SLC29A3

Description		solute carrier family 29 member 3
Image		No pdb structure
GO Annotations	Cellular Component	Lysosomal Membrane Golgi Apparatus Plasma Membrane Integral Component Of Membrane Late Endosome Membrane Intracellular Membrane-bounded Organelle
	Molecular Function	Nucleoside Transmembrane Transporter Activity Protein Binding
	Biological Process	Nucleoside Transmembrane Transport
Pathways		Defective SLC29A3 causes histiocytosis-lymphadenopathy plus syndrome (HLAS) Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane
Drugs
Diseases		Hyperpigmentation, cutaneous, with hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, and hypogonadism; H syndrome
GWAS		Diisocyanate-induced asthma ( 25918132) Disease progression in age-related macular degeneration (adjusted for baseline) ( 29346644) Lymphocyte counts ( 32888494) Monocyte count ( 32888494) Obesity-related traits ( 23251661) Sleep duration ( 30531941) Systemic lupus erythematosus ( 23273568) Vitiligo ( 22951725) White blood cell count ( 32888494)
Interacting Genes		1 interacting genes: CREB3
Entrez ID		55315
HPRD ID		11570
Ensembl ID		ENSG00000198246
Uniprot IDs		Q9BZD2
PDB IDs
Enriched GO Terms of Interacting Partners?
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