Symbol Name ID |
Polg
polymerase (DNA directed), gamma MGI:1196389 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Scapular winging |
Scoliosis |
Osteoporosis |
Disease(s) Associated with POLG | ||||
Alpers-Huttenlocher syndrome | ||||
autosomal recessive progressive external ophthalmoplegia 1 | ||||
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis |
Mouse Phenotypes | kyphosis |
osteoporosis |
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Availability | Mouse Genotype | ||
Polgtm1.1Lrsn/Polgtm1.1Lrsn | |||
Polgtm1Jiha/Polgtm1Jiha | |||
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 04/30/2024 MGI 6.23 |
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