All Phenotypes Scnm1<m1R> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Scnm1^m1R
mutation 1, Oak Ridge
MGI:3818057

Summary

2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Scnm1^m1R/Scnm1^m1R	involves: C57BL/6	MGI:3818071
cx2	Scn8a^med-J/Scn8a^med-J Scnm1^m1R/Scnm1^m1R	involves: C57BL/6 * STOCK Krt71^Ca	MGI:3818070

Allelic Composition	Scnm1^m1R/Scnm1^m1R
Genetic Background	involves: C57BL/6

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scnm1^m1R mutation (0 available); any Scnm1 mutation (17 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

mortality/aging ( J:141236 )

N	• mice are viable

reproductive system

reproductive system phenotype ( J:141236 )

N	• mice are fertile

Allelic Composition	Scn8a^med-J/Scn8a^med-J Scnm1^m1R/Scnm1^m1R
Genetic Background	involves: C57BL/6 * STOCK Krt71^Ca

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scn8a^med-J mutation (2 available); any Scn8a mutation (99 available)
Scnm1^m1R mutation (0 available); any Scnm1 mutation (17 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

postnatal lethality ( J:141236 )

• mice do not survive beyond weaning

behavior/neurological

behavior/neurological phenotype ( J:141236 )

N	• unlike Scn8a^med-J Scnm1^s double homozygotes, mice do not exhibit hindlimb paralysis

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