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中文
dmu小鼠和Scn8amed小鼠的基因补全测试结果显示，这两种突变是等位基因。该基因的转录水平在纯合子小鼠中显著降低。该突变体在GenBankNM_011323的exon 10A位置1538处有一个单核苷酸缺失。(来源：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
