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Motor Neurone Disease v0.181 FIG4 Bryony Thompson Marked gene: FIG4 as ready
Motor Neurone Disease v0.181 FIG4 Bryony Thompson Gene: fig4 has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.181 FIG4 Bryony Thompson Phenotypes for gene: FIG4 were changed from to Amyotrophic Lateral Sclerosis Type 11 (MONDO: 0012945; MIM#612577)
Motor Neurone Disease v0.180 FIG4 Bryony Thompson Mode of inheritance for gene: FIG4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Motor Neurone Disease v0.179 FIG4 Bryony Thompson Classified gene: FIG4 as Amber List (moderate evidence)
Motor Neurone Disease v0.179 FIG4 Bryony Thompson Added comment: Comment on list classification: Limited gene-disease validity assessment by ClinGen ALS spectrum disorders GCEP - 09/08/2022
Motor Neurone Disease v0.179 FIG4 Bryony Thompson Gene: fig4 has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.138 FIG4 Sangavi Sivagnanasundram reviewed gene: FIG4: Rating: GREEN; Mode of pathogenicity: None; Publications: 19118816, 20301623; Phenotypes: Amyotrophic Lateral Sclerosis Type 11 (MONDO: 0012945, MIM#612577); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Motor Neurone Disease v0.0 FIG4 Zornitza Stark gene: FIG4 was added
gene: FIG4 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: FIG4 was set to Unknown