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Retinal disorders v1.159 DHX38 Gavin Arno reviewed gene: DHX38: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Retinal disorders v1.137 DHX38 Ivone Leong Source NHS GMS was added to DHX38.
Retinal disorders v1.109 DHX38 Ivone Leong Classified gene: DHX38 as Amber List (moderate evidence)
Retinal disorders v1.109 DHX38 Ivone Leong Added comment: Comment on list classification: Promoted from red to amber. DHX38 is associated with a phenotype in OMIM but not Gene2Phenotype. PMID: 24737827 reports 4 affected siblings from a consanguineous Pakistani family with early-onset retinitis pigmentosa and macular coloboma who have homozygous c.995G>A variant (G332). No functional studies were performed. PMID: 30208423 reports 2 different consanguineous Pakistani family who have members affected by early-onset retinitis pigmentosa. The authors found that the affected members had homozygous c.971G>A variants (R324Q). No functional studies were performed. Based on this evidence, it was decided that the gene should be promoted to an amber rating.
Retinal disorders v1.109 DHX38 Ivone Leong Gene: dhx38 has been classified as Amber List (Moderate Evidence).
Retinal disorders v1.107 DHX38 Ivone Leong Publications for gene: DHX38 were set to
Retinal disorders v1.106 DHX38 Ivone Leong Mode of inheritance for gene: DHX38 was changed from to BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v1.105 DHX38 Ivone Leong Phenotypes for gene: DHX38 were changed from No OMIM disease ID to Retinitis pigmentosa 84, 618220