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中文
在5号染色体的v38(88,772,723位点)由ENU诱导的T到C的转换，或者在NC_000071 GenBank中的7,711号碱基位置。这个变异对应于NM_007832 mRNA序列中第3个外显子的第544位氨基酸(544C到544R)的替换。(引用:J:236696)
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
