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PNPT1
2 associated diseases
3 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Combined oxidative phosphorylation defect type 13
Gene symbol Score
(click on to see the evidence)
TRAF60.63
HSPB10.49
PRKCSH0.49