Cytoscape Web
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LRP5
8 associated diseases
5 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Autosomal dominant osteopetrosis type 1
Autosomal dominant osteosclerosis, Worth type
Familial exudative vitreoretinopathy
Hyperostosis corticalis generalisata
Idiopathic juvenile osteoporosis
Osteoporosis - pseudoglioma
Osteosclerosis - developmental delay - craniosynostosis
Retinopathy of prematurity
Gene symbol Score
(click on to see the evidence)
SOST0.68
DKK10.65
NDP0.63
SMAD90.63
WNT10.52