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SNRPN
6 associated diseases
8 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Angelman syndrome
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
Prader-Willi syndrome due to translocation
Gene symbol Score
(click on to see the evidence)
TP530.73
ADAR0.63
EZH20.63
GIGYF20.63
HCFC10.63
PRPF30.63
SUZ120.63
GTF2I0.56