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Leprdb-rlpy
Spontaneous Allele Detail
Summary
Symbol: Leprdb-rlpy
Name: leptin receptor; rolypoly
MGI ID: MGI:2151180
Gene: Lepr  Location: Chr4:101574601-101672549 bp, + strand  Genetic Position: Chr4, 46.96 cM
Alliance: Leprdb-rlpy page
Mutation
origin
Strain of Origin:  NU/J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Deletion
  Leprdb-rlpy involves 1 genes/genome features (Lepr) View all
 
Mutation detailsThis allele is apparently a large genomic deletion involving the entire coding region of the gene. The closest flanking microsatellite markers, D4Mit176 (proximally) and D4Mit58 (distally) are present in homozygous mutant mice. (J:83762)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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:  121 strains or lines available
References
Original:  J:83762 Kim JH, et al., New leptin receptor mutations in mice: Lepr(db-rtnd), Lepr(db-dmpg) and Lepr(db-rlpy). J Nutr. 2003 May;133(5):1265-71
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