Glaucoma (developmental)
Gene: PLA2G5EnsemblGeneIds (GRCh38): ENSG00000127472
EnsemblGeneIds (GRCh37): ENSG00000127472
OMIM: 601192, Gene2Phenotype
PLA2G5 is in 3 panels
2 reviews
Nicola Ragge (Birmingham Women's and Children's NHS Foundation Hospital Trust)
retinal gene, can't find any evidence that it is associated with structural eye diseaseCreated: 19 Jun 2019, 3:32 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
[Fleck retina, familial benign]; 228980
Ivone Leong (Genomics England Curator)
Submitted on behalf of Professor Nicola Ragge (Wessex and West Midlands GLH). retinal gene, can't find any evidence that it is associated with structural eye diseaseCreated: 17 Apr 2019, 3:30 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
[Fleck retina, familial benign], 228980
Details
- Sources
-
- NHS GMS
- Emory Genetics Laboratory
- Phenotypes
-
- Eye Disorders
- OMIM
- 601192
- Clinvar variants
- Variants in PLA2G5
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
panel promoted to version 1
Ellen McDonagh (Genomics England Curator)27/04/2017: Revised after review and further curation, with clinical input, and promoted to version 1.
Added New Source
Eik Haraldsdottir (Genomics England)PLA2G5 was added to Glaucoma (developmental)panel. Sources: Emory Genetics Laboratory