Scn8aM1Btlr
Chemically induced Allele Detail
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Symbol: |
Scn8aM1Btlr |
Name: |
sodium channel, voltage-gated, type VIII, alpha; mutation 1, Bruce Beutler |
MGI ID: |
MGI:3809770 |
Synonyms: |
TremorD |
Gene: |
Scn8a Location: Chr15:100767739-100943819 bp, + strand Genetic Position: Chr15, 56.39 cM, cytoband F1
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Alliance: |
Scn8aM1Btlr page
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Strain of Origin: |
C57BL/6J
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Project Collection: |
Beutler Mutagenetix
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Allele Type: |
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Chemically induced (ENU) |
Mutation: |
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Single point mutation
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Mutation details: This mutation was identified by its behavioral phenotype among G3 progeny of an ENU mutagenized male mouse. It was mapped to Chr 15 and found to correspond to a G to T transversion at nucleotide position 2919 of the gene (Genbank: NM_001077499). This is predicted to result in replacement of tryptophan by leucine at amino acid position 935 (W935L), which resides in the pore loop between helices S5 and S6 of domain II.
(J:139714)
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Inheritance: |
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Semidominant |
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View phenotypes and curated references for all genotypes (concatenated display).
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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 Scn8a Mutation: |
99 strains or lines available
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Original: |
J:139714 Timms H, et al., Record for "TremorD" updated October 7th, 2008. MGI Direct Data Submission. 2008; |
All: |
1 reference(s) |
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