POLG
protein-coding gene in the species Homo sapiens
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Summary
POLG is a gene[1].
Key Facts
- Subclass of: protein-coding gene[2]
- HomoloGene ID: 2016[3]
- Genomic start: 89305198[4], 89859534[5]
- Genomic end: 89334861[6], 89878092[7]
- Ortholog: Polg[8], MIP1[9], tam[10], polg-1[11]
- Encodes: DNA polymerase gamma, catalytic subunit[12], DNA polymerase subunit gamma-1[13]
- Found in taxon: Homo sapiens[14]
- Chromosome: human chromosome 15[15]
- Genetic association: progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1[16], mitochondrial DNA depletion syndrome 4b[17], autosomal dominant progressive external ophthalmoplegia[18], sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome[19], autosomal recessive progressive external ophthalmoplegia[20], mitochondrial neurogastrointestinal encephalomyopathy[21], Alpers' disease[22]
- Strand orientation: reverse strand[23]
- Cytogenetic location: 15q26.1[24]
- Expressed in: granulocyte[25], tibial nerve[26], transverse colon[27], body of stomach[28], right lobe of thyroid gland[29], body of pancreas[30], spleen[31], apex of heart[32], body of uterus[33], minor salivary glands[34]