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| Wilms Tumour v0.40 | ASXL1 | Zornitza Stark Marked gene: ASXL1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wilms Tumour v0.40 | ASXL1 | Zornitza Stark Gene: asxl1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wilms Tumour v0.35 | ASXL1 |
Chirag Patel gene: ASXL1 was added gene: ASXL1 was added to Wilms Tumour. Sources: Expert list,Expert Review Mode of inheritance for gene: ASXL1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: ASXL1 were set to Wilms tumor, MONDO:0006058; Bohring-Opitz syndrome, MONDO:0011510; Bohring-Opitz syndrome, MIM#605039 Review for gene: ASXL1 was set to RED Added comment: Limited evidence for presentation with Wilms tumour in disease. Sources: Expert list, Expert Review |
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