Cytoscape Web
Click node...

MAGEL2
4 associated diseases
2 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Prader-Willi syndrome due to imprinting mutation
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
Gene symbol Score
(click on to see the evidence)
TRIM270.78
VPS350.63