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Retinal disorders v8.97 DHX38 Eleanor Williams Tag Q3_25_promote_green was removed from gene: DHX38.
Retinal disorders v8.97 DHX38 Eleanor Williams reviewed gene: DHX38: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Retinal disorders v8.96 DHX38 Eleanor Williams Source Expert Review Green was added to DHX38.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v8.52 DHX38 Arina Puzriakova Classified gene: DHX38 as Amber List (moderate evidence)
Retinal disorders v8.52 DHX38 Arina Puzriakova Added comment: Comment on list classification: There is sufficient evidence to promote this gene to Green at the next GMS panel update - three different homozygous variants identified in four families with retinitis pigmentosa and a zebrafish knockout model supporting a role in retinal development (PMID: 24737827; 30208423; 35719279; 37867960)
Retinal disorders v8.52 DHX38 Arina Puzriakova Gene: dhx38 has been classified as Amber List (Moderate Evidence).
Retinal disorders v8.51 DHX38 Arina Puzriakova Publications for gene: DHX38 were set to 24737827; 30208423
Retinal disorders v8.50 DHX38 Arina Puzriakova Tag Q3_25_promote_green tag was added to gene: DHX38.
Retinal disorders v8.50 DHX38 Arina Puzriakova reviewed gene: DHX38: Rating: GREEN; Mode of pathogenicity: None; Publications: 24737827, 30208423, 35719279, 37867960; Phenotypes: Retinitis pigmentosa 84, OMIM:618220; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Retinal disorders v8.47 DHX38 Arina Puzriakova Phenotypes for gene: DHX38 were changed from Retinitis pigmentosa 84, 618220 to Retinitis pigmentosa 84, OMIM:618220
Retinal disorders v7.1 DHX38 Cassandra Smith reviewed gene: DHX38: Rating: AMBER; Mode of pathogenicity: None; Publications: 24737827, 30208423, 37867960; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
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