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Monogenic hearing loss v2.233 SLC12A2 Eleanor Williams Tag for-review was removed from gene: SLC12A2.
Monogenic hearing loss v2.221 SLC12A2 Eleanor Williams commented on gene: SLC12A2
Monogenic hearing loss v2.220 SLC12A2 Eleanor Williams Source Expert Review Green was added to SLC12A2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Monogenic hearing loss v2.49 SLC12A2 Arina Puzriakova Phenotypes for gene: SLC12A2 were changed from to Bilateral sensorineural hearing loss; Intellectual disability; Secretory defects
Monogenic hearing loss v2.48 SLC12A2 Arina Puzriakova Publications for gene: SLC12A2 were set to
Monogenic hearing loss v2.47 SLC12A2 Arina Puzriakova Mode of inheritance for gene: SLC12A2 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Monogenic hearing loss v2.46 SLC12A2 Arina Puzriakova Classified gene: SLC12A2 as Amber List (moderate evidence)
Monogenic hearing loss v2.46 SLC12A2 Arina Puzriakova Added comment: Comment on list classification: There is sufficient evidence to rate this gene GREEN at the next major review - at least 10 unrelated cases (and animal models) presenting significant sensorineural hearing loss, associated with variants in SLC12A2.
Monogenic hearing loss v2.46 SLC12A2 Arina Puzriakova Gene: slc12a2 has been classified as Amber List (Moderate Evidence).
Monogenic hearing loss v2.45 SLC12A2 Arina Puzriakova Tag for-review tag was added to gene: SLC12A2.
Monogenic hearing loss v2.45 SLC12A2 Arina Puzriakova reviewed gene: SLC12A2: Rating: GREEN; Mode of pathogenicity: None; Publications: 30740830, 32294086, 32754646, 32658972; Phenotypes: Bilateral sensorineural hearing loss, Intellectual disability, Secretory defects; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Monogenic hearing loss v2.18 SLC12A2 Zornitza Stark reviewed gene: SLC12A2: Rating: GREEN; Mode of pathogenicity: None; Publications: 32294086; Phenotypes: Congenital, severe to profound hearing loss; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes