Activity

Filter

Cancel
Date Panel Item Activity
8 actions
Monogenic hearing loss v2.31 ELMOD3 Eleanor Williams Phenotypes for gene: ELMOD3 were changed from ?Deafness, autosomal recessive 88, 615429 to ?Deafness, autosomal recessive 88, 615429; Deafness, autosomal dominant
Monogenic hearing loss v2.30 ELMOD3 Eleanor Williams Publications for gene: ELMOD3 were set to
Monogenic hearing loss v2.29 ELMOD3 Eleanor Williams Mode of inheritance for gene: ELMOD3 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Monogenic hearing loss v2.28 ELMOD3 Eleanor Williams Classified gene: ELMOD3 as Amber List (moderate evidence)
Monogenic hearing loss v2.28 ELMOD3 Eleanor Williams Added comment: Comment on list classification: Although there are 2 SNV cases plus a mouse model the mode of inheritance differs. In another case there is a multigene deletion. Promoting from red to amber for now, and will wait for further cases to determine clarity on the mode of inheritance. Amber rating supported by the Genomics England clinical team.
Monogenic hearing loss v2.28 ELMOD3 Eleanor Williams Gene: elmod3 has been classified as Amber List (Moderate Evidence).
Monogenic hearing loss v2.4 ELMOD3 Eleanor Williams reviewed gene: ELMOD3: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Monogenic hearing loss v2.4 ELMOD3 Zornitza Stark reviewed gene: ELMOD3: Rating: AMBER; Mode of pathogenicity: None; Publications: 240396609, 31628468, 30284680, 29713870; Phenotypes: Deafness, autosomal recessive 88, MIM#615429, Deafness, autosomal dominant; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal