BRIDGE_SPEED_NEURO_v2.0_20160416
Gene: CCT5

CCT5 (chaperonin containing TCP1 subunit 5)
EnsemblGeneIds (GRCh38): ENSG00000150753
EnsemblGeneIds (GRCh37): ENSG00000150753
OMIM: 610150, Gene2Phenotype
CCT5 is in 11 panels

1 review

BRIDGE consortium (NIHRBR-RD)

Green List (high evidence)

omim_20150205_movement; manju_list; neuro_20160418_strict; NA
Created: 7 Feb 2017, 4:14 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Neuropathy, hereditary sensory, with spastic paraplegia, 256840

Variants in this GENE are reported as part of current diagnostic practice

Created: 7 Feb 2017, 4:14 p.m.

Panel version: 0.2

Details

Mode of Inheritance

BIALLELIC, autosomal or pseudoautosomal

Sources

BRIDGE

Phenotypes

Neuropathy, hereditary sensory, with spastic paraplegia, 256840

OMIM

610150

Clinvar variants

Variants in CCT5

Penetrance

Complete

Panels with this gene

History Filter Activity

7 Feb 2017, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

CCT5 was added to BRIDGE_SPEED_NEURO_v2.0_20160416panel. Sources: BRIDGE

7 Feb 2017, Gel status: 0

Created