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Syne2cpfl8-2J
Spontaneous Allele Detail
Summary
Symbol: Syne2cpfl8-2J
Name: spectrin repeat containing, nuclear envelope 2; cone photoreceptor function loss 8, 2 Jackson
MGI ID: MGI:6358246
Gene: Syne2  Location: Chr12:75865092-76157702 bp, + strand  Genetic Position: Chr12, 33.11 cM
Alliance: Syne2cpfl8-2J page
Mutation
origin
Strain of Origin:  B6;129-Cacna1htm1Kcam/J
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Undefined
    This spontaneous mutation was proven to be allelic by failed complementation with the cpfl8 allele. (J:278495)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 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 Syne2 Mutation:  297 strains or lines available
References
Original:  J:278495 Chang B, Three cone photoreceptor function loss mutations in the Syne2 gene. MGI Direct Data Submission. 2019;
All:  1 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
03/19/2024
MGI 6.23
The Jackson Laboratory