Cacna1stm1.1Ics
Targeted Allele Detail
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| 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
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| Alliance: |
Cacna1stm1.1Ics page
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| Germline Transmission: |
Earliest citation of germline transmission:
J:252980
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| Parent Cell Line: |
Not Specified (ES Cell)
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| Strain of Origin: |
C57BL/6NTac
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| Allele Type: |
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Targeted (Not Applicable) |
| Mutations: |
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Insertion, Single point mutation
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Mutation details: A 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)
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| 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
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| Carrying any Cacna1s Mutation: |
117 strains or lines available
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| 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) |
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