Gene: NDUFS6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4726
Gene Symbol: NDUFS6
NDUFS6 		0.710 Biomarker disease GENOMICS_ENGLAND New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre. 27290639 2016
Entrez Id: 4726
Gene Symbol: NDUFS6
NDUFS6 		0.710 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 4726
Gene Symbol: NDUFS6
NDUFS6 		0.710 Biomarker disease MGD Tissue-specific splicing of an Ndufs6 gene-trap insertion generates a mitochondrial complex I deficiency-specific cardiomyopathy. 22474353 2012
Entrez Id: 4726
Gene Symbol: NDUFS6
NDUFS6 		0.710 GeneticVariation disease BEFREE Tissue-specific splicing of an Ndufs6 gene-trap insertion generates a mitochondrial complex I deficiency-specific cardiomyopathy. 22474353 2012
Entrez Id: 4726
Gene Symbol: NDUFS6
NDUFS6 		0.710 GermlineCausalMutation disease ORPHANET Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases. 22644603 2012
Entrez Id: 4726
Gene Symbol: NDUFS6
NDUFS6 		0.710 GermlineCausalMutation disease ORPHANET Mutated NDUFS6 is the cause of fatal neonatal lactic acidemia in Caucasus Jews. 19259137 2009
Entrez Id: 4726
Gene Symbol: NDUFS6
NDUFS6 		0.710 GermlineCausalMutation disease ORPHANET NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency. 15372108 2004
Entrez Id: 4726
Gene Symbol: NDUFS6
NDUFS6 		0.710 Biomarker disease GENOMICS_ENGLAND