FlyBase Allele Report: Dmel\ash1[17]

General Information

Symbol

Dmel\ash1¹⁷

Species

D. melanogaster

Name

FlyBase ID

FBal0000749

Feature type

allele

Associated gene

Dmel\ash1

Associated Insertion(s)

Carried in Construct

Also Known As

ash1^VF101

Key Links

Allele class

antimorphic allele - genetic evidence

Mutagen

ethyl methanesulfonate

Nature of the Allele

Allele class

antimorphic allele - genetic evidence

(Tripoulas et al., 1996)

Mutagen

ethyl methanesulfonate

(Tripoulas et al., 1996, Tripoulas et al., 1994)

Progenitor genotype

Cytology

Description

Deletion of 451 bases between nucleotide 2483 and 2934.

(Tripoulas et al., 1996)

Mutations Mapped to the Genome

Curation Data

Type

Location

Additional Notes

References

Variant Molecular Consequences

Associated Sequence Data

DDBJ / EMBL / GenBank

DNA sequence

Protein sequence

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

lethal | recessive

(Tripoulas et al., 1994)

lethal - all die before end of larval stage | recessive

(Tripoulas et al., 1996)

some die during larval stage | recessive

(Tripoulas et al., 1996)

Phenotype Manifest In

Detailed Description

Statement

Reference

Double heterozygotes with Ubx^abx-1, trx^el2 or brm² exhibit transformation of third leg to second leg identity and haltere to wing transformation.

(Tripoulas et al., 1996)

External Data

Linkouts

Interactions

Show genetic interaction network for Enhancers & Suppressors

Phenotypic Class

Enhanced by

Statement

Reference

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Asx^XF23/Asx[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by E(Pc)[+]/E(Pc)¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by E(z)[+]/E(z)⁵

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Psc[+]/Psc¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Sce[+]/Sce^D1

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Scm^D1/Scm[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Scm^M56/Scm[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Su(z)2¹/Su(z)2[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Su(z)4[+]/Su(z)4¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Su(z)6[+]/Su(z)6¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Su(z)7[+]/Su(z)7¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Trl[+]/Trl^R85

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by mxc[+]/mxc^G48

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by sxc[+]/sxc¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Kdm5^k06801/lid[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Asx³/Asx[+]

(Gildea et al., 2000)

ash1[+]/ash1¹⁷, trx^B11 has visible | dominant | homeotic phenotype, enhanceable by lawc^p1/lawc[+]

(Zorin et al., 1999)

ash1¹⁷, trx^B11 has visible | homeotic phenotype, enhanceable by lawc^EF520

(Zorin et al., 1999)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by lawc^p1/lawc[+]

(Zorin et al., 1999)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by lawc[+]/lawc^EF520

(Zorin et al., 1999)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, enhanceable by Df(1)RA2/+

(Zorin et al., 1999)

ash1[+]/ash1¹⁷, trx^B11 has visible | dominant | homeotic phenotype, enhanceable by lawc[+]/lawc^EF520

(Zorin et al., 1999)

ash1[+]/ash1¹⁷, trx^B11 has visible | dominant | homeotic phenotype, enhanceable by Df(1)RA2/+

(Zorin et al., 1999)

ash1¹⁷, mod(mdg4)^T16/mod(mdg4)[+] has visible | dominant | homeotic phenotype, enhanceable by trx^B11/trx[+]

(Gerasimova and Corces, 1998)

ash1¹⁷, mod(mdg4)^ul has visible | homeotic phenotype, enhanceable by trx^B11

(Gerasimova and Corces, 1998)

ash1¹⁷, mod(mdg4)^T6 has visible | homeotic phenotype, enhanceable by trx^B11

(Gerasimova and Corces, 1998)

ash1[+]/ash1¹⁷, trx^B11 has visible | dominant | homeotic phenotype, enhanceable by mod(mdg4)[+]/mod(mdg4)^ul

(Gerasimova and Corces, 1998)

ash1[+]/ash1¹⁷, trx^B11 has visible | dominant | homeotic phenotype, enhanceable by mod(mdg4)[+]/mod(mdg4)^T6

(Gerasimova and Corces, 1998)

ash1[+]/ash1¹⁷, trx^B11 has visible | dominant | homeotic phenotype, enhanceable by mod(mdg4)^T16/mod(mdg4)[+]

