Myelin P2 protein

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Myelin P2 protein also peripheral myelin protein 2, is a protein that in humans is encoded by the PMP2 gene.[5][6][7] Myelin protein P2 is a constituent of peripheral nervous system (PNS) myelin, also present in small amounts in central nervous system (CNS) myelin. As a structural protein, P2 is thought to stabilize the myelin membranes, and may play a role in lipid transport in Schwann cells. Structurally, P2 belongs to the family of cytoplasmic fatty acid-binding proteins (FABPs).

PDBOrtholog search: PDBe RCSB
AliasesPMP2, FABP8, M-FABP, MP2, P2, peripheral myelin protein 2, Myelin P2 protein, CMT1G
Quick facts PMP2, Available structures ...
PMP2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPMP2, FABP8, M-FABP, MP2, P2, peripheral myelin protein 2, Myelin P2 protein, CMT1G
External IDsOMIM: 170715; MGI: 102667; HomoloGene: 20589; GeneCards: PMP2; OMA:PMP2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002677
NM_001348381

NM_001030305

RefSeq (protein)

NP_002668
NP_001335310

NP_001025476

Location (UCSC)Chr 8: 81.44 – 81.45 MbChr 3: 10.24 – 10.25 Mb
PubMed search[3][4]
Wikidata
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