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Scn4am1Aaa
Chemically induced Allele Detail
Summary
Symbol: Scn4am1Aaa
Name: sodium channel, voltage-gated, type IV, alpha; mutation 1, Abraham Acevedo-Arozena
MGI ID: MGI:5308659
Synonyms: Dgn, draggen, Scn4am1H
Gene: Scn4a  Location: Chr11:106209418-106244114 bp, - strand  Genetic Position: Chr11, 68.91 cM
Alliance: Scn4am1Aaa page
Mutation
origin
Strain of Origin:  BALB/cAnN
Mutation
description
Allele Type:    Chemically induced (ENU)
Inheritance:    Dominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 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 Scn4a Mutation:  70 strains or lines available
References
Original:  J:217522 Corrochano S, et al., Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis. Brain. 2014 Dec;137(Pt 12):3171-85
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
04/16/2024
MGI 6.23
The Jackson Laboratory