Gene: POLG ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.600 GeneticVariation disease UNIPROT POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement. 15477547 2004
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.600 GeneticVariation disease UNIPROT Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia. 12565911 2003
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.600 GeneticVariation disease UNIPROT Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO). 12707443 2003
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.600 GeneticVariation disease UNIPROT Digenic progressive external ophthalmoplegia in a sporadic patient: recessive mutations in POLG and C10orf2/Twinkle. 12872260 2003
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.600 GeneticVariation disease UNIPROT POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions. 14635118 2003
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.600 GeneticVariation disease UNIPROT Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma. 12975295 2003
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.600 CausalMutation disease CLINVAR Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions. 11431686 2001
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.600 GeneticVariation disease UNIPROT Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions. 11431686 2001
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.600 GeneticVariation disease CLINVAR