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Symbol Name ID |
Polg
polymerase (DNA directed), gamma MGI:1196389 |
| Darker colors indicate more annotations |
| Human Phenotypes | Intestinal pseudo-obstruction |
Constipation |
Diarrhea |
Nausea |
Vomiting |
Dysphagia |
Gastrointestinal dysmotility |
Hepatocellular carcinoma |
| Disease(s) Associated with POLG | ||||||||
| Alpers-Huttenlocher syndrome | ||||||||
| autosomal dominant progressive external ophthalmoplegia 1 | ||||||||
| autosomal recessive progressive external ophthalmoplegia 1 | ||||||||
| hepatocellular carcinoma | ||||||||
| mitochondrial DNA depletion syndrome 4b | ||||||||
| Parkinson's disease | ||||||||
| sensory ataxic neuropathy, dysarthria, and ophthalmoparesis |
| Mouse Phenotypes | abnormal crypts of Lieberkuhn morphology |
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| Availability | Mouse Genotype | |
| Polgtm1Prol/Polgtm1Prol | ||
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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