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Symbol
Name
ID
Polg
polymerase (DNA directed), gamma
MGI:1196389
Phenotype annotations related to skeleton
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
Availability Mouse Genotype
Polgtm1.1Lrsn/Polgtm1.1Lrsn
Polgtm1Jiha/Polgtm1Jiha
Polgtm1Prol/Polgtm1Prol

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
04/23/2024
MGI 6.23
The Jackson Laboratory