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Amelogenesis imperfecta v2.0 CLDN16 Gene migrated from ENSG00000113946 to ENSG00000113946 (gene set migration)
Amelogenesis imperfecta v0.54 CLDN16 Zornitza Stark Phenotypes for gene: CLDN16 were changed from Hypomagnesemia 3, renal, MIM# 248250; Amelogenesis imperfecta to Hypomagnesaemia 3, renal, MIM# 248250; Amelogenesis imperfecta
Amelogenesis imperfecta v0.53 CLDN16 Zornitza Stark edited their review of gene: CLDN16: Changed phenotypes: Hypomagnesaemia 3, renal, MIM# 248250; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Amelogenesis imperfecta v0.53 CLDN16 Zornitza Stark Marked gene: CLDN16 as ready
Amelogenesis imperfecta v0.53 CLDN16 Zornitza Stark Gene: cldn16 has been classified as Green List (High Evidence).
Amelogenesis imperfecta v0.53 CLDN16 Zornitza Stark Phenotypes for gene: CLDN16 were changed from Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis (FHHNC) to Hypomagnesemia 3, renal, MIM# 248250; Amelogenesis imperfecta
Amelogenesis imperfecta v0.52 CLDN16 Zornitza Stark Classified gene: CLDN16 as Green List (high evidence)
Amelogenesis imperfecta v0.52 CLDN16 Zornitza Stark Gene: cldn16 has been classified as Green List (High Evidence).
Amelogenesis imperfecta v0.51 CLDN16 Zornitza Stark reviewed gene: CLDN16: Rating: GREEN; Mode of pathogenicity: None; Publications: 26426912; Phenotypes: Hypomagnesemia 3, renal, MIM# 248250; Mode of inheritance: None
Amelogenesis imperfecta v0.0 CLDN16 Zornitza Stark gene: CLDN16 was added
gene: CLDN16 was added to Amelogenesis imperfecta. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: CLDN16 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CLDN16 were set to 26426912
Phenotypes for gene: CLDN16 were set to Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis (FHHNC)