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Malformations of cortical development v3.11 B4GAT1 Arina Puzriakova Tag Q3_21_rating was removed from gene: B4GAT1.
Malformations of cortical development v3.11 B4GAT1 Arina Puzriakova reviewed gene: B4GAT1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Malformations of cortical development v3.10 B4GAT1 Arina Puzriakova Source Expert Review Green was added to B4GAT1.
Source NHS GMS was added to B4GAT1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Malformations of cortical development v2.59 B4GAT1 Ivone Leong Tag Q3_21_rating tag was added to gene: B4GAT1.
Malformations of cortical development v2.59 B4GAT1 Ivone Leong Classified gene: B4GAT1 as Amber List (moderate evidence)
Malformations of cortical development v2.59 B4GAT1 Ivone Leong Added comment: Comment on list classification: This gene is associated with a relevant phenotype in OMIM but not in Gene2Phenotype. There is enough evidence to support a gene-disease association. This gene should be rated Green at the next review.
Malformations of cortical development v2.59 B4GAT1 Ivone Leong Gene: b4gat1 has been classified as Amber List (Moderate Evidence).
Malformations of cortical development v2.58 B4GAT1 Ivone Leong Publications for gene: B4GAT1 were set to 23359570; 23877401; 23359570; 23217742
Malformations of cortical development v2.57 B4GAT1 Ivone Leong Phenotypes for gene: B4GAT1 were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 615287 to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13, OMIM:615287
Malformations of cortical development v2.56 B4GAT1 Ivone Leong Publications for gene: B4GAT1 were set to 23359570
Malformations of cortical development v2.7 B4GAT1 Zornitza Stark reviewed gene: B4GAT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23359570, 23877401, 23359570, 23217742; Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13 MIM# 615287; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Malformations of cortical development B4GAT1 Alice Gardham marked B4GAT1 as ready
Malformations of cortical development B4GAT1 Alice Gardham added B4GAT1 to panel
Malformations of cortical development B4GAT1 Alice Gardham reviewed B4GAT1