Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4695
Gene Symbol: NDUFA2
NDUFA2
0.300 Biomarker disease CLINGEN Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathy. 28857146 2018
Entrez Id: 4695
Gene Symbol: NDUFA2
NDUFA2
0.300 Biomarker disease CLINGEN Accessory subunits are integral for assembly and function of human mitochondrial complex I. 27626371 2016
Entrez Id: 4695
Gene Symbol: NDUFA2
NDUFA2
0.300 Biomarker disease CLINGEN Whole exome sequencing in patients with white matter abnormalities. 27159321 2016
Entrez Id: 4695
Gene Symbol: NDUFA2
NDUFA2
0.300 Biomarker disease CLINGEN Protein carbonylation and adipocyte mitochondrial function. 22822087 2012
Entrez Id: 4695
Gene Symbol: NDUFA2
NDUFA2
0.300 Biomarker disease CLINGEN Region-specific expression of mitochondrial complex I genes during murine brain development. 21556144 2011
Entrez Id: 4695
Gene Symbol: NDUFA2
NDUFA2
0.300 Biomarker disease CLINGEN Subunits of mitochondrial complex I exist as part of matrix- and membrane-associated subcomplexes in living cells. 18826940 2008
Entrez Id: 4695
Gene Symbol: NDUFA2
NDUFA2
0.300 Biomarker disease CLINGEN NDUFA2 complex I mutation leads to Leigh disease. 18513682 2008
Entrez Id: 4695
Gene Symbol: NDUFA2
NDUFA2
0.300 Biomarker disease CLINGEN Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunits. 17209039 2007
Entrez Id: 4695
Gene Symbol: NDUFA2
NDUFA2
0.300 Biomarker disease CLINGEN cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed. 9878551 1998