Retinal disorders
Gene: MERTKEnsemblGeneIds (GRCh38): ENSG00000153208
EnsemblGeneIds (GRCh37): ENSG00000153208
OMIM: 604705, Gene2Phenotype
MERTK is in 3 panels
3 reviews
Gavin Arno (UCL Institute of Ophthalmology/Moorfields Eye Hospital)
BRIDGE consortium (NIHRBR-RD)
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Retinitis pigmentosa 38
Variants in this GENE are reported as part of current diagnostic practice
Ellen McDonagh (Genomics England Curator)
This gene is on the Manchester Genetic Retinal Degeneration Conditions panel (covers known genes for isolated progessive retinal degeneration, Leber congenital amaurosis, macular dystrophy, achromatopsia, congenital stationary night blindness as well as the two most common causes of syndromic blindess Usher and Bardet-Biedl syndromes and additional syndromes including Joubert, Senior-Loken, and Cohen syndrome.Created: 2 Jun 2016, 8:04 a.m.
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- NHS GMS
- Expert Review Green
- Phenotypes
-
- Retinitis pigmentosa 38
- childhood onset rod-cone dystrophy with early macular atrophy
- Leber congenital amaurosis
- Retinitis pigmentosa 38
- Eye Disorders
- Retinitis pigmentosa
- Retinitis Pigmentosa, Recessive
- Retinitis pigmentosa 38, 613862
- OMIM
- 604705
- Clinvar variants
- Variants in MERTK
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
Added New Source, Status Update
Ivone Leong (Genomics England Curator)Source NHS GMS was added to MERTK. Rating Changed from Green List (high evidence) to Green List (high evidence)
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Created
Ellen McDonagh (Genomics England Curator)MERTK was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)MERTK was added to Posterior segment abnormalitiespanel. Sources: Expert Review Green