SLC46A3

SLC46A3
Identifiers
Aliases	SLC46A3, FKSG16, SLC46A3 (gene), solute carrier family 46 member 3
External IDs	MGI: 1918956 HomoloGene: 41733 GeneCards: SLC46A3
Gene location (Human)
Chr.	Chromosome 13 (human)[1]
End	28,718,970 bp[1]
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)[2]
End	147,894,815 bp[2]
Gene ontology
Molecular function	• molecular function;
Cellular component	• integral component of membrane; • extracellular exosome; • membrane;
Biological process	• transmembrane transport;
	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

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.

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