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Scn8aM1Btlr
Chemically induced Allele Detail
Summary
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
Alliance: Scn8aM1Btlr page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Beutler Mutagenetix
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThis 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)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Scn8a Mutation:  99 strains or lines available
References
Original:  J:139714 Timms H, et al., Record for "TremorD" updated October 7th, 2008. MGI Direct Data Submission. 2008;
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
12/10/2024
MGI 6.24
The Jackson Laboratory