Genes in panel
STRs in panel
Prev Next

Mitochondrial disorders

Gene: COX6C

Red List (low evidence)

COX6C (cytochrome c oxidase subunit 6C)
EnsemblGeneIds (GRCh38): ENSG00000164919
EnsemblGeneIds (GRCh37): ENSG00000164919
OMIM: 124090, Gene2Phenotype
COX6C 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 IV deficiency (encodes a subunit of the enzyme)
Created: 4 Feb 2016, 1:24 p.m.

Details

Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • No OMIM phenotype
OMIM
124090
Clinvar variants
Variants in COX6C
Penetrance
Complete
Panels with this gene

History Filter Activity

30 Jun 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

COX6C was added to All recognised syndromes and those with suggestive featurespanel. Sources: Radboud University Medical Center, Nijmegen