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Severe Paediatric Disorders v0.12 XYLT2 Louise Daugherty reviewed gene: XYLT2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 XYLT2 Louise Daugherty Publications for gene XYLT2 were updated from to 30847515
Severe Paediatric Disorders v0.10 XYLT2 Louise Daugherty Added phenotypes Spondyloocular syndrome, 605822 for gene: XYLT2
Severe Paediatric Disorders v0.9 XYLT2 Louise Daugherty Added phenotypes Spondyloocular syndrome, 605822 for gene: XYLT2
Severe Paediatric Disorders v0.9 XYLT2 Louise Daugherty Added phenotypes Spondyloocular syndrome, 605822 for gene: XYLT2
Severe Paediatric Disorders v0.8 XYLT2 Louise Daugherty Added phenotypes Spondyloocular syndrome, 605822 for gene: XYLT2
Severe Paediatric Disorders v0.8 XYLT2 Louise Daugherty Mode of inheritance for gene XYLT2 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Spondyloocular syndrome, 605822 for gene: XYLT2
Severe Paediatric Disorders v0.7 XYLT2 Louise Daugherty Source Next Generation Children Project was added to XYLT2.
Severe Paediatric Disorders v0.5 XYLT2 Louise Daugherty Source Expert Review Green was added to XYLT2.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 XYLT2 Louise Daugherty gene: XYLT2 was added
gene: XYLT2 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: XYLT2 was set to