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| Wilms Tumour v0.40 | CDC73 | Zornitza Stark Marked gene: CDC73 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wilms Tumour v0.40 | CDC73 | Zornitza Stark Gene: cdc73 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wilms Tumour v0.37 | CDC73 |
Chirag Patel gene: CDC73 was added gene: CDC73 was added to Wilms Tumour. Sources: Expert list,Expert Review,Literature Mode of inheritance for gene: CDC73 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: CDC73 were set to PMID: 37339334, 7912571, 7717405 Phenotypes for gene: CDC73 were set to Wilms tumor, MONDO:0006058; Hyperparathyroidism 2 with jaw tumors, MONDO:0007768; Hyperparathyroidism-jaw tumor syndrome, MIM#145001; Hyperparathyroidism, familial primary, MIM#145000 Review for gene: CDC73 was set to RED Added comment: ClinGen definitive. Limited evidence for presentation with Wilms tumour in disease. Three cases of Wilms tumour in unrelated individuals with HPT-JT syndrome. Sources: Expert list, Expert Review, Literature |
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