Wilms tumour with features suggestive of predisposition
Gene: CTR9

CTR9 (CTR9 homolog, Paf1/RNA polymerase II complex component)
EnsemblGeneIds (GRCh38): ENSG00000198730
EnsemblGeneIds (GRCh37): ENSG00000198730
OMIM: 609366, Gene2Phenotype
CTR9 is in 4 panels

1 review

Eleanor Williams (Genomics England Curator)

This gene has been added to the panel on the recommendation of the NHS Genomic Medicine Service.
Created: 8 Mar 2022, 2:29 p.m. | Last Modified: 8 Mar 2022, 2:29 p.m.

Panel Version: 0.2

Created: 8 Mar 2022, 2:29 p.m.
Last Modified: 8 Mar 2022, 2:29 p.m.
Panel version: 0.2

Details

Mode of Inheritance

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Sources

Expert Review Green

Phenotypes

Familial Wilms tumor

Tags

gene-checked

OMIM

609366

Clinvar variants

Variants in CTR9

Penetrance

None

Publications

Panels with this gene

History Filter Activity

3 May 2022, Gel status: 3

Added Tag

Sarah Leigh (Genomics England Curator)

Tag gene-checked tag was added to gene: CTR9.

8 Mar 2022, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Eleanor Williams (Genomics England Curator)

gene: CTR9 was added gene: CTR9 was added to Wilms tumour with features suggestive of predisposition. Sources: Expert Review Green Mode of inheritance for gene: CTR9 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: CTR9 were set to 25099282; 29292210 Phenotypes for gene: CTR9 were set to Familial Wilms tumor

Wilms tumour with features suggestive of predisposition Gene: CTR9