Symbol Name ID |
Gh
growth hormone MGI:95707 |
Darker colors indicate more annotations |
Human Phenotypes | Elevated red cell adenosine deaminase activity |
Abnormality of iron homeostasis |
Decreased level of 1,5 anhydroglucitol in serum |
Hyperglycemia |
Hypoglycemia |
Neonatal hypoglycemia |
Diabetes mellitus |
Type I diabetes mellitus |
Insulin resistance |
Ketoacidosis |
Nonimmune hydrops fetalis |
Abnormality of temperature regulation |
Decreased circulating parathyroid hormone level |
Aortic valve calcification |
Mitral valve calcification |
Decreased serum leptin |
Reduced circulating growth hormone concentration |
Decreased serum insulin-like growth factor 1 |
Ectopic calcification |
Disease(s) Associated with GH1 | |||||||||||||||||||
autoimmune polyendocrine syndrome type 1 | |||||||||||||||||||
beta thalassemia | |||||||||||||||||||
Diamond-Blackfan anemia | |||||||||||||||||||
isolated growth hormone deficiency | |||||||||||||||||||
isolated growth hormone deficiency type IA | |||||||||||||||||||
isolated growth hormone deficiency type IB | |||||||||||||||||||
isolated growth hormone deficiency type II | |||||||||||||||||||
progeria | |||||||||||||||||||
type 1 diabetes mellitus |
Mouse Phenotypes | decreased fasting circulating glucose level |
increased circulating ghrelin level |
impaired glucose tolerance |
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Availability | Mouse Genotype | |||
GhSma1/GhSma1 | ||||
Ghtm1.1(KOMP)Vlcg/Ghtm1.1(KOMP)Vlcg |
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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