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Date	Panel	Item	Activity
Filter activities 8 actions
10 May 2022	Intellectual disability - microarray and sequencing v3.1564	C8orf37	Arina Puzriakova commented on gene: C8orf37
10 May 2022	Intellectual disability - microarray and sequencing v3.1564	C8orf37	Arina Puzriakova Tag new-gene-name tag was added to gene: C8orf37.
30 Jan 2020	Intellectual disability - microarray and sequencing v3.0	C8orf37	Zornitza Stark changed review comment from: Two unrelated individuals reported with BBS; note gene has an association with retinal ciliopathies.; to: Two unrelated individuals reported with BBS; note gene has an association with retinal ciliopathies. Suggested rating Amber.
30 Jan 2020	Intellectual disability - microarray and sequencing v3.0	C8orf37	Zornitza Stark reviewed gene: C8orf37: Rating: ; Mode of pathogenicity: None; Publications: 26854863, 27008867; Phenotypes: Bardet-Biedl syndrome 21, MIM#617406; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
02 Aug 2017	Intellectual disability - microarray and sequencing	C8orf37	BRIDGE consortium edited their review of C8orf37
28 Jul 2017	Intellectual disability - microarray and sequencing	C8orf37	Louise Daugherty classified C8orf37 as amber
28 Jul 2017	Intellectual disability - microarray and sequencing	C8orf37	Louise Daugherty commented on C8orf37
27 Jul 2017	Intellectual disability - microarray and sequencing	C8orf37	BRIDGE consortium reviewed C8orf37