Retinal disordersGene: ARL2BP
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, 8:03 a.m.
Comment on mode of inheritance: sourced from OMIM.
Created: 15 Mar 2016, 10:46 a.m.
Source NHS GMS was added to ARL2BP. Rating Changed from Green List (high evidence) to Green List (high evidence)
This gene has been classified as Green List (High Evidence).
Mode of inheritance for ARL2BP was changed to BIALLELIC, autosomal or pseudoautosomal
ARL2BP was added to Posterior segment abnormalitiespanel. Sources: Expert Review Green
ARL2BP was created by ellenmcdonagh