SLC2A1 and SNX27

Number of citations of the paper that reports this interaction (PubMedID 29117568)
7

Data Source:
BioGRID (pull down)

		SLC2A1	SNX27
Description		solute carrier family 2 member 1	sorting nexin 27
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GO Annotations	Cellular Component	Golgi Membrane Female Pronucleus Cytosol Plasma Membrane Integral Component Of Plasma Membrane Caveola Intercalated Disc Membrane Basolateral Plasma Membrane Apical Plasma Membrane Z Disc Midbody Cortical Actin Cytoskeleton Sarcolemma Melanosome Extracellular Exosome Blood Microparticle Presynapse	Immunological Synapse Nucleoplasm Endosome Early Endosome Cytosol Retromer Complex Early Endosome Membrane WASH Complex
	Molecular Function	Glucose Transmembrane Transporter Activity Protein Binding Kinase Binding Dehydroascorbic Acid Transmembrane Transporter Activity Identical Protein Binding Xenobiotic Transmembrane Transporter Activity Protein Self-association D-glucose Transmembrane Transporter Activity	Protein Binding Phosphatidylinositol-3-phosphate Binding Phosphatidylinositol Binding
	Biological Process	Response To Hypoxia Lactose Biosynthetic Process Female Pregnancy Regulation Of Glucose Transmembrane Transport L-ascorbic Acid Metabolic Process Cerebral Cortex Development Response To Insulin Cellular Response To Glucose Starvation Xenobiotic Transport Regulation Of Insulin Secretion Protein-containing Complex Assembly Dehydroascorbic Acid Transport Cellular Response To Mechanical Stimulus Cellular Hyperosmotic Response Response To Thyroglobulin Triiodothyronine Glucose Transmembrane Transport	Establishment Of Natural Killer Cell Polarity Intracellular Protein Transport Signal Transduction Endosome To Lysosome Transport Endosomal Transport Retrograde Transport, Endosome To Plasma Membrane
Pathways		Cellular hexose transport Vitamin C (ascorbate) metabolism Regulation of insulin secretion Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1) Lactose synthesis
Drugs		Resveratrol
Diseases		GLUT1 deficiency syndrome (GLUT1DS); Glucose transport defect of the blood-brain barrier Primary torsion dystonia (PTD)
GWAS		Birth weight ( 31043758) Cardiac hypertrophy ( 21348951) Monocyte count ( 27863252) Pre-treatment viral load in HIV-1 infection ( 31219150)	Body mass index ( 26426971)
Interacting Genes		13 interacting genes: CALR CANX COPS6 GAPDH GIPC1 HSPB2 PDIA3 PTK2B SNX27 STOM SUMO1 UBE2I VHL	10 interacting genes: AKT2 APP DGKZ HLCS PNPLA3 PTEN RPS6KA1 SELP SLC2A1 VPS26A
Entrez ID		6513	81609
HPRD ID		00683	11591
Ensembl ID		ENSG00000117394	ENSG00000143376
Uniprot IDs		P11166 Q59GX2	A0A2R8Y8A7 Q96L92
PDB IDs		1SUK 4PYP 5EQG 5EQH 5EQI	4HAS 5ZN9 6SAK
Enriched GO Terms of Interacting Partners?
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