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Monogenic hearing loss v2.243 CISD2 Arina Puzriakova Mode of inheritance for gene: CISD2 was changed from to BIALLELIC, autosomal or pseudoautosomal
Monogenic hearing loss v2.225 CISD2 Eleanor Williams Phenotypes for gene: CISD2 were changed from hearing loss; Wolfram syndrome 2 604928 to hearing loss; Wolfram syndrome 2, OMIM:604928
Monogenic hearing loss v2.224 CISD2 Eleanor Williams Tag for-review was removed from gene: CISD2.
Monogenic hearing loss v2.221 CISD2 Eleanor Williams commented on gene: CISD2: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Monogenic hearing loss v2.220 CISD2 Eleanor Williams Source Expert Review Green was added to CISD2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Monogenic hearing loss v2.52 CISD2 Eleanor Williams Tag for-review tag was added to gene: CISD2.
Monogenic hearing loss v2.52 CISD2 Eleanor Williams Classified gene: CISD2 as Amber List (moderate evidence)
Monogenic hearing loss v2.52 CISD2 Eleanor Williams Added comment: Comment on list classification: Promoting this gene from red to amber as several cases reported with hearing loss as a feature, but not as the first presenting feature.
Monogenic hearing loss v2.52 CISD2 Eleanor Williams Gene: cisd2 has been classified as Amber List (Moderate Evidence).
Monogenic hearing loss v2.51 CISD2 Eleanor Williams Phenotypes for gene: CISD2 were changed from hearing loss to hearing loss; Wolfram syndrome 2 604928
Monogenic hearing loss v2.50 CISD2 Eleanor Williams Publications for gene: CISD2 were set to
Monogenic hearing loss v2.49 CISD2 Eleanor Williams edited their review of gene: CISD2: Changed rating: AMBER; Changed publications: 10739754, 17846994, 25056293, 25371195; Changed phenotypes: Wolfram syndrome 2 #604928; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Monogenic hearing loss v2.49 CISD2 Eleanor Williams commented on gene: CISD2
Monogenic hearing loss v2.4 CISD2 Zornitza Stark reviewed gene: CISD2: Rating: GREEN; Mode of pathogenicity: None; Publications: 25371195; Phenotypes: Wolfram syndrome 2, MIM# 604928; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes