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中文
在7号染色体的v38位置，由ENU诱导的G到A的转换，具体位置是12,267,663号碱基对，或者在GenBank的NC_000073基因组区域的338,539号位置。这个变异等同于NM_008855 mRNA序列中第17个外显子的第2,091位氨基酸的替换，即R624Q。(来源：J:274862)
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
