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Scn10aPsm
Chemically induced Allele Detail
Summary
Symbol: Scn10aPsm
Name: sodium channel, voltage-gated, type X, alpha; possum
MGI ID: MGI:3794859
Synonyms: Nav1.8Possum, Scn10am1Btlr
Gene: Scn10a  Location: Chr9:119437522-119548388 bp, - strand  Genetic Position: Chr9, 71.33 cM, cytoband distal
Alliance: Scn10aPsm page
Scn10aPsm/Scn10aPsm mice display inducible immobility

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsAn A-to-G transition at nucleotide position 2403 of the gene (Genbank Accession NM_009134) results in replacement of threonine by alanine at amino acid position 790 of the Nav1.8 protein. This mutation produces a dominant hypermorph. (J:180381)
Inheritance:    Dominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 Scn10a Mutation:  102 strains or lines available
References
Original:  J:180381 Blasius AL, et al., Hypermorphic mutation of the voltage-gated sodium channel encoding gene Scn10a causes a dramatic stimulus-dependent neurobehavioral phenotype. Proc Natl Acad Sci U S A. 2011 Nov 29;108(48):19413-8
All:  2 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
10/29/2024
MGI 6.24
The Jackson Laboratory