SNX27 and SLC2A1

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

Data Source:
BioGRID (pull down)

		SNX27	SLC2A1
Description		sorting nexin 27	solute carrier family 2 member 1
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GO Annotations	Cellular Component	Immunological Synapse Nucleoplasm Endosome Early Endosome Cytosol Retromer Complex Early Endosome Membrane WASH Complex	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
	Molecular Function	Protein Binding Phosphatidylinositol-3-phosphate Binding Phosphatidylinositol Binding	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
	Biological Process	Establishment Of Natural Killer Cell Polarity Intracellular Protein Transport Signal Transduction Endosome To Lysosome Transport Endosomal Transport Retrograde Transport, Endosome To Plasma Membrane	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
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		Body mass index ( 26426971)	Birth weight ( 31043758) Cardiac hypertrophy ( 21348951) Monocyte count ( 27863252) Pre-treatment viral load in HIV-1 infection ( 31219150)
Interacting Genes		10 interacting genes: AKT2 APP DGKZ HLCS PNPLA3 PTEN RPS6KA1 SELP SLC2A1 VPS26A	13 interacting genes: CALR CANX COPS6 GAPDH GIPC1 HSPB2 PDIA3 PTK2B SNX27 STOM SUMO1 UBE2I VHL
Entrez ID		81609	6513
HPRD ID		11591	00683
Ensembl ID		ENSG00000143376	ENSG00000117394
Uniprot IDs		A0A2R8Y8A7 Q96L92	P11166 Q59GX2
PDB IDs		4HAS 5ZN9 6SAK	1SUK 4PYP 5EQG 5EQH 5EQI
Enriched GO Terms of Interacting Partners?
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