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Motor Neurone Disease v0.159 ASCC1 Zornitza Stark Marked gene: ASCC1 as ready
Motor Neurone Disease v0.159 ASCC1 Zornitza Stark Gene: ascc1 has been classified as Green List (High Evidence).
Motor Neurone Disease v0.159 ASCC1 Zornitza Stark Phenotypes for gene: ASCC1 were changed from to spinal muscular atrophy with congenital bone fractures 2 (MONDO:0014807; MIM#616867)
Motor Neurone Disease v0.158 ASCC1 Zornitza Stark Publications for gene: ASCC1 were set to
Motor Neurone Disease v0.157 ASCC1 Zornitza Stark Mode of inheritance for gene: ASCC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Motor Neurone Disease v0.138 ASCC1 Sangavi Sivagnanasundram reviewed gene: ASCC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26924529, 28218388; Phenotypes: spinal muscular atrophy with congenital bone fractures 2 (MONDO:0014807, MIM#616867); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Motor Neurone Disease v0.13 ASCC1 Bryony Thompson Deleted their review
Motor Neurone Disease v0.0 ASCC1 Zornitza Stark gene: ASCC1 was added
gene: ASCC1 was added to Motor neuron disease MND_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Complex Neurology Flagship
Mode of inheritance for gene: ASCC1 was set to Unknown