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Mendeliome v2.0 CRPPA Gene symbol changed from ISPD to CRPPA during gene set migration (ENSG00000214960 -> ENSG00000214960)
Mendeliome v1.3806 ISPD Lucy Spencer Phenotypes for gene: ISPD were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, MIM# 614643; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7, MIM# 616052 to Myopathy caused by variation in CRPPA MONDO:0100530; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, MIM# 614643; Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7, MIM# 616052
Mendeliome v1.3805 ISPD Lucy Spencer reviewed gene: ISPD: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Myopathy caused by variation in CRPPA MONDO:0100530; Mode of inheritance: None
Mendeliome v1.2944 ISPD Zornitza Stark Added comment: Comment when marking as ready: New HGNC approved name is CRPPA.