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Wilms Tumour Predisposition v0.7 ASXL1 Zornitza Stark Marked gene: ASXL1 as ready
Wilms Tumour Predisposition v0.7 ASXL1 Zornitza Stark Gene: asxl1 has been classified as Green List (High Evidence).
Wilms Tumour Predisposition v0.7 ASXL1 Zornitza Stark Classified gene: ASXL1 as Green List (high evidence)
Wilms Tumour Predisposition v0.7 ASXL1 Zornitza Stark Gene: asxl1 has been classified as Green List (High Evidence).
Wilms Tumour Predisposition v0.6 ASXL1 Laura Raiti gene: ASXL1 was added
gene: ASXL1 was added to Wilms Tumour Predisposition. Sources: Literature
Mode of inheritance for gene: ASXL1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: ASXL1 were set to PMID: 29446906
Phenotypes for gene: ASXL1 were set to Bohring-Opitz syndrome , MIM#605039
Review for gene: ASXL1 was set to GREEN
Added comment: Isolated case reports suggest that individuals with BOS are at greater risk for Wilms tumor than the general population.
Recommended surveillance: Renal ultrasound every three months from birth to age eight to screen for the development of Wilms tumor; frequent monitoring of growth and development; close monitoring of feeding intolerance with a gastroenterology specialist; regular follow up for vision optimization.
Sources: Literature