FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\L2
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General Information
Symbol
Dmel\L2
Species
D. melanogaster
Name
FlyBase ID
FBal0005882
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Mutagen
Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description

roo element inserted in the 3' intergenic region downstream of L. This roo{}L-2 insertion contains a number of sequence alterations (622bp duplication, 5bp deletion, a nucleotide change that results in the formation of an ATG) compared to roo{}Mohr (an insertion found in a number of dominant L mutant alleles isolated around 1920, and also in the ft1 chromosome isolated during the same time period), and probably arose by alteration of it. Reversion analysis suggests that the roo{}L-2 insertion is largely responsible for the dominant L2 eye phenotype. The chromosome also carries a number of other natural transposon insertions in the L region (jockey{}Mohr and opus{}Mohr), however these insertions are found in a number of dominant L mutant alleles isolated around 1920, and also in the ft1 chromosome isolated during the same time period, suggesting that the additional insertions are probably not related to the dominant L mutant eye phenotype.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
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
Detailed Description
Statement
Reference

L2 heterozygotes exhibit a selective loss of ventral eye in the larval eye imaginal disc and adult eye.

L2/+ flies show a loss of the ventral eye cells both at the eye disc and adult eye level. Use of the TUNEL assay reveals that cell death occurs predominantly in the ventral eye margin of the L2/+ eye disc but not in the dorsal half of the eye.

Heterozygotes show loss of almost all ventral ommatidia; apart from a few cells along the ventral eye margin, nearly all ommatidia in L2/+ flies are dorsal in fate. This loss of ventral eye pattern is also seen in heterozygous eye discs.

Heterozygotes have a nick near the anterior midline of the eye and the overall size of the eye is reduced.

L2 flies do not differ from wild type in speed of development.

Eyes of L2/+ as small as or smaller than L1/L1. L2 homozygotes have tiny eyes and are poorly viable or completely lethal, depending on background.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement
Reference

L2 has visible | dominant phenotype, enhanceable by +/Df(2L)BSC7

L2 has visible | dominant phenotype, enhanceable by emcEP415/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, enhanceable by esg05729/esg[+]

L2 has visible | dominant phenotype, enhanceable by hhbar3/hhbar3

L2 has visible | dominant phenotype, enhanceable by sgg[+]/sgg1

L2 has visible | dominant phenotype, enhanceable by aopEP598/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, enhanceable by B[+]/Bar1

NOT Enhanced by
Statement
Reference

L2 has visible | dominant phenotype, non-enhanceable by PRAS40[+]/PRAS40P17

L2 has visible | dominant phenotype, non-enhanceable by PRAS40[+]/PRAS40KO

L2 has visible | dominant phenotype, non-enhanceable by phylJF03369/Scer\GAL4ey.PU

L2 has visible | dominant phenotype, non-enhanceable by phylGD12579/Scer\GAL4ey.PU

L2 has visible | dominant phenotype, non-enhanceable by Scer\GAL4ey.PU/AchlJF01976

Suppressed by
Statement
Reference

L2 has visible | dominant | adult stage phenotype, suppressible by hyxEY06898

L2 has visible | dominant phenotype, suppressible by pygounspecified

L2 has visible | dominant phenotype, suppressible by CBPEP1643/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by Df(1)Bar/+

L2 has visible | dominant phenotype, suppressible by Df(3L)iro-DFM3

L2 has visible | dominant phenotype, suppressible by dcoEP3280/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by emc[+]/emc12

L2 has visible | dominant phenotype, suppressible by esgEP2159/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by esgEP2408/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by esgEP633/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by esgEP683/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by fngEP3082/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by hhEP3521/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by Scer\GAL4ey.PH/kek1EP655

L2 has visible | dominant phenotype, suppressible by nocEP2173/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by pnr[+]/pnrVX6

L2 has visible | dominant phenotype, suppressible by rasEP1235/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by rasEP1427/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by smoEP1220/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by wunEP2208/Scer\GAL4ey.PH

