FB2024_03 , released June 25, 2024
Allele: Dmel\rin1
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General Information
Symbol
Dmel\rin1
Species
D. melanogaster
Name
FlyBase ID
FBal0117391
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
P4957
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

P{lacW} insertion in an alternative exon in the 5' UTR.

Allele components
Component
Use(s)
Inserted element
Encoded product / tool
Mutations Mapped to the Genome
Curation Data
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

Hemizygous rin[1]/Df(3R)urd flies emerge at a lower than expected frequency compared to their heterozygous siblings.

Homozygous rin1 flies have normal lifespan.

Homozygotes and rin1/rin2 flies are viable and show a mild rough eye phenotype. Homozygous eyes show defects in both photoreceptor recruitment and ommatidial polarity. Many ommatidia have fewer than the wild-type complement of 8 photoreceptors and some have extra photoreceptors. Both inner and outer photoreceptors can be affected. Many mutant ommatidia with the normal complement of photoreceptors show polarity defects; both the degree and direction of rotation and the chirality of the ommatidia can be affected. The recruitment and polarity defects are evident in third larval instar imaginal discs.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressor of
Statement
Reference

rin1/rin[+] is a suppressor of visible phenotype of Ras85DV12.sev

rin1/rin[+] is a suppressor of visible phenotype of svp2.sev

Phenotype Manifest In
Enhancer of
Statement
Reference

rin1/rin[+] is an enhancer of photoreceptor cell R7 phenotype of SosJC2, sev6

NOT Enhancer of
Statement
Reference

rin1 is a non-enhancer of phenotype of RasGAP11-16

rin1 is a non-enhancer of phenotype of RasGAP1UAS.cGa, Scer\GAL4hs.2sev

Suppressor of
Statement
Reference

rin1/rin[+] is a suppressor of eye phenotype of svp2.sev

rin1/rin[+] is a suppressor of eye phenotype of Ras85DV12.sev

rin1/rin[+] is a suppressor of phenotype of sevS11.Tag:MYC

rin1/rin[+] is a suppressor of ommatidium phenotype of sevS11.Tag:MYC

rin1/rin[+] is a suppressor of photoreceptor cell R7 | ectopic phenotype of sevS11.Tag:MYC

NOT Suppressor of
Statement
Reference

rin1 is a non-suppressor of phenotype of RasGAP11-16

rin1 is a non-suppressor of phenotype of RasGAP1UAS.cGa, Scer\GAL4hs.2sev

rin1 is a non-suppressor of phenotype of Raf::tor12D.sev

rin1 is a non-suppressor of phenotype of rlSem

Additional Comments
Genetic Interactions
Statement
Reference

The extra R7 photoreceptor cells seen in flies carrying sevS11.T:Hsap\MYC are reduced to an average of 2.71 +/- 0.23 R7 photoreceptor cells per ommatidium if the flies are also carrying rin1. 18.7% of ommatidia have an R7 cell in sev6; SosJC2 flies. This partial rescue of sev6 by SosJC2 is relieved by rin1; 13.9% of ommatidia have an R7 cell in sev6; SosJC2/+ ; rin1/+ flies.

28.7% of ommatidia have an R7 cell in sev6 ; SosJC2 flies. This partial rescue of sev6 by SosJC2 is relieved by rin1 or rin2; 13.9% and 18.2% of ommatidia have an R7 cell in sev6 ; SosJC2/+ ; rin1/+ and sev6 ; SosJC2/+ ; rin2/+ flies respectively.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

Selected as: a modifier of the svp2.sev eye phenotype.

Comments
Comments

The rin1 homozygous phenotype and the dominant suppression of the svp2.sev eye phenotype are revertable on excision of the P-element.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (2)