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Polydactyly v0.36 ALX3 Anand Vasudevan reviewed gene: ALX3: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Polydactyly v0.29 ALX3 Zornitza Stark Classified gene: ALX3 as Red List (low evidence)
Polydactyly v0.29 ALX3 Zornitza Stark Gene: alx3 has been classified as Red List (Low Evidence).
Polydactyly v0.28 ALX3 Zornitza Stark edited their review of gene: ALX3: Added comment: Polydactyly not specifically associated with FND1. One family reported in 8362915, but polydactyly considered to be a separate feature.; Changed rating: RED; Changed publications: 19409524, 8362915
Polydactyly v0.28 ALX3 Zornitza Stark Marked gene: ALX3 as ready
Polydactyly v0.28 ALX3 Zornitza Stark Gene: alx3 has been classified as Green List (High Evidence).
Polydactyly v0.28 ALX3 Zornitza Stark Phenotypes for gene: ALX3 were changed from to Frontonasal dysplasia 1, MIM#136760
Polydactyly v0.27 ALX3 Zornitza Stark Publications for gene: ALX3 were set to
Polydactyly v0.26 ALX3 Zornitza Stark Mode of inheritance for gene: ALX3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Polydactyly v0.0 ALX3 Zornitza Stark gene: ALX3 was added
gene: ALX3 was added to Polydactyly_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ALX3 was set to Unknown