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Lepm1Yst
Chemically induced Allele Detail
Summary
Symbol: Lepm1Yst
Name: leptin; mutation 1, Yau-Sheng Tsai
MGI ID: MGI:4880027
Synonyms: Leptin145E
Gene: Lep  Location: Chr6:29060220-29073875 bp, + strand  Genetic Position: Chr6, 12.3 cM
Alliance: Lepm1Yst page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutatgenesis induced a T to A transversion in exon 3 that results in the amino acid substitution of glutamic acid for valine at position 145 (V145E). (J:167736)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 7 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Lep Mutation:  19 strains or lines available
References
Original:  J:167736 Hong CJ, et al., ENU mutagenesis identifies mice with morbid obesity and severe hyperinsulinemia caused by a novel mutation in leptin. PLoS One. 2010;5(12):e15333
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
04/16/2024
MGI 6.23
The Jackson Laboratory