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中文
在GRCm38染色体15号的6,696,520位碱基(基对)，由ENU诱导的T到A的突变，或者在GenBank的NC_000081基因组区域的25,767位，对应于Tg编码序列的第19个外显子的第4,077位氨基酸(NM_009375 mRNA)。这个突变导致了第1,352位的异亮氨酸被赖氨酸替换，位置为p.I1352K。(来源：J:265197)
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
