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Motor Neurone Disease v0.102 DYNC1H1 Zornitza Stark Marked gene: DYNC1H1 as ready
Motor Neurone Disease v0.102 DYNC1H1 Zornitza Stark Gene: dync1h1 has been classified as Red List (Low Evidence).
Motor Neurone Disease v0.102 DYNC1H1 Zornitza Stark Phenotypes for gene: DYNC1H1 were changed from to Spinal muscular atrophy, lower extremity-predominant 1, AD, MIM# 158600
Motor Neurone Disease v0.101 DYNC1H1 Zornitza Stark Mode of inheritance for gene: DYNC1H1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Motor Neurone Disease v0.100 DYNC1H1 Zornitza Stark Classified gene: DYNC1H1 as Red List (low evidence)
Motor Neurone Disease v0.100 DYNC1H1 Zornitza Stark Gene: dync1h1 has been classified as Red List (Low Evidence).
Motor Neurone Disease v0.99 DYNC1H1 Zornitza Stark reviewed gene: DYNC1H1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Spinal muscular atrophy, lower extremity-predominant 1, AD, MIM# 158600; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Motor Neurone Disease v0.0 DYNC1H1 Zornitza Stark gene: DYNC1H1 was added
gene: DYNC1H1 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: DYNC1H1 was set to Unknown