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Monogenic hearing loss v4.62 SOX2 Achchuthan Shanmugasundram Tag for-review was removed from gene: SOX2.
Tag to_be_confirmed_NHSE was removed from gene: SOX2.
Monogenic hearing loss v4.62 SOX2 Achchuthan Shanmugasundram reviewed gene: SOX2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Monogenic hearing loss v4.61 SOX2 Achchuthan Shanmugasundram Source NHS GMS was added to SOX2.
Source Expert Review Amber was added to SOX2.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Monogenic hearing loss v2.218 SOX2 Eleanor Williams Tag to_be_confirmed_NHSE tag was added to gene: SOX2.
Monogenic hearing loss v2.65 SOX2 Eleanor Williams Tag for-review tag was added to gene: SOX2.
Monogenic hearing loss v2.65 SOX2 Eleanor Williams Classified gene: SOX2 as Green List (high evidence)
Monogenic hearing loss v2.65 SOX2 Eleanor Williams Added comment: Comment on list classification: Limited evidence for green rating. Should be reviewed at the next major review of this panel.
Monogenic hearing loss v2.65 SOX2 Eleanor Williams Gene: sox2 has been classified as Green List (High Evidence).
Monogenic hearing loss v2.64 SOX2 Eleanor Williams Publications for gene: SOX2 were set to PMID:10564870; 11135495; 12002146; 12036291; 12461687; 12612584; 14517545; 15240551; 15346919; 15389708; 15812812; 15846349; 16145681; 16283891; 16470798; 16543359; 16651659; 16712695; 16892407; 16904174; 16932809; 17015430; 17219395; 17515932; 17522155; 17554336; 17554338; 18029452; 18157115; 18285410; 18385377; 18806776; 18818365; 18831064; 18845712; 19254784; 19403656; 19801978; 19898493; 19921648; 20803647; 21326281; 21331042; 21532573; 21919124; 24048479; 24909994; 7849401; 8741917
Monogenic hearing loss v2.63 SOX2 Eleanor Williams edited their review of gene: SOX2: Changed rating: AMBER
Monogenic hearing loss v2.63 SOX2 Eleanor Williams commented on gene: SOX2
Monogenic hearing loss v2.4 SOX2 Zornitza Stark reviewed gene: SOX2: Rating: AMBER; Mode of pathogenicity: None; Publications: 30262714, 16932809, 16145681; Phenotypes: Microphthalmia, syndromic 3, MIM# 206900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted