Symbol Name ID |
Lepr
leptin receptor MGI:104993 |
* | 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 | * |
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 |
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