(Gerasimova and Corces, 1998)

NOT Enhanced by

Statement

Reference

ash1¹⁷ has visible | dominant | homeotic phenotype, non-enhanceable by Df(1)RA2

(Zorin et al., 1999)

ash1¹⁷ has visible | dominant | homeotic phenotype, non-enhanceable by lawc^p1

(Zorin et al., 1999)

ash1¹⁷ has visible | dominant | homeotic phenotype, non-enhanceable by lawc^EF520

(Zorin et al., 1999)

ash1¹⁷ has visible | dominant | homeotic phenotype, non-enhanceable by lawc⁺¹⁰

(Zorin et al., 1999)

Suppressed by

Statement

Reference

ash1¹⁷, trx^B11/trx[+] has visible | dominant phenotype, suppressible | partially by His2Av⁰⁵¹⁴⁶

(Swaminathan et al., 2005)

ash1¹⁷, trx^B11/trx[+] has visible | dominant phenotype, suppressible | partially by His2Av⁸¹⁰

(Swaminathan et al., 2005)

ash1[+]/ash1¹⁷, trx^B11 has visible | dominant | homeotic phenotype, suppressible by dom¹⁴/dom[+]

(Ruhf et al., 2001)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by dom¹⁴/dom[+]

(Ruhf et al., 2001)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by Pc³/Pc[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by Pcl⁷/Pcl[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by Psc[+]/Psc^Arp1

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by Scm^Suz302/Scm[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by esc¹⁰/esc[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by esc²¹/esc[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by esc⁵/esc[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by esc⁹/esc[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by mxc[+]/mxc¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by mxc[+]/mxc^M1

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by ph-d[+]/ph-d⁵⁰³

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by pho^b/pho[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by sxc[+]/sxc⁴

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has visible | dominant | homeotic phenotype, suppressible by sxc[+]/sxc⁵

(Gildea et al., 2000)

Enhancer of

Statement

Reference

trx^B11, trx[+], ash1[+], ash1¹⁷ is an enhancer of visible | homeotic phenotype of lawc^p1

(Zorin et al., 1999)

ash1[+]/ash1¹⁷ is an enhancer of visible | dominant | homeotic phenotype of mod(mdg4)^T6, trx^B11

(Gerasimova and Corces, 1998)

Other

Statement

Reference

ash1¹⁷, trx^B11/trx[+] has visible | dominant phenotype

(Swaminathan et al., 2005)

ash1[+]/ash1¹⁷, trx^B11 has visible phenotype

(Swaminathan et al., 2005)

ash1¹⁷, trx^B11 has visible | homeotic phenotype

(Ruhf et al., 2001, Zorin et al., 1999, Gerasimova and Corces, 1998)

ash1[+]/ash1¹⁷, trx^B11 has visible | homeotic phenotype

(Ruhf et al., 2001)

ash1¹⁷, trx^B11/trx[+] has visible | homeotic phenotype

(Ruhf et al., 2001)

ash1¹⁷, lawc^p1/lawc^EF520 has lethal phenotype

(Zorin et al., 1999)

Df(1)RA2/lawc^p1, ash1¹⁷ has lethal phenotype

(Zorin et al., 1999)

Phenotype Manifest In

Enhanced by

Statement

Reference

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Asx³/Asx[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Asx^XF23/Asx[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by E(Pc)[+]/E(Pc)¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by E(z)[+]/E(z)⁵

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Psc[+]/Psc¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Sce[+]/Sce^D1

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Scm^D1/Scm[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Scm^M56/Scm[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Su(z)2¹/Su(z)2[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Su(z)4[+]/Su(z)4¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Su(z)6[+]/Su(z)6¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Su(z)7[+]/Su(z)7¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Trl[+]/Trl^R85

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by mxc[+]/mxc^G48

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by sxc[+]/sxc¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, enhanceable by Kdm5^k06801/lid[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11 has metathoracic leg phenotype, enhanceable by lawc^EF520

(Zorin et al., 1999)

ash1¹⁷, trx^B11/trx[+] has haltere phenotype, enhanceable by lawc^p1/lawc[+]

(Zorin et al., 1999)

ash1¹⁷, trx^B11/trx[+] has metathoracic leg phenotype, enhanceable by lawc^p1/lawc[+]

