CNOT3

CCR4-NOT transcription complex subunit 3
OMIM: 604910, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green CNOT3 in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.205	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, MIM# 618672
Green CNOT3 in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, MIM# 618672
Green CNOT3 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genetic Health Queensland Phenotypes Intellectual developmental disorder with speech delay, autism, and dysmorphic facies 618672
Amber CNOT3 in Cerebral vascular malformations Level 2: Neurology and neurodevelopmental disorders Version 1.0 Component of the following Super Panels: Progressive Neurological Conditions	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Moya Moya Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, MIM# 618672
Green CNOT3 in Fetal anomalies Version 1.313	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Intellectual developmental disorder with speech delay, autism, and dysmorphic facies , MIM#618672