DISEASES

Disease-gene associations mined from literature

Literature associating WFS1 and autosomal recessive nonsyndromic deafness 4

WFS1 [ENSP00000226760]

Wolfram syndrome 1 (wolframin); Participates in the regulation of cellular Ca(2+) homeostasis, at least partly, by modulating the filling state of the endoplasmic reticulum Ca(2+) store; Deafness associated genes

Synonyms:  WFS1,  WFS1p,  hWFS1,  B4DJ99,  O76024 ...

Linkouts:  STRING  Pharos  UniProt  OMIM