Genes in panel

Likely inborn error of metabolism - targeted testing not possible

Gene: NDUFS5

Red List (low evidence)

NDUFS5 (NADH:ubiquinone oxidoreductase subunit S5)
EnsemblGeneIds (GRCh38): ENSG00000168653
EnsemblGeneIds (GRCh37): ENSG00000168653
OMIM: 603847, Gene2Phenotype
NDUFS5 is in 4 panels

2 reviews

Ellen McDonagh (Genomics England Curator)

Comment on list classification: Candidate gene.
Created: 8 Feb 2016, 2:50 p.m.

Shamima Rahman (UCL Institute of Child Health)

I don't know

no pathogenic mutations reported to date but good candidate gene for mitochondrial complex I deficiency
Created: 3 Feb 2016, 5:31 p.m.


Mode of Inheritance
  • Expert Review Red
  • Mitochondrial Diseases
  • No OMIM phenotype
  • Isolated complex I deficiency
Clinvar variants
Variants in NDUFS5
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: NDUFS5 was added gene: NDUFS5 was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: NDUFS5 was set to Unknown Phenotypes for gene: NDUFS5 were set to Mitochondrial Diseases; No OMIM phenotype; Isolated complex I deficiency