DISEASES

Disease-gene associations mined from literature

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Literature associating SLC44A2 and autosomal recessive nonsyndromic deafness 68

SLC44A2 [ENSP00000336888]

Solute carrier family 44 (choline transporter), member 2; Isoform 1, but not isoform 3, exhibits some choline transporter activity; Solute carriers

Synonyms:  SLC44A2,  SLC44A2p,  hSLC44A2,  B3KX31,  K7EMR2 ...

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.