Allele Dmel\gl3
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\gl3 | Species | D. melanogaster |
| Name | FlyBase ID | FBal0005042 | |
| Feature type | allele | Created / Updated | 2006-08-22/2006-08-22 |
| Associated gene | Dmel\gl | ||
| Allele class | |||
| Mutagen | spontaneous | ||
Nature of the Allele
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| Allele class | |||
| Mutagen | |||
| Mapped Features and Mutations | |||
Type Symbol & Location Additional Notes References | |||
| Associated Sequence Data | |||
| DDBJ
/
EMBL / GenBank | DNA sequence Protein sequence Name | ||
| UniProtKB/Swiss-Prot | |||
| UniProtKB/TrEMBL | |||
| Progenitor genotype | |||
| Nature of the lesion | Statement Reference Insertion of about 2.5kb of unknown DNA into the gl locus. Insertion of about 2.5kb of unknown DNA (maybe a transposable element). | ||
| Assay mode | |||
| Carried on aberration | |||
| Cytology | |||
Phenotypic Data
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Phenotypic Class
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Phenotype Manifest In
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photoreceptor cell & pupa | |||
Detailed Description
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Statement Reference Weak allele. Eyes small and elliptical with surface less rough than gl1 or gl2. Eye colour: homogeneous scarlet. Ocellus colour: colourless. RK1. Malpighian tubule colour: wild-type. Adult eye is rough, reduced and has a glassy texture. Irregular ommatidia pattern, no rhabdomeres and masses of pigment granules. Photoreceptor cells degenerate and die in the mid-pupal stage at the time when they would normally be producing rhabdomeres (FBrf0074259). Weak allele. The eye is disorganised. Corneal hairs and red pigment granules are only present in the centre of the eye. The ocellar lenses are normal in size, but lack the bulge of the wild-type, and have small protuberances. There are no ocellar retinula cells. The lenses of the compound eye and ocelli are roughened with "corneal nipples". Displays locomotor activity rhythm with an approximately 24h period. Intermediate eye phenotype. | |||
Interactions
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Phenotypic Class
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NOT Enhancer of | |||
Statement Reference | |||
Suppressor of | |||
Statement Reference | |||
NOT Suppressor of | |||
Statement Reference | |||
Phenotype Manifest In
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Enhanced by | |||
Statement Reference gl3 has phenotype, enhanceable by E(gl)2ASC1 gl3 has phenotype, enhanceable by E(gl)2BSC1 gl3 has phenotype, enhanceable by E(gl)2CSC1 gl3 has phenotype, enhanceable by E(gl)2DSC1 gl3 has phenotype, enhanceable by E(gl)2ESC1 gl3 has phenotype, enhanceable by E(gl)2FSC1 gl3 has phenotype, enhanceable by E(gl)2HSC1 gl3 has phenotype, enhanceable by E(gl)3ASC1 gl3 has phenotype, enhanceable by E(gl)3BSCG1 gl3 has phenotype, enhanceable by E(gl)3CSCG1 gl3 has phenotype, enhanceable by E(gl)3DSC1 gl3 has phenotype, enhanceable by E(gl)3DSCG1 gl3 has phenotype, enhanceable by Df(3R)rn20 | |||
NOT Enhancer of | |||
Statement Reference | |||
Suppressor of | |||
Statement Reference | |||
NOT Suppressor of | |||
Statement Reference | |||
Additional Comments
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Genetic Interactions
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Statement Reference | |||
Xenogenetic Interactions
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Statement Reference | |||
Complementation & Rescue Data
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| Fails to complement | |||
| Comments | |||
Stocks
( 21 ) | |||
| Bloomington | 508 | ||
| Kyoto | 105948 | ||
Notes on Origin
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| Discoverer | Stern. | ||
Comments
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Weak gl allele. In a screen for dominant suppressors of hh, 25 out of 84 mutations recovered were at hh. No interaction with P{sev-svp1} or P{sev-svp2} exists. Weak gl mutation. | |||
Synonyms & Secondary IDs
( 4 ) | |||
| Reported As | |||
| Symbol Synonym | gl3 glass3 rh | ||
| Name Synonym | rauhig | ||
| Secondary FlyBase IDs | |||
References
( 20 ) | |||
| Research paper |
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| Book |
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Nature of the Allele