DISEASES

Disease-gene associations mined from literature

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Literature associating MPDU1 and complex partial epilepsy

MPDU1 [ENSP00000250124]

Suppressor of Lec15 and Lec35 glycosylation mutation homolog; Required for normal utilization of mannose-dolichol phosphate (Dol-P-Man) in the synthesis of N-linked and O-linked oligosaccharides and GPI anchors; Belongs to the MPDU1 (TC 2.A.43.3) family.

Synonyms:  MPDU1,  MPDU1p,  hMPDU1,  B4DT74,  HBEBP2BPA ...

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.