(Zorin et al., 1999)

ash1[+]/ash1¹⁷, trx^B11 has haltere phenotype, enhanceable by lawc^p1/lawc[+]

(Zorin et al., 1999)

ash1¹⁷, trx^B11/trx[+] has haltere phenotype, enhanceable by lawc[+]/lawc^EF520

(Zorin et al., 1999)

ash1[+]/ash1¹⁷, trx^B11 has metathoracic leg phenotype, enhanceable by lawc^p1/lawc[+]

(Zorin et al., 1999)

NOT Enhanced by

Statement

Reference

ash1¹⁷ has phenotype, non-enhanceable by Df(1)RA2

(Zorin et al., 1999)

Suppressed by

Statement

Reference

ash1¹⁷, trx^B11/trx[+] has mesothoracic tibial apical bristle | ectopic phenotype, suppressible | partially by His2Av⁰⁵¹⁴⁶

(Swaminathan et al., 2005)

ash1¹⁷, trx^B11/trx[+] has mesothoracic tibial apical bristle | ectopic phenotype, suppressible | partially by His2Av⁸¹⁰

(Swaminathan et al., 2005)

ash1¹⁷, trx^B11/trx[+] has metathoracic leg phenotype, suppressible | partially by His2Av⁰⁵¹⁴⁶

(Swaminathan et al., 2005)

ash1¹⁷, trx^B11/trx[+] has metathoracic leg phenotype, suppressible | partially by His2Av⁸¹⁰

(Swaminathan et al., 2005)

ash1[+]/ash1¹⁷, trx^B11 has abdominal segment 6 phenotype, suppressible by dom¹⁴/dom[+]

(Ruhf et al., 2001)

ash1¹⁷, trx^B11/trx[+] has abdominal segment 6 phenotype, suppressible by dom¹⁴/dom[+]

(Ruhf et al., 2001)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by Pc³/Pc[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by Pcl⁷/Pcl[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by Psc[+]/Psc^Arp1

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by Scm^Suz302/Scm[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by esc¹⁰/esc[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by esc²¹/esc[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by esc⁵/esc[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by esc⁹/esc[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by mxc[+]/mxc¹

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by mxc[+]/mxc^M1

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by ph-d[+]/ph-d⁵⁰³

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by pho^b/pho[+]

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by sxc[+]/sxc⁴

(Gildea et al., 2000)

ash1¹⁷, trx^B11/trx[+] has adult metathoracic segment phenotype, suppressible by sxc[+]/sxc⁵

(Gildea et al., 2000)

Enhancer of

Statement

Reference

ash1[+]/ash1¹⁷ is an enhancer of wing vein | ectopic phenotype of Snr1^E1

(Marenda et al., 2004)

trx^B11, trx[+], ash1[+], ash1¹⁷ is an enhancer of arista phenotype of lawc^p1

(Zorin et al., 1999)

trx^B11, trx[+], ash1[+], ash1¹⁷ is an enhancer of phenotype of mod(mdg4)^ul

(Gerasimova and Corces, 1998)

ash1[+]/ash1¹⁷ is an enhancer of haltere phenotype of mod(mdg4)^T6, trx^B11

(Gerasimova and Corces, 1998)

Suppressor of

Statement

Reference

ash1[+]/ash1¹⁷ is a suppressor of wing vein | ectopic phenotype of Snr1^E1

(Marenda et al., 2004)

Other

Statement

Reference

ash1¹⁷, trx^B11/trx[+] has metathoracic leg phenotype

(Swaminathan et al., 2005)

ash1¹⁷, trx^B11 has mesothoracic tibial apical bristle | ectopic phenotype

(Swaminathan et al., 2005)

ash1¹⁷, trx^B11/trx[+] has mesothoracic tibial apical bristle | ectopic phenotype

(Swaminathan et al., 2005)

ash1¹⁷, trx^B11 has metathoracic leg phenotype

(Swaminathan et al., 2005, Zorin et al., 1999)

ash1¹⁷, trx^B11 has abdominal segment 6 phenotype

(Ruhf et al., 2001)

ash1[+]/ash1¹⁷, trx^B11 has abdominal segment 6 phenotype

(Ruhf et al., 2001)

ash1¹⁷, trx^B11/trx[+] has abdominal segment 6 phenotype

(Ruhf et al., 2001)

ash1¹⁷, trx^B11 has haltere phenotype

(Zorin et al., 1999)

Additional Comments

Genetic Interactions

Statement

Reference

ash1¹⁷ trx^B11 double heterozygotes show transformations of third leg into second leg; an apical bristle appears on the third leg in 66% of cases. The frequency of the appearance of an apical bristle on the third leg decreases to 37% in ash1¹⁷ trx^B11 His2Av⁰⁵¹⁴⁶ triple heterozygotes and to 29% in ash1¹⁷ trx^B11 His2Av⁸¹⁰ triple heterozygotes.

