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irdc
Spontaneous Allele Detail
Summary
Symbol: irdc
Name: ICR derived retinal dysfunction cone
MGI ID: MGI:3707707
Gene: irdc  Location: unknown  
Alliance: irdc page
Mutation
origin
Strain of Origin:  ICR
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
 
Mutation detailsThis mutation, which is carried together with Gnat1irdr in the IDR1 strain, affects retinal cone physiology.
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any irdc Mutation:  0 strains or lines available
Notes
Mice homozygous for this mutation have impaired cone electrophysiology but normal retinal morphology.
References
Original:  J:119862 Miyamoto M, et al., Visual electrophysiological features of two naturally occurring mouse models with retinal dysfunction. Curr Eye Res. 2006 Apr;31(4):329-35
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory