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| Wilms Tumour v0.40 | CTCF | Zornitza Stark Marked gene: CTCF as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wilms Tumour v0.40 | CTCF | Zornitza Stark Gene: ctcf has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wilms Tumour v0.36 | CTCF |
Chirag Patel 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 Added comment: 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, Literature |
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