About   Help   FAQ
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
Loading...
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:  122 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory