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Involved in axon ensheathment and nerve development. Predicted to be located in cytosol; nuclear speck; and plasma membrane. Predicted to be active in cytoplasm and nucleus. Human ortholog(s) of this gene implicated in Charcot-Marie-Tooth disease type 3 and Charcot-Marie-Tooth disease type 4F. Orthologous to human PRX (periaxin). [provided by Alliance of Genome Resources, Jul 2025]
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 rat Prx often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
Domain present in PSD-95, Dlg, and ZO-1/2
Cornifin (SPRR) family
canonical PDZ domain
protein binding
PDZ domain
basic domain
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
Nucleus
Cytoplasm
Plasma Membrane
cytosol
nuclear speckles
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the rat Prx gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
regulation of RNA splicing
axon ensheathment
peripheral nervous system myelin maintenance
Cellular Component
Where in the cell the gene product is active
nucleus
anchoring junction
cytoplasm
plasma membrane
Molecular Function
What the gene product does at the molecular level
protein binding
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.