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Heterotaxy v1.8 STK36 Zornitza Stark Phenotypes for gene: STK36 were changed from Primary ciliary dyskinesia to Ciliary dyskinesia, primary, 46, MIM# 619436
Heterotaxy v1.7 STK36 Zornitza Stark edited their review of gene: STK36: Changed phenotypes: Ciliary dyskinesia, primary, 46, MIM# 619436
Heterotaxy v0.51 STK36 Zornitza Stark Marked gene: STK36 as ready
Heterotaxy v0.51 STK36 Zornitza Stark Gene: stk36 has been classified as Red List (Low Evidence).
Heterotaxy v0.51 STK36 Zornitza Stark Phenotypes for gene: STK36 were changed from to Primary ciliary dyskinesia
Heterotaxy v0.50 STK36 Zornitza Stark Publications for gene: STK36 were set to
Heterotaxy v0.49 STK36 Zornitza Stark Mode of inheritance for gene: STK36 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Heterotaxy v0.48 STK36 Zornitza Stark Classified gene: STK36 as Red List (low evidence)
Heterotaxy v0.48 STK36 Zornitza Stark Gene: stk36 has been classified as Red List (Low Evidence).
Heterotaxy v0.47 STK36 Zornitza Stark reviewed gene: STK36: Rating: RED; Mode of pathogenicity: None; Publications: 28543983; Phenotypes: Primary ciliary dyskinesia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Heterotaxy v0.0 STK36 Zornitza Stark gene: STK36 was added
gene: STK36 was added to Heterotaxy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: STK36 was set to Unknown