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HOXB1
1 associated disease
6 protein interactions
UniProt info -
OMIM info -
Disease ODCs link
Congenital hereditary facial paralysis with variable hearing loss
Gene symbol Score
(click on to see the evidence)
PBX10.89
PAX60.75
NR3C10.72
CREBBP0.55
EP3000.55
SERPINA30.52