Probable low affinity copper uptake protein 2

SLC31A2
Identifiers
Aliases	SLC31A2, COPT2, CTR2, hCTR2, solute carrier family 31 member 2
External IDs	OMIM: 603088; MGI: 1333844; HomoloGene: 37536; GeneCards: SLC31A2; OMA:SLC31A2 - orthologs
Gene location (Human)
Chr.	Chromosome 9 (human)
End	113,164,140 bp
Gene location (Mouse)
Chr.	Chromosome 4 (mouse)
End	62,216,648 bp
RNA expression pattern
	Top expressed in
	parotid gland; ; inferior ganglion of vagus nerve; ; C1 segment; ; corpus callosum; ; Pons; ; subthalamic nucleus; ; Medulla Oblongata; ; monocyte; ; superior vestibular nucleus; ; decidua;
	Top expressed in
	lacrimal gland; ; seminal vesicula; ; parotid gland; ; neural layer of retina; ; granulocyte; ; spermatid; ; submandibular gland; ; renal corpuscle; ; lip; ; gastrula;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	copper ion transmembrane transporter activity;
Cellular component	integral component of membrane; recycling endosome; late endosome; integral component of plasma membrane; membrane; plasma membrane;
Biological process	copper ion transport; ion transport; copper ion transmembrane transport; regulation of copper ion transmembrane transport; cellular copper ion homeostasis;
	Sources:Amigo / QuickGO
Orthologs
	1318
	20530
	ENSG00000136867
	ENSMUSG00000066152
	O15432
	Q9CPU9
	NM_001860
	NM_001290518; NM_025286
	NP_001851
	NP_001277447; NP_079562
	Wikidata
View/Edit Human	View/Edit Mouse

Probable low affinity copper uptake protein 2 is a protein that in humans is encoded by the SLC31A2 gene.