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中文
在16号染色体的v38位置（15,719,433基对），由ENU诱导的T到C的转换，或者在GenBank的NC_000082基因组区域的第81,991位。这个变异对应于NM_011159 mRNA序列中第39个外显子的第5,170位氨基酸（V1716A）。(来源：J:255268)
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
