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Retinal disorders v6.7 JAG1 Sarah Leigh Tag Q1_24_promote_green was removed from gene: JAG1.
Tag Q1_24_NHS_review was removed from gene: JAG1.
Retinal disorders v6.7 JAG1 Eleanor Williams reviewed gene: JAG1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinal disorders v6.6 JAG1 Sarah Leigh Source Expert Review Green was added to JAG1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Retinal disorders v4.77 JAG1 Achchuthan Shanmugasundram Classified gene: JAG1 as Amber List (moderate evidence)
Retinal disorders v4.77 JAG1 Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available for the promotion of this gene to green rating in the next GMS review.
Retinal disorders v4.77 JAG1 Achchuthan Shanmugasundram Gene: jag1 has been classified as Amber List (Moderate Evidence).
Retinal disorders v4.76 JAG1 Achchuthan Shanmugasundram Phenotypes for gene: JAG1 were changed from Alagille syndrome 1, OMIM:118450 to Alagille syndrome 1, OMIM:118450; exudative vitreoretinopathy, MONDO:0019516
Retinal disorders v4.75 JAG1 Achchuthan Shanmugasundram Publications for gene: JAG1 were set to
Retinal disorders v4.74 JAG1 Achchuthan Shanmugasundram Tag Q1_24_promote_green tag was added to gene: JAG1.
Tag Q1_24_NHS_review tag was added to gene: JAG1.
Retinal disorders v4.74 JAG1 Achchuthan Shanmugasundram reviewed gene: JAG1: Rating: GREEN; Mode of pathogenicity: None; Publications: 31273345, 34185059; Phenotypes: Alagille syndrome 1, OMIM:118450, exudative vitreoretinopathy, MONDO:0019516; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinal disorders v4.71 JAG1 Siying Lin changed review comment from: Well-demarcated peripheral chorioretinal atrophic changes appear to be a not infrequent finding in patiets with Alagille syndrome, and have also been seen in within our inherited retinal dystrophy clinical cohort.; to: Well-demarcated peripheral chorioretinal atrophic changes appear to be a not infrequent finding in patiets with Alagille syndrome, and these retinal findings have also been seen in at least 2 unrelated patients with Alagille syndrome within our inherited retinal dystrophy clinical cohort
Retinal disorders v4.71 JAG1 Siying Lin reviewed gene: JAG1: Rating: GREEN; Mode of pathogenicity: Other; Publications: PMID: 34185059; Phenotypes: Retinal dystrophy, peripheral chorioretial atrophy, Alagille syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinal disorders v2.208 JAG1 Arina Puzriakova Phenotypes for gene: JAG1 were changed from to Alagille syndrome 1, OMIM:118450
Retinal disorders v2.207 JAG1 Arina Puzriakova Mode of inheritance for gene: JAG1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinal disorders v2.5 JAG1 Ivone Leong reviewed gene: JAG1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Retinal disorders v2.3 JAG1 Ivone Leong gene: JAG1 was added
gene: JAG1 was added to Retinal disorders. Sources: Expert Review Amber,RetNet,NHS GMS
Mode of inheritance for gene: JAG1 was set to