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  2. Possible mitochondrial disorder - nuclear genes
  3. COA1
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Possible mitochondrial disorder - nuclear genes

Gene: COA1

Amber List (moderate evidence)
COA1 (cytochrome c oxidase assembly factor 1 homolog)
EnsemblGeneIds (GRCh38): ENSG00000106603
EnsemblGeneIds (GRCh37): ENSG00000106603
OMIM: 614769, Gene2Phenotype
COA1 is in 4 panels

4 reviews

Carl Fratter (Oxford University Hospitals NHS Trust)

I don't know

Updated information and Amber review collated by Carl Fratter May 2019 on behalf of GMS mitochondrial specialist test group: no reports of human disease; complex IV assembly factor
Created: 10 May 2019, 1:02 p.m.

Mode of inheritance
Unknown

Phenotypes
No OMIM phenotype

Publications

  • none found

Created: 10 May 2019, 1:02 p.m.

Panel version: 0.134

Ivone Leong (Genomics England Curator)

Green List (high evidence)

Initial gene list and info collated by Carl Fratter (Oxford University Hospitals NHS Trust) January 2019 on behalf of the GMS Mitochondrial specialist test group.
Created: 4 Feb 2019, 1:36 p.m.

Mode of inheritance
Unknown

Phenotypes
No OMIM phenotype

Created: 4 Feb 2019, 1:36 p.m.

Panel version: 0.5

Ellen McDonagh (Genomics England Curator)

Comment when marking as ready: This gene should remain Amber due to the overall review and evidence assessment from the GMS mitochondrial specialist test group, submitted by Carl Fratter.
Created: 10 May 2019, 1:17 p.m.
Comment on list classification: This gene has been demoted to Amber until further evidence is provided. This gene is currently Red on the Mitochondrial disorders panel (code 112, Version 1.151) - further evidence needs to be submitted to support promoting this gene family member to Green.
Created: 29 Mar 2019, 2:23 p.m.
Comment when marking as ready: Candidate gene - should remain red.
Created: 26 Feb 2016, 3:45 p.m.
Created: 26 Feb 2016, 3:45 p.m.

Panel version: Imported from Mitochondrial disorders panel version 0.357

Shamima Rahman (UCL Institute of Child Health)

I don't know

aka C7orf44;

no mutation reports in literature but good candidate for complex IV deficiency (known assembly factor)
Created: 4 Feb 2016, 1:04 p.m.
Created: 4 Feb 2016, 1:04 p.m.

Panel version: Imported from Mitochondrial disorders panel version 0.16

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • No OMIM phenotype
OMIM
614769
Clinvar variants
Variants in COA1
Penetrance
None
Panels with this gene

History Filter Activity

10 May 2019, Gel status: 2

Entity classified by Genomics England curator

Ellen McDonagh (Genomics England Curator)

Gene: coa1 has been classified as Amber List (Moderate Evidence).

29 Mar 2019, Gel status: 2

Entity classified by Genomics England curator

Ellen McDonagh (Genomics England Curator)

Gene: coa1 has been classified as Amber List (Moderate Evidence).

4 Feb 2019, Gel status: 4

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

Ivone Leong (Genomics England Curator)

gene: COA1 was added gene: COA1 was added to Possible mitochondrial disorder - nuclear genes. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: COA1 was set to Unknown Phenotypes for gene: COA1 were set to No OMIM phenotype