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中文
这个突变是44,724,449号碱基对上的A到T替换，发生在基因组的Chromosome 4区域，NC_00070（NCBI Ref37版本）。这个位置距离ATG启动子有175个核苷酸，导致了蛋白质表达的丧失。（来源：J:220072）
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
