Mitochondrial disorders
Gene: ATP5HThe rating of this gene has been updated from Amber to Red following NHS Genomic Medicine Service approval.Created: 29 Jul 2022, 1:47 p.m. | Last Modified: 29 Jul 2022, 1:47 p.m.
Panel Version: 2.109
Cannot find evidence for Mendelian gene-disease association in humans.Created: 18 Mar 2020, 6:39 a.m. | Last Modified: 18 Mar 2020, 6:39 a.m.
Panel Version: 2.5
Added new-gene-name tag, new approved HGNC gene symbol for ATP5H is ATP5PDCreated: 18 Dec 2019, 3:36 p.m. | Last Modified: 18 Dec 2019, 3:36 p.m.
Panel Version: 2.3
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: 23 Jul 2019, 10:13 a.m. | Last Modified: 23 Jul 2019, 10:13 a.m.
Panel Version: 1.412
Source Expert Review Red was added to ATP5H. Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
Tag new-gene-name tag was added to gene: ATP5H.
gene: ATP5H was added gene: ATP5H was added to Mitochondrial disorders. Sources: NHS GMS,Expert Review Amber Mode of inheritance for gene: ATP5H was set to Unknown Phenotypes for gene: ATP5H were set to No OMIM phenotype