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Cholestasis v0.151 PEX7 Zornitza Stark Marked gene: PEX7 as ready
Cholestasis v0.151 PEX7 Zornitza Stark Gene: pex7 has been classified as Red List (Low Evidence).
Cholestasis v0.151 PEX7 Zornitza Stark Phenotypes for gene: PEX7 were changed from to Peroxisome biogenesis disorder 2A (Zellweger), MIM# 214110
Cholestasis v0.150 PEX7 Zornitza Stark Mode of inheritance for gene: PEX7 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Cholestasis v0.150 PEX7 Zornitza Stark Mode of inheritance for gene: PEX7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cholestasis v0.149 PEX7 Zornitza Stark Classified gene: PEX7 as Red List (low evidence)
Cholestasis v0.149 PEX7 Zornitza Stark Gene: pex7 has been classified as Red List (Low Evidence).
Cholestasis v0.148 PEX7 Zornitza Stark reviewed gene: PEX7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 2A (Zellweger), MIM# 214110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cholestasis v0.0 PEX7 Zornitza Stark gene: PEX7 was added
gene: PEX7 was added to Cholestasis_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: PEX7 was set to Unknown