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Severe Paediatric Disorders v0.17 HSPB8 Louise Daugherty Mode of inheritance for gene HSPB8 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Severe Paediatric Disorders v0.12 HSPB8 Louise Daugherty reviewed gene: HSPB8: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 HSPB8 Louise Daugherty Publications for gene HSPB8 were updated from to 30847515
Severe Paediatric Disorders v0.10 HSPB8 Louise Daugherty Added phenotypes Charcot-Marie-Tooth disease, axonal, type 2L, 608673; Neuropathy, distal hereditary motor, type IIA, 158590 for gene: HSPB8
Severe Paediatric Disorders v0.9 HSPB8 Louise Daugherty Added phenotypes Charcot-Marie-Tooth disease, axonal, type 2L, 608673; Neuropathy, distal hereditary motor, type IIA, 158590 for gene: HSPB8
Severe Paediatric Disorders v0.9 HSPB8 Louise Daugherty Added phenotypes Charcot-Marie-Tooth disease, axonal, type 2L, 608673; Neuropathy, distal hereditary motor, type IIA, 158590 for gene: HSPB8
Severe Paediatric Disorders v0.8 HSPB8 Louise Daugherty Added phenotypes Neuropathy, distal hereditary motor, type IIA, 158590; Charcot-Marie-Tooth disease, axonal, type 2L, 608673 for gene: HSPB8
Severe Paediatric Disorders v0.7 HSPB8 Louise Daugherty Source Next Generation Children Project was added to HSPB8.
Severe Paediatric Disorders v0.5 HSPB8 Louise Daugherty Source Expert Review Green was added to HSPB8.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 HSPB8 Louise Daugherty gene: HSPB8 was added
gene: HSPB8 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: HSPB8 was set to