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Cerebellar and Pontocerebellar Hypoplasia v0.99 OPHN1 Zornitza Stark Marked gene: OPHN1 as ready
Cerebellar and Pontocerebellar Hypoplasia v0.99 OPHN1 Zornitza Stark Gene: ophn1 has been classified as Green List (High Evidence).
Cerebellar and Pontocerebellar Hypoplasia v0.99 OPHN1 Zornitza Stark Phenotypes for gene: OPHN1 were changed from to Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance, MIM# 300486
Cerebellar and Pontocerebellar Hypoplasia v0.98 OPHN1 Zornitza Stark Publications for gene: OPHN1 were set to
Cerebellar and Pontocerebellar Hypoplasia v0.97 OPHN1 Zornitza Stark Mode of inheritance for gene: OPHN1 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cerebellar and Pontocerebellar Hypoplasia v0.96 OPHN1 Zornitza Stark reviewed gene: OPHN1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20528889, 9582072, 12807966, 16221952; Phenotypes: Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance, MIM# 300486; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cerebellar and Pontocerebellar Hypoplasia v0.0 OPHN1 Zornitza Stark gene: OPHN1 was added
gene: OPHN1 was added to Cerebellar and Pontocerebellar hypoplasia_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: OPHN1 was set to Unknown