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Motor Neurone Disease v0.96 ATP7A Zornitza Stark Marked gene: ATP7A as ready
Motor Neurone Disease v0.96 ATP7A Zornitza Stark Gene: atp7a has been classified as Red List (Low Evidence).
Motor Neurone Disease v0.96 ATP7A Zornitza Stark Phenotypes for gene: ATP7A were changed from to Spinal muscular atrophy, distal, X-linked 3, 300489
Motor Neurone Disease v0.95 ATP7A Zornitza Stark Mode of inheritance for gene: ATP7A was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Motor Neurone Disease v0.94 ATP7A Zornitza Stark Classified gene: ATP7A as Red List (low evidence)
Motor Neurone Disease v0.94 ATP7A Zornitza Stark Gene: atp7a has been classified as Red List (Low Evidence).
Motor Neurone Disease v0.93 ATP7A Zornitza Stark reviewed gene: ATP7A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Spinal muscular atrophy, distal, X-linked 3, 300489; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Motor Neurone Disease v0.0 ATP7A Zornitza Stark gene: ATP7A was added
gene: ATP7A 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: ATP7A was set to Unknown