Symbol Name ID |
Ghr
growth hormone receptor MGI:95708 |
Darker colors indicate more annotations |
Human Phenotypes | Xanthelasma |
Prolonged neonatal jaundice |
Sparse hair |
Hypohidrosis |
Prematurely aged appearance |
Premature skin wrinkling |
Tendon xanthomatosis |
Disease(s) Associated with GHR | |||||||
familial hypercholesterolemia | |||||||
isolated growth hormone deficiency | |||||||
Laron syndrome |
Mouse Phenotypes | increased subcutaneous adipose tissue amount |
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Availability | Mouse Genotype | |
Ghrtm1c(KOMP)Wtsi/Ghrtm1c(KOMP)Wtsi Tg(Fabp4-cre)1Rev/0 (conditional) |
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 04/30/2024 MGI 6.23 |
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