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This spontaneous mutation involves the deletion of a single nucleotide in exon 11 (GRCm39:chr4:101628503delT) in the cytokine receptor homology 2 (CRH2) leptin-binding domain of the encoded peptide, which causes a frameshift and premature stop codon (p.L536Hfs*6). (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
