Cytoscape Web
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OCA2
5 associated diseases
1 protein interaction
UniProt info -
OMIM info -
Disease ODCs link
Angelman syndrome
Oculocutaneous albinism type 2
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)
ATP13A20.72