(Swaminathan et al., 2005)

At 29^oC, ash1¹⁷ suppresses the ectopic vein that extends distally from the posterior crossvein in Snr1^E1 animals. but enhances the extra vein material seen posterior of the L5 wing vein.

(Marenda et al., 2004)

The abdominal segment A6 to A5 transformation of ash1¹⁷/+, trx^B11/+ is dominantly suppressed by dom¹⁴.

(Ruhf et al., 2001)

52.1% of trx^B11 ash1¹⁷ double heterozygotes show T3 to T2 transformations. The penetrance of this phenotype is enhanced by one copy of lid^k06801, E(Pc)¹, Su(z)2¹, Psc¹, Asx^XF23, Asx³, mxc^G48, sxc¹, Sce^D1, E(z)⁵, Trl^R85, Su(z)4¹, Su(z)7¹, Su(z)6¹, Scm^D1 or Scm^M56 and suppressed by one copy of Pc³, ph-d⁵⁰³, Pcl⁷, pho^b, mxc^M1, mxc¹, esc⁵, esc⁹, esc¹⁰, esc²¹, sxc⁴, sxc⁵, Psc^Arp1 or Scm^Suz302.

(Gildea et al., 2000)

The frequency of homeotic transformations in heterozygotes is not enhanced by lawc^p1, lawc^EF520, lawc⁺¹⁰ or Df(1)RA2. The frequency and severity of homeotic transformations (such as haltere to wing or third leg to second leg transformations) in trx^B11 ash1¹⁷ double heterozygotes is dominantly enhanced by lawc^p1. The enhancement is stronger in a lawc^p1 maternal background. The arista to leg transformation characteristic of lawc^p1 is also enhanced in these flies. The frequency of homeotic transformations in trx^B11 ash1¹⁷ double heterozygotes is dominantly enhanced by lawc^EF520 or Df(1)RA2. lawc^p1/lawc^EF520 females are viable. However, in combination with ash1¹⁷, lawc^p1/lawc^EF520 results in lethality. lawc^p1/Df(1)RA2 females are viable. However, in combination with ash1¹⁷, lawc^p1/Df(1)RA2 results in lethality.

(Zorin et al., 1999)

14.1% of trx^B11 ash1¹⁷ double heterozygous adults show a homeotic phenotype. This is increased to 77.7% if the flies are also heterozygous for mod(mdg4)^T16, 50.4% if the flies are also heterozygous for mod(mdg4)^ul and 32.6% if the flies are also heterozygous for mod(mdg4)^T6. The combination ash1¹⁷ trx^B11 dominantly enhances the effect of mod(mdg4)^ul on the y² phenotype.

(Gerasimova and Corces, 1998)

Xenogenetic Interactions

Statement

Reference

Complementation and Rescue Data

Comments

Images (0)

Mutant

Wild-type

Stocks (0)

Notes on Origin

Discoverer

Comments

Range of lethality for transheterozygotes extends from the third larval instar for the most severe alleles to the pharate adult stage for the least severe alleles.

(Tripoulas et al., 1994)

External Crossreferences and Linkouts ( 0 )

Synonyms and Secondary IDs (7)

Reported As

Symbol Synonym

VF101

ash-1^VF101

(Zorin et al., 1999)

ash1¹⁷

ash1^VF101

(Swaminathan et al., 2005, Gildea et al., 2000, Gerasimova and Corces, 1998)

ash¹⁷

(Ruhf et al., 2001)

dash¹⁷

(Lindsley and Zimm, 1992)

dash^VF101

(Shearn et al., 1971)

Name Synonyms

Secondary FlyBase IDs

References (11)

Report Sections

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