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中文
在7号染色体的v38位置，由ENU诱导的A到T的转换，具体位置是5,629,5498 base pair(或NC_000073基因组区域的55,906号位置)。这个变异等同于NM_021879 mRNA序列中第285位的氨基酸，位于第8个外显子的24个总外显子中。该突变导致了Arginine(285)被替换为一个早终止密码子(R285*)。参考文献：J:255212
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
