Slc18a2

Predicted to enable several functions, including amine transmembrane transporter activity; heat shock protein binding activity; and monoamine transmembrane transporter activity. Involved in histamine secretion by mast cell; neurotransmitter loading into synaptic vesicle; and serotonin secretion by mast cell. Acts upstream of or within several processes, including locomotory behavior; response to amphetamine; and response to toxic substance. Located in synaptic vesicle membrane. Is active in dopaminergic synapse. Is expressed in several structures, including adrenal gland; alimentary system; blastocyst; brain; and eye. Human ortholog(s) of this gene implicated in Parkinson's disease; infantile parkinsonism-dystonia 2; and type 1 diabetes mellitus. Orthologous to human SLC18A2 (solute carrier family 18 member A2). [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 mouse Slc18a2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.

Biological processes and signaling networks where the Slc18a2 gene in mouse plays a role, providing insight into its function and relevance in health or disease.

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.

Describes the biological processes, cellular components, and molecular functions associated with the mouse Slc18a2 gene, providing context for its role in the cell.