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LeprKK
Spontaneous Allele Detail
Summary
Symbol: LeprKK
Name: leptin receptor; KK
MGI ID: MGI:2182842
Synonyms: ASP600Asn
Gene: Lepr  Location: Chr4:101574601-101672549 bp, + strand  Genetic Position: Chr4, 46.96 cM
Alliance: LeprKK page
Mutation
origin
Strain of Origin:  KK
Mutation
description
Allele Type:    Spontaneous
Mutation:    Nucleotide substitutions
 
Mutation detailsSequence analysis of the Lepr gene in the hyperinsulinemic KK mouse strain identified a conservative amino acid substitution; Asp(600)Asn in a highly conserved area of the protein. Data suggests that the variant contributes to the obesity phenotype seen in mice, but that the contribution is only part of a multigenic syndrome. (J:53637)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Lepr Mutation:  122 strains or lines available
References
Original:  J:53637 Igel M, et al., Hyperleptinemia and leptin receptor variant Asp600Asn in the obese, hyperinsulinemic KK mouse strain. J Mol Endocrinol. 1998 Dec;21(3):337-45
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory