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Date	Panel	Item	Activity
Filter activities 4 actions
10 Mar 2026	Fetal anomalies v6.152	PLXNB2	Arina Puzriakova Added phenotypes amelogenesis imperfecta, hearing loss and intellectual disability for gene: PLXNB2
10 Mar 2026	Fetal anomalies v6.148	PLXNB2	Arina Puzriakova commented on gene: PLXNB2
10 Mar 2026	Fetal anomalies v6.147	PLXNB2	Vicki Harrison reviewed gene: PLXNB2: Rating: AMBER; Mode of pathogenicity: ; Publications: 38458752; Phenotypes: amelogenesis imperfecta, hearing loss and intellectual disability; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
09 Mar 2026	Fetal anomalies v6.146	PLXNB2	Arina Puzriakova gene: PLXNB2 was added gene: PLXNB2 was added to Fetal anomalies. Sources: Expert Review Amber Mode of inheritance for gene: PLXNB2 was set to BIALLELIC, autosomal or pseudoautosomal