Mitochondrial disorder with complex III deficiency
Gene: UQCR10Comment on list classification: Demoting to Red as there is no evidence for Mendelian gene-disease association at this timeCreated: 29 Jul 2022, 1:02 p.m. | Last Modified: 29 Jul 2022, 1:02 p.m.
Panel Version: 1.6
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, 10:56 a.m.
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 III subunitCreated: 10 May 2019, 10:51 a.m.
Mode of inheritance
Unknown
Phenotypes
No OMIM phenotype
Publications
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. Gene Symbol submitted: UQCR10; Suggested intial gene rating: Green.Created: 1 Feb 2019, 4:33 p.m.
Mode of inheritance
Unknown
Phenotypes
No OMIM phenotype
Gene: uqcr10 has been classified as Red List (Low Evidence).
Gene: uqcr10 has been classified as Amber List (Moderate Evidence).
Gene: uqcr10 has been classified as Amber List (Moderate Evidence).
gene: UQCR10 was added gene: UQCR10 was added to Mitochondrial disorder with complex III deficiency. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: UQCR10 was set to Unknown Phenotypes for gene: UQCR10 were set to No OMIM phenotype