L2 has visible | dominant phenotype, suppressible by sggEP1576/Scer\GAL4ey.PH

NOT suppressed by
Statement
Reference

L2 has visible | dominant phenotype, non-suppressible by PRAS40[+]/PRAS40P17

L2 has visible | dominant phenotype, non-suppressible by PRAS40[+]/PRAS40KO

L2 has visible | dominant phenotype, non-suppressible by phylJF03369/Scer\GAL4ey.PU

L2 has visible | dominant phenotype, non-suppressible by phylGD12579/Scer\GAL4ey.PU

L2 has visible | dominant phenotype, non-suppressible by Scer\GAL4ey.PU/AchlJF01976

Enhancer of
Statement
Reference

L2/L[+] is an enhancer of visible phenotype of Scer\GAL4ey.PH, pnrD4.UAS

L2/L[+] is an enhancer of visible phenotype of Scer\GAL4bi-omb-Gal4, pnrD4.UAS

Other
Phenotype Manifest In
Enhanced by
Statement
Reference

L2 has eye | somatic clone phenotype, enhanceable by hth[+]/hth100-1

L2 has eye disc | somatic clone phenotype, enhanceable by hth[+]/hth100-1

L2 has eye | somatic clone phenotype, enhanceable by hth[+]/hthMeis1-P2

L2 has eye disc | somatic clone phenotype, enhanceable by hth[+]/hthMeis1-P2

L2 has eye | ventral phenotype, enhanceable by Scer\GAL4ey.PH/wgUAS.cAa

L2 has eye | ventral phenotype, enhanceable by bskUAS.cBa/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, enhanceable by JraAsp.B.UAS/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, enhanceable by armUAS.cUa/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by rodEP3408/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by +/Df(2L)BSC7

L2 has eye phenotype, enhanceable by Scer\GAL4ey.PH/EP1350EP1350

L2 has eye phenotype, enhanceable by Scer\GAL4ey.PH/EP1410EP1410

L2 has eye phenotype, enhanceable by EP3087EP3087/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by EP950EP950/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by araUAS.cGa/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by Scer\GAL4ey.PH/dallyEP3168

L2 has eye phenotype, enhanceable by emcEP3166/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by emcEP3614/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by emcEP3620/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by DadEP3196/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by emcEP415/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by esg05729/esg[+]

L2 has eye phenotype, enhanceable by hhbar3/hhbar3

L2 has eye phenotype, enhanceable by Scer\GAL4ey.PH/mirrUAS.cMa

L2 has eye phenotype, enhanceable by nejEP1149/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by Scer\GAL4ey.PH/nejEP1179

L2 has eye phenotype, enhanceable by sgg[+]/sgg1

L2 has eye phenotype, enhanceable by aopEP2500/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by aopEP598/Scer\GAL4ey.PH

L2 has eye phenotype, enhanceable by B[+]/Bar1

NOT Enhanced by
Statement
Reference

L2 has eye phenotype, non-enhanceable by PRAS40[+]/PRAS40P17

L2 has eye phenotype, non-enhanceable by PRAS40[+]/PRAS40KO

L2 has eye phenotype, non-enhanceable by PRAS40RNAi.WIZ.UAS/Scer\GAL4ey.PU

L2 has eye phenotype, non-enhanceable by phylJF03369/Scer\GAL4ey.PU

L2 has eye phenotype, non-enhanceable by phylGD12579/Scer\GAL4ey.PU

L2 has eye phenotype, non-enhanceable by Scer\GAL4ey.PU/AchlJF01976

L2 has eye disc | somatic clone phenotype, non-enhanceable by exd[+]/exd1

L2 has eye | somatic clone phenotype, non-enhanceable by exd[+]/exd1

L2 has eye | somatic clone phenotype, non-enhanceable by exdUAS.cGa/Scer\GAL4ey.PH

L2 has eye disc | ventral phenotype, non-enhanceable by p53UAS.Ex/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, non-enhanceable by p53UAS.Ex/Scer\GAL4ey.PH

Suppressed by
Statement
Reference

L2 has eye | somatic clone phenotype, suppressible by hthdtl-S142204/hth[+]

L2 has eye disc | somatic clone phenotype, suppressible by hthdtl-S142204/hth[+]

