DISEASES

Disease-gene associations mined from literature

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Literature associating GRXCR2 and autosomal dominant nonsyndromic deafness 54

GRXCR2 [ENSP00000367214]

Glutaredoxin domain-containing cysteine-rich protein 2; Could play a role in maintaining cochlear stereocilia bundles that are involved in sound detection.

Synonyms:  GRXCR2,  GRXCR2p,  hGRXCR2,  A0A1W2PQQ7,  A6NFK2 ...

Linkouts:  STRING  Pharos  UniProt  OMIM

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.