DISEASES

Disease-gene associations mined from literature

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Literature associating PIGT and multiple congenital anomalies-hypotonia-seizures syndrome

PIGT [ENSP00000279036]

GPI transamidase component PIG-T; Component of the GPI transamidase complex. Essential for transfer of GPI to proteins, particularly for formation of carbonyl intermediates.

Synonyms:  PIGT,  A0A1W2PNP0,  A0A1W2PNS2,  A0A1W2PNW9,  A0A1W2PNZ5 ...

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.