Holtzman, S. and Kaufman, T. (2013)

Mutant

Wild-type

Stocks (4)

Bloomington

64170

P{NA}1A w^sp1 |P-cytotype|

6038

y² sc¹ east¹ w^sp1/FM7c

Kyoto

101266

y² sc¹ w^sp1

101024

C(1)DX, y¹ w¹ f¹ / Dp(1;1)w^sp, sc¹ z¹ w^sp1 ec¹

Notes on Origin

Discoverer

Showell, 1944.

Comments

Located proximal to w^ch and distal to w^DZL.

Frequency of reversion of the 8.7kb roo insertion in both somatic tissue and the germline after larval exposure to three different alkylating agents, EMS, ENU and MMS, is analysed. The mutagens used did not induce excision of roo, the revertant phenotypes obtained are due to second site modifiers acting on w expression.

(Soriano et al., 1998)

Shows hyper-dosage compensation.

(Qian and Pirrotta, 1995, Birchler, 1992)

External Crossreferences and Linkouts ( 1 )

Crossreferences

GenBank Nucleotide - A collection of sequences from several sources, including GenBank, RefSeq, TPA, and PDB.

X02776

Synonyms and Secondary IDs (6)

Reported As

Name Synonyms

spotted

spotted-1

(Rabinow and Birchler, 1989)

Secondary FlyBase IDs

References (54)

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