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中文
在15号染色体的v38位点，由ENU诱导的A到C的转换，对应于GenBank序列NC_000081中的第6,839个碱基，或者说是NM_009008 mRNA序列的第78,565,945位，这个变异导致了精氨酸(Residue 332)被替换为异亮氨酸(Aspartic Acid to Alanine，D65A)。(来源：J:231801)
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
