Gene: COX20 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 116228
Gene Symbol: COX20
COX20 		0.710 GeneticVariation disease UNIPROT The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis. 29154948 2018
Entrez Id: 116228
Gene Symbol: COX20
COX20 		0.710 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 116228
Gene Symbol: COX20
COX20 		0.710 GeneticVariation disease UNIPROT Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation. 24202787 2014
Entrez Id: 116228
Gene Symbol: COX20
COX20 		0.710 Biomarker disease BEFREE These results establish the function of the human gene FAM36A/COX20 in complex IV assembly and support a causal role of the gene in complex IV deficiency. 23125284 2013
Entrez Id: 116228
Gene Symbol: COX20
COX20 		0.710 GeneticVariation disease UNIPROT These results establish the function of the human gene FAM36A/COX20 in complex IV assembly and support a causal role of the gene in complex IV deficiency. 23125284 2013
Entrez Id: 116228
Gene Symbol: COX20
COX20 		0.710 GermlineCausalMutation disease ORPHANET These results establish the function of the human gene FAM36A/COX20 in complex IV assembly and support a causal role of the gene in complex IV deficiency. 23125284 2013
Entrez Id: 116228
Gene Symbol: COX20
COX20 		0.710 Biomarker disease CTD_human
Entrez Id: 116228
Gene Symbol: COX20
COX20 		0.710 CausalMutation disease CLINVAR
Entrez Id: 116228
Gene Symbol: COX20
COX20 		0.710 Biomarker disease GENOMICS_ENGLAND