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Cpfl2
Spontaneous Allele Detail
Summary
Symbol: Cpfl2
Name: cone photoreceptor function loss 2
MGI ID: MGI:3624359
Gene: Cpfl2  Location: unknown  Genetic Position: Chr3, Syntenic
Alliance: Cpfl2 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 Cpfl2 Mutation:  0 strains or lines available
References
Original:  J:167195 Hawes NL, et al., New Mouse Model of Cone Photoreceptor Function Loss (Cpfl2). Invest Ophthalmol Vis Sci. 2003;44(13):4531
All:  3 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
04/09/2024
MGI 6.23
The Jackson Laboratory