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

Symbol:	Cacna1fnob9
Name:	calcium channel, voltage-dependent, alpha 1F subunit; no b wave 9
MGI ID:	MGI:5817401
Gene:	Cacna1f  Location: ChrX:7473342-7501435 bp, + strand  Genetic Position: ChrX, 3.42 cM
Alliance:	Cacna1fnob9 page

Strain of Origin:

C57BL/6J-Chr 10.3PWD/Ph/ForeJ

Allele Type:    Spontaneous (Not Specified) Mutations:    Intragenic deletion, Single point mutation   Mutation details: This spontaneous mutation involves an intronic G-to-A substitution, which creates a novel CAG splice acceptor site. Use of this ectopic acceptor creates a mis-spliced transcript with a 10 bp 5' extension of exon 14 that results in a frameshift and premature stop codon. (J:267160) Inheritance:    Recessive

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

In Structures Affected by this Mutation:

3 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 Cacna1f Mutation:	19 strains or lines available

Original:	J:267160 Dai X, et al., Photoreceptor degeneration in a new Cacna1f mutant mouse model. Exp Eye Res. 2018 Nov 13;179:106-114
All:	1 reference(s)