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Date	Panel	Item	Activity
Filter activities 6 actions
20 Jan 2022	Fetal anomalies v0.2563	SNX10	Zornitza Stark Marked gene: SNX10 as ready
20 Jan 2022	Fetal anomalies v0.2563	SNX10	Zornitza Stark Gene: snx10 has been classified as Red List (Low Evidence).
14 Jan 2022	Fetal anomalies v0.2197	SNX10	Chirag Patel Classified gene: SNX10 as Red List (low evidence)
14 Jan 2022	Fetal anomalies v0.2197	SNX10	Chirag Patel Gene: snx10 has been classified as Red List (Low Evidence).
14 Jan 2022	Fetal anomalies v0.2196	SNX10	Chirag Patel reviewed gene: SNX10: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
24 Oct 2021	Fetal anomalies v0.0	SNX10	Zornitza Stark gene: SNX10 was added gene: SNX10 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: SNX10 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SNX10 were set to Osteopetrosis, autosomal recessive 8, OMIM:615085; Autosomal recessive osteopetrosis 8, MONDO:0014040