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中文
这种自发突变涉及到编码肽中细胞因子受体同源区(CRH2)的 leptin 结合域，具体在exon 11的单个碱基缺失（GRCm39:chr4:101628503delT），导致了移位和早停密码子（p.L536Hfs*6）。(来源：J:313303)
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
