Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Crxtvrm65
Name:	cone-rod homeobox; translational vision research model 65
MGI ID:	MGI:4867395
Synonyms:	Crx-L253X
Gene:	Crx  Location: Chr7:15599872-15613880 bp, - strand  Genetic Position: Chr7, 8.6 cM
Alliance:	Crxtvrm65 page

Strain of Origin:

C57BL/6J

Allele Type:    Chemically induced (ENU) Mutation:    Single point mutation   Mutation details: A T-to-A nonsense mutation in the last exon of the gene is predicted to alter the leucine 277 residue to a termination codon in the encoded protein. This mutation affects both known isofoms. (J:166679)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

5 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Crx Mutation:	26 strains or lines available

Original:	J:166679 Won J, et al., Mouse model resources for vision research. J Ophthalmol. 2011;2011:391384
All:	5 reference(s)