Cytoscape Web
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GJB2
8 associated diseases
3 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Hypotrichosis-deafness syndrome
Keratoderma hereditarium mutilans
KID syndrome
Knuckle pads-leuconychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome
Palmoplantar keratoderma-deafness syndrome
Porokeratotic eccrine ostial and dermal duct nevus
Gene symbol Score
(click on to see the evidence)
CAV10.84
GJB10.62
GJB60.59