Genomics England
GMS Panels
Panels
Genes and Entities

CTR9

CTR9 homolog, Paf1/RNA polymerase II complex component
OMIM: 609366
PanelMode of inheritanceDetails
4 panels
Green
in Childhood solid tumours
R-numbers: R359
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Familial Wilms tumor
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CTR9-related neurodevelopmental disorder
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 8.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Macrocephaly, HP:0000256, Motor delay, HP:0001270, intellectual disability, MONDO:0001071, Delayed speech and language development, Behavioral abnormality, Autistic behavior, Failure to thrive, Feeding difficulties, Abnormality of the cardiovascular system
Green
in Wilms tumour with features suggestive of predisposition
R-numbers: R220
Signed-off version 1.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Familial Wilms tumor