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中文
在参考序列NM_010635的第1064位(A-T)转换为T-A(替换)，导致编码蛋白质的第339位的谷氨酸(Glu)变为天冬氨酸(Asp)，这在一个必需的锌指结构的第二域(第二锌手指)内，参与DNA结合(来自J:163685)。
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
