About   Help   FAQ
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
Loading...
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory