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ERLIN2
3 associated diseases
10 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Autosomal recessive spastic paraplegia type 18
Juvenile primary lateral sclerosis
Recessive intellectual disability - motor dysfunction - multiple joint contractures
Gene symbol Score
(click on to see the evidence)
ITPR10.73
FN10.72
CD3D0.63
CFTR0.63
CLN30.63
PSEN10.63
RNF1390.63
TCF30.63
UFD1L0.63
EEF20.49