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Date	Panel	Item	Activity
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12 Oct 2020	Intellectual disability - microarray and sequencing v3.421	KBTBD13	Arina Puzriakova Source Expert Review Red was added to KBTBD13. Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
17 Aug 2020	Intellectual disability - microarray and sequencing v3.252	KBTBD13	Arina Puzriakova commented on gene: KBTBD13
08 Feb 2020	Intellectual disability - microarray and sequencing v3.0	KBTBD13	Zornitza Stark reviewed gene: KBTBD13: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Nemaline myopathy 6, autosomal dominant, MIM# 609273; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
02 Aug 2017	Intellectual disability - microarray and sequencing	KBTBD13	BRIDGE consortium edited their review of KBTBD13
27 Jul 2017	Intellectual disability - microarray and sequencing	KBTBD13	BRIDGE consortium edited their review of KBTBD13
20 Jul 2017	Intellectual disability - microarray and sequencing	KBTBD13	Louise Daugherty classified KBTBD13 as amber
20 Jul 2017	Intellectual disability - microarray and sequencing	KBTBD13	Louise Daugherty commented on KBTBD13
19 Jul 2017	Intellectual disability - microarray and sequencing	KBTBD13	BRIDGE consortium reviewed KBTBD13