Symbol
Name
ID
|
|
|
Synonyms
|
3110001I17Rik
|
|
Genetic Map
|
|
|
Sequence Map
|
|
Mammalian homology
|
|
|
Sequences
|
All sequences(16)
|
Alleles and phenotypes
|
All alleles(10) :
Targeted, knock-out(1)
Targeted, other(1)
Gene trapped(6)
Spontaneous(1)
Chemically induced(1)
| The Scnm1 locus influences the severity of the Scn8a phenotype. Mice carrying the recesive susceptibility allele of the modifier are paralyzed and do not survive beyond 1 month. Mice carryimg the resistant wildtype allele display progressive dystonia with ataxia and live more than 1.5 years. |
|
|
Polymorphisms
|
SNPs within 2kb(44 from dbSNP Build 128)
|
Gene Ontology (GO) classifications
|
|
|
Expression
|
cDNA source data(71)
External Resources:
Allen Brain Atlas
GENSAT
GEO
ArrayExpress
|
Molecular reagents
|
All nucleic(71)
cDNA(71)
Microarray probesets(2)
|
Other database links
|
|
|
References
|
(Earliest)
J:53340
Sprunger LK et al.,
"Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3."
Hum Mol Genet 1999 Mar;8(3):471-9
(Latest)
J:141236
Howell VM et al.,
"A Targeted Deleterious Allele of the Splicing Factor SCNM1 in the Mouse."
Genetics 2008 Nov;180(3):1419-27
|
All references(10)
|
Other accession IDs
|
MGI:1916519
|