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Opa1Q285X
Chemically induced Allele Detail
Nomenclature
Symbol: Opa1Q285X
Name: optic atrophy 1; Q285X
MGI ID: MGI:3711758
Synonyms: Opa1Q285STOP
Gene: Opa1  Location: Chr16:29579334-29654884 bp, + strand  Genetic Position: Chr16, 20.65 cM, cytoband B2
Mutation
origin
Strain of Origin:  C3HeB/FeJ
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation details
Inheritance:    Not Specified
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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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 Opa1 Mutation:  8 strains or lines available
References
Original:  J:121779 Davies VJ, et al., Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function. Hum Mol Genet. 2007 Jun 1;16(11):1307-18
All:  6 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/15/2014
MGI 5.18
The Jackson Laboratory