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Intellectual disability - microarray and sequencing v3.1553 MSX1 Arina Puzriakova Phenotypes for gene: MSX1 were changed from Tooth agenesis, selective, 1, with or without orofacial cleft, 106600; Orofacial cleft 5, 608874; Ectodermal dysplasia 3, Witkop type, 189500 to Ectodermal dysplasia 3, Witkop type, OMIM:189500; Orofacial cleft 5, OMIM:608874; Tooth agenesis, selective, 1, with or without orofacial cleft, OMIM:106600
Intellectual disability - microarray and sequencing v3.421 MSX1 Arina Puzriakova Source Expert Review Red was added to MSX1.
Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
Intellectual disability - microarray and sequencing v3.253 MSX1 Arina Puzriakova commented on gene: MSX1
Intellectual disability - microarray and sequencing v3.3 MSX1 Zornitza Stark reviewed gene: MSX1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ectodermal dysplasia 3, Witkop type 189500, Orofacial cleft 5 608874, Tooth agenesis, selective, 1, with or without orofacial cleft 106600; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Intellectual disability - microarray and sequencing MSX1 BRIDGE consortium edited their review of MSX1
Intellectual disability - microarray and sequencing MSX1 Louise Daugherty classified MSX1 as amber
Intellectual disability - microarray and sequencing MSX1 Louise Daugherty commented on MSX1
Intellectual disability - microarray and sequencing MSX1 BRIDGE consortium reviewed MSX1