Optic neuropathy
Gene: OPA2Comment on list classification: demoted to Grey, this is a phenotype locus type symbolCreated: 16 Aug 2017, 10:43 a.m.
Added tag to explain why there is no Ensembl gene ID for this entity.Created: 6 Jan 2017, 4:34 p.m.
"Phenotype only" locus in HGNC (not classifed as a gene with protein product locus).Created: 7 Sep 2016, 10:57 a.m.
Mode of inheritance
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
Optic atrophy 2, X-linked
Tag curated_removed tag was added to gene: OPA2.
Tag ensembl_ids_known_missing tag was added to gene: OPA2.
This gene has been removed from the panel.
13.09.2016: 'Inherited optic neuropathies' was removed as a relevant disorder from the Posterior segment abnormalities gene panel (version 1.9) and this panel was approved to live. It has been internally reviewed and revised based on evidence available for each gene, and was promoted to version 1 to be used for analysis.
This gene has been classified as Red List (Low Evidence).
OPA2 was added to Inherited optic neuropathiespanel. Sources: Other
OPA2 was created by ellenmcdonagh