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Motor Neurone Disease v2.0 TRIP4 Gene migrated from ENSG00000103671 to ENSG00000103671 (gene set migration)
Motor Neurone Disease v0.78 TRIP4 Zornitza Stark Marked gene: TRIP4 as ready
Motor Neurone Disease v0.78 TRIP4 Zornitza Stark Gene: trip4 has been classified as Red List (Low Evidence).
Motor Neurone Disease v0.78 TRIP4 Zornitza Stark Phenotypes for gene: TRIP4 were changed from to Spinal muscular atrophy with congenital bone fractures 1, MIM# 616866
Motor Neurone Disease v0.77 TRIP4 Zornitza Stark Publications for gene: TRIP4 were set to
Motor Neurone Disease v0.76 TRIP4 Zornitza Stark Mode of inheritance for gene: TRIP4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Motor Neurone Disease v0.75 TRIP4 Zornitza Stark Classified gene: TRIP4 as Red List (low evidence)
Motor Neurone Disease v0.75 TRIP4 Zornitza Stark Gene: trip4 has been classified as Red List (Low Evidence).
Motor Neurone Disease v0.74 TRIP4 Zornitza Stark reviewed gene: TRIP4: Rating: RED; Mode of pathogenicity: None; Publications: 26924529; Phenotypes: Spinal muscular atrophy with congenital bone fractures 1, MIM# 616866; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Motor Neurone Disease v0.28 TRIP4 Bryony Thompson Deleted their review
Motor Neurone Disease v0.0 TRIP4 Zornitza Stark gene: TRIP4 was added
gene: TRIP4 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: TRIP4 was set to Unknown