DISEASES

Disease-gene associations mined from literature

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Literature associating NIPA2 and chromosome 22q11.2 microduplication syndrome

NIPA2 [ENSP00000337618]

Non-imprinted in Prader-Willi/Angelman syndrome region protein 2; Acts as a selective Mg(2+) transporter; Belongs to the NIPA family.

Synonyms:  NIPA2,  NIPA2p,  hNIPA2,  A0A024R372,  H0YMQ7 ...

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.