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Hereditary Spastic Paraplegia - paediatric v0.209 SLC1A4 Zornitza Stark Phenotypes for gene: SLC1A4 were changed from Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, 616657 to Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, 616657; MONDO:0014725
Hereditary Spastic Paraplegia - paediatric v0.208 SLC1A4 Zornitza Stark Tag founder tag was added to gene: SLC1A4.
Hereditary Spastic Paraplegia - paediatric v0.208 SLC1A4 Zornitza Stark Marked gene: SLC1A4 as ready
Hereditary Spastic Paraplegia - paediatric v0.208 SLC1A4 Zornitza Stark Gene: slc1a4 has been classified as Green List (High Evidence).
Hereditary Spastic Paraplegia - paediatric v0.208 SLC1A4 Zornitza Stark Publications for gene: SLC1A4 were set to
Hereditary Spastic Paraplegia - paediatric v0.207 SLC1A4 Zornitza Stark reviewed gene: SLC1A4: Rating: GREEN; Mode of pathogenicity: None; Publications: 25930971, 26138499, 26041762, 27193218, 29989513; Phenotypes: Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, MIM# 616657; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary Spastic Paraplegia - paediatric v0.0 SLC1A4 Bryony Thompson gene: SLC1A4 was added
gene: SLC1A4 was added to Hereditary Spastic Paraplegia - paediatric_RMH. Sources: Expert Review Green,Royal Melbourne Hospital
Mode of inheritance for gene: SLC1A4 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: SLC1A4 were set to Spastic tetraplegia, thin corpus callosum, and progressive microcephaly, 616657