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BabyScreen+ newborn screening v1.114 CCDC39 Tommy Li Added phenotypes Ciliary dyskinesia, primary, 14, MIM# 613807 for gene: CCDC39
BabyScreen+ newborn screening v0.581 CCDC39 Zornitza Stark Marked gene: CCDC39 as ready
BabyScreen+ newborn screening v0.581 CCDC39 Zornitza Stark Gene: ccdc39 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.581 CCDC39 Zornitza Stark Phenotypes for gene: CCDC39 were changed from Primary ciliary dyskinesia to Ciliary dyskinesia, primary, 14, MIM# 613807
BabyScreen+ newborn screening v0.580 CCDC39 Zornitza Stark Classified gene: CCDC39 as Red List (low evidence)
BabyScreen+ newborn screening v0.580 CCDC39 Zornitza Stark Gene: ccdc39 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.579 CCDC39 Zornitza Stark reviewed gene: CCDC39: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ciliary dyskinesia, primary, 14, MIM# 613807; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 CCDC39 Zornitza Stark gene: CCDC39 was added
gene: CCDC39 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: CCDC39 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: CCDC39 were set to Primary ciliary dyskinesia