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Ciliopathies v0.123 CRELD1 Zornitza Stark Marked gene: CRELD1 as ready
Ciliopathies v0.123 CRELD1 Zornitza Stark Gene: creld1 has been classified as Red List (Low Evidence).
Ciliopathies v0.123 CRELD1 Zornitza Stark Phenotypes for gene: CRELD1 were changed from to Atrioventricular septal defect, partial, with heterotaxy syndrome 606217
Ciliopathies v0.122 CRELD1 Zornitza Stark Publications for gene: CRELD1 were set to
Ciliopathies v0.121 CRELD1 Zornitza Stark Mode of inheritance for gene: CRELD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Ciliopathies v0.120 CRELD1 Zornitza Stark Classified gene: CRELD1 as Red List (low evidence)
Ciliopathies v0.120 CRELD1 Zornitza Stark Gene: creld1 has been classified as Red List (Low Evidence).
Ciliopathies v0.103 CRELD1 Elena Savva reviewed gene: CRELD1: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 22740159; Phenotypes: {Atrioventricular septal defect, susceptibility to, 2} 606217, Atrioventricular septal defect, partial, with heterotaxy syndrome 606217; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Ciliopathies v0.0 CRELD1 Zornitza Stark gene: CRELD1 was added
gene: CRELD1 was added to Ciliopathies_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CRELD1 was set to Unknown