DISEASES

Disease-gene associations mined from literature

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Literature associating PMP22 and Charcot-Marie-Tooth disease type 1D

PMP22 [ENSP00000484631]

Growth arrest-specific protein 3; Might be involved in growth regulation, and in myelinization in the peripheral nervous system; Belongs to the PMP-22/EMP/MP20 family.

Synonyms:  PMP22,  PMP22p,  hPMP22,  A8MU75,  B4DUL1 ...

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.