PMP22

Gene Information
  • Official Symbol: PMP22
  • Official Name: peripheral myelin protein 22
  • Aliases and Previous Symbols: N/A
  • Entrez ID: 5376
  • UniProt: Q01453
  • Interactions: BioGRID
  • PubMed articles: Open PubMed
  • OMIM: Open OMIM
Function Summary
  • Entrez Summary: This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013].
  • UniProt Summary: Might be involved in growth regulation, and in myelinization in the peripheral nervous system.

Pfam Domains GO Terms


CRISPR Data

Compound Hit Most Correlated Genes in Chemogenomics Tissues where Essential in the Avana Dataset (DepMap 20Q1)

Essentiality in NALM6
  • Essentiality Rank: 18160
  • Expression level (log2 read counts): 4.11

Expression Distribution

  • Last modified: 2026/01/07 22:36
  • by 127.0.0.1