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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Scnm1m1R
mutation 1, Oak Ridge
MGI:3818057
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Scnm1m1R/Scnm1m1R involves: C57BL/6 MGI:3818071
cx2
Scn8amed-J/Scn8amed-J
Scnm1m1R/Scnm1m1R
involves: C57BL/6 * STOCK Krt71Ca MGI:3818070


Genotype
MGI:3818071
hm1
Allelic
Composition
Scnm1m1R/Scnm1m1R
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scnm1m1R mutation (0 available); any Scnm1 mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• mice are viable

reproductive system
N
• mice are fertile




Genotype
MGI:3818070
cx2
Allelic
Composition
Scn8amed-J/Scn8amed-J
Scnm1m1R/Scnm1m1R
Genetic
Background
involves: C57BL/6 * STOCK Krt71Ca
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scn8amed-J mutation (2 available); any Scn8a mutation (99 available)
Scnm1m1R mutation (0 available); any Scnm1 mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice do not survive beyond weaning

behavior/neurological
N
• unlike Scn8amed-J Scnm1s double homozygotes, mice do not exhibit hindlimb paralysis





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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
11/12/2024
MGI 6.24
The Jackson Laboratory