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cpfl6
Spontaneous Allele Detail
Summary
Symbol: cpfl6
Name: cone photoreceptor function loss 6
MGI ID: MGI:4867510
Gene: cpfl6  Location: unknown  Genetic Position: Chr13, Syntenic
Alliance: cpfl6 page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Spontaneous
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 cpfl6 Mutation:  0 strains or lines available
References
Original:  J:167198 Chang B, et al., A New Mouse Model of Cone Photoreceptor Function Loss (cpfl6) Associated With the Targeted Hcn1 Gene Mutation. Invest Ophthalmol Vis Sci. 2006;47(13):2294
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