Genes in panel

Likely inborn error of metabolism - targeted testing not possible

Gene: NDUFA7

Red List (low evidence)

NDUFA7 (NADH:ubiquinone oxidoreductase subunit A7)
EnsemblGeneIds (GRCh38): ENSG00000267855
EnsemblGeneIds (GRCh37): ENSG00000267855
OMIM: 602139, Gene2Phenotype
NDUFA7 is in 4 panels

1 review

Shamima Rahman (UCL Institute of Child Health)

I don't know

no mutation reports in literature; good candidate gene for complex I deficiency (encodes a subunit of the enzyme)

Created: 4 Feb 2016, 7:03 p.m.


Mode of Inheritance
  • Expert Review Red
  • No OMIM phenotype
  • Isolated complex I deficiency
Clinvar variants
Variants in NDUFA7
Panels with this gene

History Filter Activity

8 Jan 2019, Gel status: 1

Panel promoted to version 1.0

Ellen McDonagh (Genomics England Curator)

Sarah Leigh: Associated with phenotype in O

16 Dec 2018, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: NDUFA7 was added gene: NDUFA7 was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: NDUFA7 was set to Unknown Phenotypes for gene: NDUFA7 were set to No OMIM phenotype; Isolated complex I deficiency