Pmp2 Gene Summary [Mouse]

Predicted to enable cholesterol binding activity and fatty acid binding activity. Acts upstream of or within membrane organization. Predicted to be located in cytoplasm and myelin sheath. Predicted to be active in cytosol and nucleus. Human ortholog(s) of this gene implicated in Charcot-Marie-Tooth disease type 1G. Orthologous to human PMP2 (peripheral myelin protein 2). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Pmp2
Official Name
peripheral myelin protein 2 [Source:MGI Symbol;Acc:MGI:102667]
Ensembl ID
ENSMUSG00000052468
Bio databases IDs NCBI: 18857 Ensembl: ENSMUSG00000052468
Aliases peripheral myelin protein 2
Synonyms P2, peripheral myelin protein 2
Species
Mouse, Mus musculus

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in mouse Pmp2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • cholesterol binding
  • lipocalin/cytosolic fatty acid-binding protein family
  • fatty acid binding
  • Lipocalin / cytosolic fatty-acid binding protein family

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
binds
regulated by
role in cell
  • organization

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Unknown

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.