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Regression v0.257 INPP5E Zornitza Stark Marked gene: INPP5E as ready
Regression v0.257 INPP5E Zornitza Stark Gene: inpp5e has been classified as Red List (Low Evidence).
Regression v0.257 INPP5E Zornitza Stark Phenotypes for gene: INPP5E were changed from to Joubert syndrome 1, MIM# 213300; MONDO:0008944; Mental retardation, truncal obesity, retinal dystrophy, and micropenis, MIM# 610156; MONDO:0012423
Regression v0.256 INPP5E Zornitza Stark Publications for gene: INPP5E were set to
Regression v0.255 INPP5E Zornitza Stark Mode of inheritance for gene: INPP5E was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Regression v0.254 INPP5E Zornitza Stark Classified gene: INPP5E as Red List (low evidence)
Regression v0.254 INPP5E Zornitza Stark Gene: inpp5e has been classified as Red List (Low Evidence).
Regression v0.253 INPP5E Zornitza Stark reviewed gene: INPP5E: Rating: RED; Mode of pathogenicity: None; Publications: 19668216, 32139166, 29230161, 29052317, 27998989, 27401686, 19668215; Phenotypes: Joubert syndrome 1, MIM# 213300, MONDO:0008944, Mental retardation, truncal obesity, retinal dystrophy, and micropenis, MIM# 610156, MONDO:0012423; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Regression v0.0 INPP5E Zornitza Stark gene: INPP5E was added
gene: INPP5E was added to Regression_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: INPP5E was set to Unknown