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Hand and foot malformations v0.70 HOXD13 Zornitza Stark Marked gene: HOXD13 as ready
Hand and foot malformations v0.70 HOXD13 Zornitza Stark Gene: hoxd13 has been classified as Green List (High Evidence).
Hand and foot malformations v0.70 HOXD13 Zornitza Stark Phenotypes for gene: HOXD13 were changed from brachydactyly to Brachydactyly, type E 113300 Brachydactyly, type D, MIM# 113200; Syndactyly, type V, MIM# 186300; Synpolydactyly 1, MIM# 186000; Brachydactyly-syndactyly syndrome, MIM# 610713
Hand and foot malformations v0.69 HOXD13 Zornitza Stark Publications for gene: HOXD13 were set to 12649808; 17236141
Hand and foot malformations v0.68 HOXD13 Zornitza Stark Mode of inheritance for gene: HOXD13 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Hand and foot malformations v0.67 HOXD13 Zornitza Stark Mode of inheritance for gene: HOXD13 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hand and foot malformations v0.66 HOXD13 Zornitza Stark Classified gene: HOXD13 as Green List (high evidence)
Hand and foot malformations v0.66 HOXD13 Zornitza Stark Gene: hoxd13 has been classified as Green List (High Evidence).
Hand and foot malformations v0.65 HOXD13 Zornitza Stark reviewed gene: HOXD13: Rating: GREEN; Mode of pathogenicity: None; Publications: 34777468, 32509852; Phenotypes: Brachydactyly, type E 113300 Brachydactyly, type D, MIM# 113200, Syndactyly, type V, MIM# 186300, Synpolydactyly 1, MIM# 186000, Brachydactyly-syndactyly syndrome, MIM# 610713; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Hand and foot malformations v0.62 HOXD13 Sue White gene: HOXD13 was added
gene: HOXD13 was added to Hand and foot malformations. Sources: Literature
Mode of inheritance for gene: HOXD13 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: HOXD13 were set to 12649808; 17236141
Phenotypes for gene: HOXD13 were set to brachydactyly