DISEASES

Disease-gene associations mined from literature

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Literature associating PROX2 and atrial heart septal defect 6

PROX2 [ENSP00000451223]

Prospero homeobox protein 2; Transcription regulator. Does not seem to be essential for embryonic development and postnatal survival (By similarity). ; Belongs to the Prospero homeodomain family.

Synonyms:  PROX2,  PROX2p,  hPROX2,  A0A0G2JMC2,  G3V3G0 ...

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.