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Symbol
Name
ID
Ghr
growth hormone receptor
MGI:95708
Phenotype annotations related to integument
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
Availability Mouse Genotype
Ghrtm1c(KOMP)Wtsi/Ghrtm1c(KOMP)Wtsi
Tg(Fabp4-cre)1Rev/0  (conditional)

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
04/30/2024
MGI 6.23
The Jackson Laboratory