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Cacna1stm1.1Ics
Targeted Allele Detail
Summary
Symbol: Cacna1stm1.1Ics
Name: calcium channel, voltage-dependent, L type, alpha 1S subunit; targeted mutation 1.1, Mouse Clinical Institute
MGI ID: MGI:6781961
Synonyms: ncDHPR
Gene: Cacna1s  Location: Chr1:135980549-136047268 bp, + strand  Genetic Position: Chr1, 59.55 cM, cytoband F
Alliance: Cacna1stm1.1Ics page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:252980
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  C57BL/6NTac
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutations:    Insertion, Single point mutation
 
Mutation detailsA mutation was engineered in exon 13 to change asparagine codon 617 (AAC) to an aspartic acid codon (GAC)(p.N617D) and a loxP site, an FRT site flanked protamine-cre cassette, a neomycin resistance gene cassette and a second loxP site were inserted in opposite transcriptional orientation into intron 12. The floxed cre plus neo cassette pair was self-excised in male germline through the protamine promotor-driven expression of Cre. The mutation in this allele creates a non-Ca2+-conducting form of the encoded peptide. (J:252980)
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 Cacna1s Mutation:  117 strains or lines available
References
Original:  J:252980 Dayal A, et al., The Ca2+ influx through the mammalian skeletal muscle dihydropyridine receptor is irrelevant for muscle performance. Nat Commun. 2017 Sep 07;8(1):475
All:  4 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
12/30/2025
MGI 6.24
The Jackson Laboratory