CTR9

CTR9 homolog, Paf1/RNA polymerase II complex component
OMIM: 609366, Gene2Phenotype

3 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Green CTR9 in Childhood solid tumours Level 3: Childhood Tumours Level 2: Tumour syndromes Version 4.18 Latest signed off version: v4.0 (22 Mar 2023)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes Familial Wilms tumor Tags gene-checked
Green CTR9 in Intellectual disability - microarray and sequencing Level 3: Neurodevelopmental disorders Level 2: Neurology and neurodevelopmental disorders Version 5.531 Latest signed off version: v5.0 (22 Mar 2023) Component of the following Super Panels: Childhood onset leukodystrophy Hypotonic infant Paediatric disorders	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green NHS GMS Literature 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 Tags gene-checked
Green CTR9 in Wilms tumour with features suggestive of predisposition Version 1.3 Latest signed off version: v1.0 (30 Nov 2022)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Phenotypes Familial Wilms tumor Tags gene-checked