SLC46A3

SLC46A3
Identifiers
Aliases	SLC46A3, FKSG16, SLC46A3 (gene), solute carrier family 46 member 3
External IDs	OMIM: 616764; MGI: 1918956; HomoloGene: 41733; GeneCards: SLC46A3; OMA:SLC46A3 - orthologs
Gene location (Human)
Chr.	Chromosome 13 (human)
End	28,718,970 bp
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)
End	147,831,625 bp
RNA expression pattern
	Top expressed in
	mucosa of ileum; ; jejunal mucosa; ; Epithelium of choroid plexus; ; right lobe of liver; ; duodenum; ; mucosa of transverse colon; ; gallbladder; ; glomerulus; ; kidney tubule; ; dorsal motor nucleus of vagus nerve;
	Top expressed in
	epithelium of small intestine; ; lacrimal gland; ; ileum; ; jejunum; ; salivary gland; ; parotid gland; ; right kidney; ; left lobe of liver; ; olfactory epithelium; ; spleen;
	More reference expression data
	n/a
Gene ontology
Molecular function	molecular function;
Cellular component	integral component of membrane; extracellular exosome; membrane;
Biological process	transmembrane transport; biological process;
	Sources:Amigo / QuickGO
Orthologs
	283537
	71706
	ENSG00000139508
	ENSMUSG00000029650
	Q7Z3Q1
	Q9DC26
	NM_001135919; NM_181785; NM_001347960
	NM_027872; NM_001357002
	NP_001129391; NP_861450; NP_001334889
	NP_082148; NP_001343931
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 46, member 3 is a protein that in humans is encoded by the SLC46A3 gene.^[5]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000139508 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000029650 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Entrez Gene: Solute carrier family 46, member 3".

Chalasani N, Guo X, Loomba R, Goodarzi MO, Haritunians T, Kwon S, Cui J, Taylor KD, Wilson L, Cummings OW, Chen YD, Rotter JI (Nov 2010). "Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease". Gastroenterology. 139 (5): 1567–76, 1576.e1–6. doi:10.1053/j.gastro.2010.07.057. PMC 2967576. PMID 20708005.
Ma Y, Qi X, Du J, Song S, Feng D, Qi J, Zhu Z, Zhang X, Xiao H, Han Z, Hao X (2009). "Identification of candidate genes for human pituitary development by EST analysis". BMC Genomics. 10: 109. doi:10.1186/1471-2164-10-109. PMC 2664823. PMID 19284880.{{cite journal}}: CS1 maint: unflagged free DOI (link)

This article on a gene on human chromosome 13 is a stub. You can help Wikipedia by expanding it.