L2 has eye phenotype, suppressible by hth1-430.EnR.UAS/Scer\GAL4ey.PH

L2 has eye phenotype, suppressible by hyxEY06898

L2 has eye | ventral phenotype, suppressible by Diap1UAS.cLa/Scer\GAL4ey.PH

L2 has eye disc | ventral phenotype, suppressible by Df(3L)H99/+

L2 has eye | ventral phenotype, suppressible by Df(3L)H99/+

L2 has eye | ventral phenotype, suppressible by Scer\GAL4ey.PH/sggS9A.UAS

L2 has eye | ventral phenotype, suppressible by panΔN.UAS/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by wg1

L2 has eye disc | ventral phenotype, suppressible by wg1

L2 has eye | ventral phenotype, suppressible by pucUAS.cMa/Scer\GAL4ey.PH

L2 has eye disc | ventral phenotype, suppressible by bskDN.UAS/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by bskDN.UAS/Scer\GAL4ey.PH

L2 has eye disc | ventral phenotype, suppressible by hep[+]/hepr75

L2 has eye | ventral phenotype, suppressible by hep[+]/hepr75

L2 has eye | ventral phenotype, suppressible by pygounspecified

L2 has eye | ventral phenotype, suppressible by ushUAS.cFa/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by CBPEP1643/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by CG12054EP3309/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by GstE12EP2452/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by CG42709EP3622/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by CG3308EP1230/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by Scer\GAL4ey.PH/Hmt-1EP3387

L2 has eye | ventral phenotype, suppressible by Scer\GAL4ey.PH/CG7920EP3096

L2 has eye | ventral phenotype, suppressible by Df(1)Bar/+

L2 has eye | ventral phenotype, suppressible by Df(3L)iro-DFM3

L2 has eye | ventral phenotype, suppressible by mir-278EP1229/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by Scer\GAL4ey.PH/EP1324EP1324

L2 has eye | ventral phenotype, suppressible by EP2012EP2012/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by EP2031EP2031/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by Scer\GAL4ey.PH/EP2370EP2370

L2 has eye | ventral phenotype, suppressible by EP3123EP3123/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by NFATEP1353/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by NFATEP1508/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by TfIIA-SEP3285/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by Cul4EP2518/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by dcoEP3280/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by emc[+]/emc12

L2 has eye | ventral phenotype, suppressible by esgEP2159/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by esgEP2408/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by esgEP633/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by esgEP683/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by fngEP3082/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by hhEP3521/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by Scer\GAL4ey.PH/kek1EP655

L2 has eye | ventral phenotype, suppressible by nocEP2173/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by nrv1EP2454/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by pnr[+]/pnrVX6

L2 has eye | ventral phenotype, suppressible by rasEP1235/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by rasEP1427/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by sggEP1576/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by smoEP1220/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, suppressible by wunEP2208/Scer\GAL4ey.PH

NOT suppressed by
Statement
Reference

L2 has eye phenotype, non-suppressible by PRAS40[+]/PRAS40KO

L2 has eye phenotype, non-suppressible by PRAS40RNAi.WIZ.UAS/Scer\GAL4ey.PU

L2 has eye phenotype, non-suppressible by phylJF03369/Scer\GAL4ey.PU

L2 has eye phenotype, non-suppressible by phylGD12579/Scer\GAL4ey.PU

L2 has eye phenotype, non-suppressible by Scer\GAL4ey.PU/AchlJF01976

L2 has eye phenotype, non-suppressible by PRAS40[+]/PRAS40P17

L2 has eye disc | somatic clone phenotype, non-suppressible by exd[+]/exd1

L2 has eye | somatic clone phenotype, non-suppressible by exd[+]/exd1

L2 has eye | somatic clone phenotype, non-suppressible by exdUAS.cGa/Scer\GAL4ey.PH

L2 has eye disc | ventral phenotype, non-suppressible by p53259H.GUS/Scer\GAL4ey.PH

L2 has eye | ventral phenotype, non-suppressible by p53259H.GUS/Scer\GAL4ey.PH

L2 has eye disc | ventral | first instar larval stage phenotype, non-suppressible by wgl-12

L2 has eye disc | ventral | third instar larval stage phenotype, non-suppressible by wgl-12

