Gene: COX1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4512
Gene Symbol: COX1
COX1 		0.600 GermlineCausalMutation disease ORPHANET MELAS-like encephalomyopathy caused by a new pathogenic mutation in the mitochondrial DNA encoded cytochrome c oxidase subunit I. 22832341 2012
Entrez Id: 4512
Gene Symbol: COX1
COX1 		0.600 GermlineCausalMutation disease ORPHANET A novel mitochondrial DNA mutation in COX1 leads to strokes, seizures, and lactic acidosis. 19568996 2008
Entrez Id: 4512
Gene Symbol: COX1
COX1 		0.600 CausalMutation disease CLINVAR A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness. 8019558 1994
Entrez Id: 4512
Gene Symbol: COX1
COX1 		0.600 Biomarker disease CTD_human