DISEASES

Disease-gene associations mined from literature

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Literature associating KCTD2 and myoclonic dystonia

KCTD2 [ENSP00000312814]

BTB/POZ domain-containing protein KCTD2; Potassium channel tetramerization domain containing 2

Synonyms:  KCTD2,  KCTD2p,  hKCTD2,  H0Y3B9,  J3QSC8 ...

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.