Wilms Tumour
Gene: CTCFEnsemblGeneIds (GRCh38): ENSG00000102974
EnsemblGeneIds (GRCh37): ENSG00000102974
OMIM: 604167, Gene2Phenotype
CTCF is in 7 panels
1 review
Chirag Patel (Genetic Health Queensland)
Limited evidence for presentation with Wilms tumour in disease. Four cases of Wilms tumour in unrelated individuals with CTCF-related disorder.
Sources: Expert list, Expert Review, LiteratureCreated: 26 Sep 2024, 1:45 a.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Wilms tumor, MONDO:0006058; Intellectual developmental disorder, autosomal dominant 21, MIM#615502
Publications
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Red
- Literature
- Expert Review
- Expert list
- Phenotypes
-
- Wilms tumor, MONDO:0006058
- Intellectual developmental disorder, autosomal dominant 21, MIM#615502
- OMIM
- 604167
- Clinvar variants
- Variants in CTCF
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: ctcf has been classified as Red List (Low Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Chirag Patel (Genetic Health Queensland)gene: CTCF was added gene: CTCF was added to Wilms Tumour. Sources: Expert list,Expert Review,Literature Mode of inheritance for gene: CTCF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: CTCF were set to PMID: 31239556, 35459888, 36454652 Phenotypes for gene: CTCF were set to Wilms tumor, MONDO:0006058; Intellectual developmental disorder, autosomal dominant 21, MIM#615502 Review for gene: CTCF was set to RED