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中文
在11号染色体的v38位置（基对23,757,010），由ENU诱导的C到T的转换，或者在GenBank的NC_000077基因组区域的第13,961位。这个变异对应于NM_009044 mRNA序列中第3个外显子的第472位氨基酸（R472I）。
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
