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Retinal disorders

Gene: CEP19

Amber List (moderate evidence)

CEP19 (centrosomal protein 19)
EnsemblGeneIds (GRCh38): ENSG00000174007
EnsemblGeneIds (GRCh37): ENSG00000174007
OMIM: 615586, Gene2Phenotype
CEP19 is in 2 panels

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 CEP19
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: CEP19 was added gene: CEP19 was added to Retinal disorders. Sources: Expert Review Amber,RetNet,NHS GMS Mode of inheritance for gene: CEP19 was set to