Symbol Name ID |
Gh
growth hormone MGI:95707 |
Darker colors indicate more annotations |
Human Phenotypes | Hepatomegaly |
Hepatitis |
Chronic active hepatitis |
Cholelithiasis |
Prolonged neonatal jaundice |
Disease(s) Associated with GH1 | |||||
autoimmune polyendocrine syndrome type 1 | |||||
beta thalassemia | |||||
isolated growth hormone deficiency | |||||
isolated growth hormone deficiency type IA |
Mouse Phenotypes | decreased liver weight |
small liver |
|
Availability | Mouse Genotype | ||
GhSma1/GhSma1 | |||
Ghtm1.1(KOMP)Vlcg/Ghtm1.1(KOMP)Vlcg | |||
GhSma1/Gh+ |
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 05/28/2024 MGI 6.13 |
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