Activity

Filter

Cancel
Date Panel Item Activity
14 actions
Mendeliome v1.4691 NME8 Sangavi Sivagnanasundram Phenotypes for gene: NME8 were changed from Ciliary dyskinesia, primary, 6, MIM# 610852 to Ciliary dyskinesia, primary, 6, MIM# 610852; primary ciliary dyskinesia MONDO:0016575
Mendeliome v1.4690 NME8 Sangavi Sivagnanasundram Added comment: Comment on phenotypes: primary ciliary dyskinesia MONDO:0016575
Mendeliome v1.4690 NME8 Sangavi Sivagnanasundram Phenotypes for gene: NME8 were changed from Ciliary dyskinesia, primary, 6, MIM# 610852 to Ciliary dyskinesia, primary, 6, MIM# 610852
Mendeliome v1.4689 NME8 Sangavi Sivagnanasundram Tag disputed tag was added to gene: NME8.
Mendeliome v1.4689 NME8 Sangavi Sivagnanasundram reviewed gene: NME8: Rating: RED; Mode of pathogenicity: None; Publications: https://search.clinicalgenome.org/CCID:005652; Phenotypes: primary ciliary dyskinesia MONDO:0016575; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.2898 NME8 Zornitza Stark Marked gene: NME8 as ready
Mendeliome v0.2898 NME8 Zornitza Stark Gene: nme8 has been classified as Red List (Low Evidence).
Mendeliome v0.2898 NME8 Zornitza Stark Phenotypes for gene: NME8 were changed from to Ciliary dyskinesia, primary, 6, MIM# 610852
Mendeliome v0.2897 NME8 Zornitza Stark Publications for gene: NME8 were set to
Mendeliome v0.2896 NME8 Zornitza Stark Mode of inheritance for gene: NME8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.2895 NME8 Zornitza Stark Classified gene: NME8 as Red List (low evidence)
Mendeliome v0.2895 NME8 Zornitza Stark Gene: nme8 has been classified as Red List (Low Evidence).
Mendeliome v0.2890 NME8 Elena Savva reviewed gene: NME8: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 17360648; Phenotypes: Ciliary dyskinesia, primary, 6 610852; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.0 NME8 Zornitza Stark gene: NME8 was added
gene: NME8 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: NME8 was set to Unknown