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Stroke v0.94 OTC Zornitza Stark Marked gene: OTC as ready
Stroke v0.94 OTC Zornitza Stark Gene: otc has been classified as Green List (High Evidence).
Stroke v0.94 OTC Zornitza Stark Phenotypes for gene: OTC were changed from Ornithine carbamoyltransferase deficiency to Ornithine carbamoyltransferase deficiency, MIM# 311250
Stroke v0.93 OTC Zornitza Stark Publications for gene: OTC were set to
Stroke v0.92 OTC Zornitza Stark Mode of inheritance for gene: OTC was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Stroke v0.91 OTC Zornitza Stark edited their review of gene: OTC: Changed rating: GREEN
Stroke v0.91 OTC Zornitza Stark reviewed gene: OTC: Rating: ; Mode of pathogenicity: None; Publications: 32008222, 24850570, 23640148; Phenotypes: Ornithine transcarbamylase deficiency, MIM# 311250; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Stroke v0.55 NOTCH3 Zornitza Stark Marked gene: NOTCH3 as ready
Stroke v0.55 NOTCH3 Zornitza Stark Gene: notch3 has been classified as Green List (High Evidence).
Stroke v0.55 NOTCH3 Zornitza Stark Publications for gene: NOTCH3 were set to
Stroke v0.54 NOTCH3 Zornitza Stark reviewed gene: NOTCH3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31960911; Phenotypes: Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1 125310; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Stroke v0.0 OTC Bryony Thompson gene: OTC was added
gene: OTC was added to Stroke. Sources: Expert Review Green,Royal Melbourne Hospital
Mode of inheritance for gene: OTC was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes for gene: OTC were set to Ornithine carbamoyltransferase deficiency
Stroke v0.0 NOTCH3 Bryony Thompson gene: NOTCH3 was added
gene: NOTCH3 was added to Stroke. Sources: Expert Review Green,Royal Melbourne Hospital
Mode of inheritance for gene: NOTCH3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: NOTCH3 were set to Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)