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Retinal disorders

Gene: CCT2

Amber List (moderate evidence)

CCT2 (chaperonin containing TCP1 subunit 2)
EnsemblGeneIds (GRCh38): ENSG00000166226
EnsemblGeneIds (GRCh37): ENSG00000166226
OMIM: 605139, Gene2Phenotype
CCT2 is in 1 panel

1 review

Ivone Leong (Genomics England Curator)

I don't know

Submitted on behalf of the GMS Eye specialist group. These genes are also from RetNet. There is currently not enough evidence to rate these genes Green, therefore they have been given an Amber rating.
Created: 27 Dec 2019, 9:10 a.m. | Last Modified: 27 Dec 2019, 9:10 a.m.
Panel Version: 2.5


  • RetNet
  • Expert Review Amber
Clinvar variants
Variants in CCT2
Panels with this gene

History Filter Activity

27 Dec 2019, Gel status: 2

Created, Added New Source, Set mode of inheritance

Ivone Leong (Genomics England Curator)

gene: CCT2 was added gene: CCT2 was added to Retinal disorders. Sources: Expert Review Amber,RetNet,NHS GMS Mode of inheritance for gene: CCT2 was set to