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  2. BRIDGE_SPEED_NEURO_20170705
  3. CNOT3
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BRIDGE_SPEED_NEURO_20170705

Gene: CNOT3

Green List (high evidence)
CNOT3 (CCR4-NOT transcription complex subunit 3)
EnsemblGeneIds (GRCh38): ENSG00000088038
EnsemblGeneIds (GRCh37): ENSG00000088038
OMIM: 604910, Gene2Phenotype
CNOT3 is in 4 panels

2 reviews

BRIDGE consortium (NIHRBR-RD)

Green List (high evidence)

This is a pertinent gene from the NIHR BioResource - Rare Diseases Study (NIHRBR-RD) BRIDGE Study : SPEED (Specialist Pathology: Evaluating Exomes in Diagnostics) which covers epilepsies, movement and microcephaly disorders, this gene is on the SPEED_NEURO_20170705 gene list. Evidences used for SPEED NEURO gene list: in_ddg2p_2_4_2017;in_ddg2p_2_4_2017_conf . Main mutation mechanism : NA
Created: 28 Jul 2017, 8:56 a.m.

Mode of inheritance
Unknown

Publications

Created: 2 Aug 2017, 2:01 p.m.

Panel version: 0.191

Louise Daugherty (Genomics England Curator)

Comment on phenotypes: removed NA phenotype, to be reviewed if gene to be green on a panel that will be used in pipeline
Created: 31 Jul 2017, 9:42 a.m.
Created: 31 Jul 2017, 9:42 a.m.

Panel version: 0.39

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Green
  • BRIDGE study SPEED NEURO Tier1 Gene
OMIM
604910
Clinvar variants
Variants in CNOT3
Penetrance
Complete
Panels with this gene

History Filter Activity

31 Jul 2017, Gel status: 4

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Phenotypes for CNOT3 were set to

27 Jul 2017, Gel status: 4

Added New Source

Louise Daugherty (Genomics England Curator)

CNOT3 was added to BRIDGE_SPEED_NEURO_20170705panel. Sources: BRIDGE study SPEED NEURO Tier1 Gene,Expert Review Green

27 Jul 2017, Gel status: 0

Created

Louise Daugherty (Genomics England Curator)

CNOT3 was created by LouiseD