DISEASES

Disease-gene associations mined from literature

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Literature associating KCTD1 and branchiooculofacial syndrome

KCTD1 [ENSP00000384367]

Potassium channel tetramerization domain-containing protein 1; May repress the transcriptional activity of AP-2 family members, including TFAP2A, TFAP2B and TFAP2C to various extent.

Synonyms:  KCTD1,  KCTD1p,  hKCTD1,  A0A024RC45,  J3KSG1 ...

Linkouts:  STRING  Pharos  UniProt

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.