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中文
这种突变是在一个基于ENU的前向遗传筛选中发现的，它导致了在不变的exon 7上发生C到T的变异，产生了一个在第三外分泌免疫球蛋白样域中第263位有错义突变（Pro263Ser）的多肽。这通常会被认为是隐性突变的等位基因。(来源：J:216825)
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
