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BabyScreen+ newborn screening v0.365 MOCS2 Zornitza Stark Marked gene: MOCS2 as ready
BabyScreen+ newborn screening v0.365 MOCS2 Zornitza Stark Gene: mocs2 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.365 MOCS2 Zornitza Stark Phenotypes for gene: MOCS2 were changed from Molybdenum cofactor deficiency to Molybdenum cofactor deficiency B, MIM#252160
BabyScreen+ newborn screening v0.364 MOCS2 Zornitza Stark Classified gene: MOCS2 as Red List (low evidence)
BabyScreen+ newborn screening v0.364 MOCS2 Zornitza Stark Gene: mocs2 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.363 MOCS2 Zornitza Stark reviewed gene: MOCS2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Molybdenum cofactor deficiency B MIM#252160; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.274 MOCS2 David Amor reviewed gene: MOCS2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: molybdenum cofactor deficiency B; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 MOCS2 Zornitza Stark gene: MOCS2 was added
gene: MOCS2 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: MOCS2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MOCS2 were set to Molybdenum cofactor deficiency