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Genetic complementation testing between the dmu mouse and Scn8amed mice demonstrated that these two mutations are allelic. Transcript levels from this gene are greatly reduced in homozygous mice. This mutant contains a single nucleotide deletion in exon 10A (position 1538 in GenBank NM_011323). (J:98511)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
