SLC66A3

SLC66A3
Identifiers
Aliases	SLC66A3, C2orf22, PQ loop repeat containing 3, solute carrier family 66 member 3, PQLC3
External IDs	MGI: 2444067; HomoloGene: 16454; GeneCards: SLC66A3; OMA:SLC66A3 - orthologs
Gene location (Human)
Chr.	Chromosome 2 (human)
End	11,178,870 bp
Gene location (Mouse)
Chr.	Chromosome 12 (mouse)
End	17,050,409 bp
RNA expression pattern
	Top expressed in
	oocyte; ; secondary oocyte; ; gonad; ; monocyte; ; skin of arm; ; synovial membrane; ; decidua; ; germinal epithelium; ; Achilles tendon; ; corpus epididymis;
	Top expressed in
	olfactory epithelium; ; granulocyte; ; corneal stroma; ; lumbar spinal ganglion; ; choroid plexus of fourth ventricle; ; stroma of bone marrow; ; mucous cell of stomach; ; Ileal epithelium; ; decidua; ; carotid body;
	More reference expression data
	n/a
Orthologs
	130814
	217430
	ENSG00000162976
	ENSMUSG00000045679
	Q8N755
	Q8C6U2
	NM_001282710; NM_001282711; NM_001282712; NM_152391
	NM_001161111; NM_172574
	NP_001269639; NP_001269640; NP_001269641; NP_689604
	NP_766162
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 66 member 3 is a gene in humans that encodes the protein SLC66A3. The function of the SLC66A3 protein is not yet well understood but belongs to a family of five evolutionarily related proteins, the SLC66 lysosomal amino acid transporters. SLC66A3 is localized to the endoplasmic reticulum and has four transmembrane domains.