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Symbol
Name
ID
Lepr
leptin receptor
MGI:104993
Phenotype annotations related to skeleton
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Osteoporosis
Gout
Disease(s) Associated with LEPR
coronary artery disease
osteoporosis

Mouse Phenotypes
skeleton phenotype
abnormal osteoclast differentiation
short femur
short tibia
abnormal pelvic girdle bone morphology
abnormal bone structure
decreased bone mineral content
decreased bone mineral density
increased bone volume
abnormal skeleton development
Availability Mouse Genotype
Leprdb/Leprdb
Leprm8Btlr/Leprm8Btlr
Leprtm1b(EUCOMM)Wtsi/Leprtm1b(EUCOMM)Wtsi
Leprtm4Mgmj/Leprtm4Mgmj
Tg(Apoe-Lepr)1Kry/0 *

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