Enhancer of
Statement
Reference

L2/L[+] is an enhancer of eye phenotype of Scer\GAL4ey.PH, wgUAS.cAa

L2/L[+] is an enhancer of eye disc phenotype of Scer\GAL4ey.PH, wgUAS.cAa

L2/L[+] is an enhancer of eye phenotype of bskUAS.cBa

L2/L[+] is an enhancer of eye phenotype of Scer\GAL4ey.PH, armUAS.cUa

L2/L[+] is an enhancer of eye disc phenotype of Scer\GAL4ey.PH, armUAS.cUa

L2/L[+] is an enhancer of eye phenotype of Scer\GAL4ey.PH, pnrD4.UAS

L2/L[+] is an enhancer of eye phenotype of Scer\GAL4bi-omb-Gal4, pnrD4.UAS

Other
Additional Comments
Genetic Interactions
Statement
Reference

Increasing levels of hth in L2 heterozygotes through expression of hthScer\UAS.cPa under the control of Scer\GAL4ey.PH enhances the ventral eye loss to a 'no eye' phenotype. This loss of eye fate is due to an eye-to-cuticle fate change. There is no effect on the antennal field.

A hthdtl-S142204 heterozygous background partially suppresses the loss-of-ventral eye phenotype found in L2/+ mutants.

Loss-of-function L2 heterozygous eye clones in a hth100-1 or hthMeis1-P2 heterozygous background results in a complete loss-of-ventral eye phenotype, as seen in L2 eye clones.

exd1/+; L2/+ double heterozygous mutants exhibit the same loss-of-ventral-eye phenotype as L2/+ mutants.

Over-expression of exdScer\UAS.cGa under the control of Scer\GAL4ey.PH in a L2 heterozygous background does not affect the loss-of-ventral-eye phenotype found in L2/+ mutants.

Expression of p53Scer\UAS.Ex under the control of Scer\GAL4ey.PH does not enhance the L2/+ mutant phenotype of ventral eye loss. Further, expression of the dominant negative p53259H.GUS transgene, under the control of Scer\GAL4ey.PH, does not suppress the L2/+ phenotype.

Expression of Diap1Scer\UAS.cLa under the control of Scer\GAL4ey.PH results in a partial suppression of the L2/+ phenotype. 27% of rescued flies have eyes that are more than three-quarters of the wild-type size and a range of intermediate and weaker rescues are observable in the other 73%.

L2/+; Df(3L)H99/+ flies show an almost complete rescue of the L2/+ phenotype in 38% of adult flies.

The L2/+ loss-of-ventral eye phenotype can be rescued by reducing canonical wg signaling components. The ventral eye is restored in L2, wg1/+ double mutants, in which ommatidia in the restored ventral section show correct ventral eye polarity. The temperature sensitive wgl-12 allele can only significantly rescue the L2 ventral eye loss phenotype when larvae are shifted to the restrictive temperature during the second larval instar; shifting to the restrictive temperature during the first or third instar has no effect on the L2 phenotype. Expression of sggS9A.Scer\UAS under the control of Scer\GAL4ey.PH provides a partial rescue of the ventral eye loss phenotype of L2/+ flies; the suppression is significant in 26% of flies and is weak in the remaining flies, while expression of panΔN.Scer\UAS under the control of Scer\GAL4ey.PH significantly rescues the ventral eye loss of L2/+ flies in 23% of cases.

Increasing wg signaling leads to an enhancement of the L2/+ loss-of-ventral eye phenotype. Expression of either wgScer\UAS.cAa or armScer\UAS.cUa, under the control of Scer\GAL4ey.PH, in L2/+ mutants results in a no eye phenotype, while small eyes are observed in all of the single mutants. Expression of dshScer\UAS.T:Hsap\MYC under the control of Scer\GAL4ey.PH leads to an enhancement of the ventral eye loss.

Blocking JNK signaling significantly represses the L2/+ loss-of-ventral eye phenotype. Expression of pucScer\UAS.cMa (a JNK down-regulator) under the control of Scer\GAL4ey.PH results in rescue of the ventral eye loss of L2/+ mutants in 36% of cases. Expression of the dominant negative bskDN.Scer\UAS under the control of Scer\GAL4ey.PH results in rescue of the ventral eye loss of L2/+ mutants in 36% of cases, while 32% of hepr75/+; L2/+ flies show a strong suppression of the ventral eye loss phenotype seen in L2/+ flies. In contrast, increasing JNK signaling enhances the phenotype; expression of bskScer\UAS.cBa under the control of Scer\GAL4ey.PH enhances the loss-of-ventral-eye phenotype to near complete loss in 39% of L2/+ flies, while expression of JraAsp.B.Scer\UAS under the control of Scer\GAL4ey.PH results in a strong enhancement of the L2/+ eye phenotype to a very small eye or no eye in 36% of flies.

*j Free text: Expression of BacA\p35Scer\UAS.cHa under the control of Scer\GAL4ey.PH results in a partial suppression of the ventral eye loss in L2/+ flies; 40% of rescued flies have ventral eyes that are more than three-quarters of the wild-type size. The remaining 60% of rescued flies show a range of weaker phenotypes than L2/+ eyes.

Coexpression of BacA\p35Scer\UAS.cHa and pucScer\UAS.cMa under the control of Scer\GAL4ey.PH rescues the ventral eye loss of L2/+ flies to a near wild-type eye in 69% of flies and pharate adults; this is a much greater suppression than that seen when either transgene is expressed without the other.

sgg1/+ ; L2/+ flies show complete elimination of the eye field in 15% of cases. L2/+ ; hhbar3/hhbar3 and L2/Df(2L)BSC7 flies show complete elimination of the eye. L2/+ pharate adults expressing EP1350EP1350 under the control of Scer\GAL4ey.PH have a no eye phenotype, but the antennal field is not affected. B1/+ ; L2/+ animals have a no eye phenotype. Only 41% of L2/+ animals expressing pnrD4.Scer\UAS under the control of Scer\GAL4ey.PH eclose, and these animals have greatly reduced heads with no eyes, but normal antennae. Only 41% of L2/+ animals expressing pnrD4.Scer\UAS under the control of Scer\GAL4ey.PH eclose, and these animals have greatly reduced heads with no eyes, but normal antennae. L2/+ increases the frequency of the no-eye phenotype seen in discs of animals expressing ushScer\UAS.cFa under the control of Scer\GAL4ey.PH at 29oC throughout development from 80% to nearly 98% and the animals fail to eclose. The L2/+ phenotype of ventral eye loss is unaffected if expression of ushScer\UAS.cFa is driven by Scer\GAL4ey.PH at 29oC from embryogenesis until the end of the first larval instar, or by Scer\GAL4ey.PH at 29oC from during the third larval instar. However, if ushScer\UAS.cFa expression is driven by Scer\GAL4ey.PH at 29oC during the second larval instar, the L2/+ ventral eye phenotype is significantly rescued.

Xenogenetic Interactions
Statement
Reference

Misexpression of en::hthR.1-430.Scer\UAS in L2 under the control of Scer\GAL4ey.PH mutants causes a significant suppression of the loss-of-ventral eye phenotype in the larval eye imaginal disc and the adult eye.

Expression of BacA\p35Scer\UAS.cHa under the control of Scer\GAL4ey.PH results in a partial suppression of the ventral eye loss in L2/+ flies; 40% of rescued flies have ventral eyes that are more than three-quarters of the wild-type size. The remaining 60% of rescued flies show a range of weaker phenotypes than L2/+ eyes.

Coexpression of BacA\p35Scer\UAS.cHa and pucScer\UAS.cMa under the control of Scer\GAL4ey.PH rescues the ventral eye loss of L2/+ flies to a near wild-type eye in 69% of flies and pharate adults; this is a much greater suppression than that seen when either transgene is expressed without the other.

Complementation and Rescue Data
Rescued by
Partially rescued by

L2/L[+] is partially rescued by LJF01943/Scer\GAL4ey.PU

L2/L[+] is partially rescued by Scer\GAL4ey.PU/LKK102438

Comments

Expression of either LKK102438 or LJF01943 under the control of Scer\GAL4ey.PU partially suppresses the L2/+ eye phenotype.

Images (0)
Mutant
Wild-type
Stocks (24)
Notes on Origin
Discoverer

Mohr, 2nd Feb. 1920.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
References (16)