SLC5A6 and GALNT6

Number of citations of the paper that reports this interaction (PMID 21988832)
14

Data Source:
BioGRID (two hybrid)

		SLC5A6	GALNT6
Gene Name		solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6	polypeptide N-acetylgalactosaminyltransferase 6
Image		No pdb structure	No pdb structure
Gene Ontology Annotations	Cellular Component	Plasma Membrane Integral Component Of Plasma Membrane Vesicle Membrane Membrane Brush Border Membrane	Golgi Membrane Golgi Apparatus Integral Component Of Membrane Perinuclear Region Of Cytoplasm
	Molecular Function	Sodium-dependent Multivitamin Transmembrane Transporter Activity	Polypeptide N-acetylgalactosaminyltransferase Activity Carbohydrate Binding Metal Ion Binding
	Biological Process	Vitamin Metabolic Process Water-soluble Vitamin Metabolic Process Biotin Metabolic Process Transport Sodium Ion Transport Biotin Transport Pantothenate Transmembrane Transport Pantothenate Metabolic Process Small Molecule Metabolic Process Transmembrane Transport	Protein O-linked Glycosylation O-glycan Processing Post-translational Protein Modification Cellular Protein Metabolic Process
Pathways		Metabolism of vitamins and cofactors Defective CD320 causes methylmalonic aciduria Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF Defective BTD causes biotidinase deficiency Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC Defective MTR causes methylmalonic aciduria and homocystinuria type cblG SLC-mediated transmembrane transport Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE Defective AMN causes hereditary megaloblastic anemia 1 Transport of vitamins, nucleosides, and related molecules Defects in cobalamin (B12) metabolism Defective GIF causes intrinsic factor deficiency Vitamin B5 (pantothenate) metabolism Defective HLCS causes multiple carboxylase deficiency Defective MMAB causes methylmalonic aciduria type cblB Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD Defective MMAA causes methylmalonic aciduria type cblA Defective CUBN causes hereditary megaloblastic anemia 1 Defective MUT causes methylmalonic aciduria mut type Metabolism of water-soluble vitamins and cofactors Defects in biotin (Btn) metabolism Defective TCN2 causes hereditary megaloblastic anemia Biotin transport and metabolism Defects in vitamin and cofactor metabolism	Post-translational protein modification O-linked glycosylation of mucins O-linked glycosylation
Drugs		Biotin Lipoic Acid
Diseases
GWAS
Protein-Protein Interactions		2 interactors: ERBB2IP GALNT6	5 interactors: ALDOA FN1 SLC5A6 TAF9 TMEM9
Entrez ID		8884	11226
HPRD ID		04934	05512
Ensembl ID		ENSG00000138074	ENSG00000139629
Uniprot IDs		Q9HD19 Q9Y289	Q8NCL4
PDB IDs
Enriched GO Terms of Interacting Partners?		Basal Protein Localization Establishment Or Maintenance Of Epithelial Cell Apical/basal Polarity Asymmetric Protein Localization Establishment Or Maintenance Of Apical/basal Cell Polarity Intermediate Filament Cytoskeleton Organization Intermediate Filament-based Process O-glycan Processing	Platelet Degranulation Pantothenate Transmembrane Transport Biotin Transport Positive Regulation Of Cell Growth Regulation Of Cell Shape Platelet Activation Fructose 1,6-bisphosphate Metabolic Process Calcium-independent Cell-matrix Adhesion Positive Regulation Of Growth Exocytosis Regulation Of Cell Growth Pantothenate Metabolic Process Integrin Activation Biotin Metabolic Process Negative Regulation Of Intrinsic Apoptotic Signaling Pathway In Response To DNA Damage By P53 Class Mediator Vitamin Transmembrane Transport Blood Coagulation Hemostasis Negative Regulation Of Intrinsic Apoptotic Signaling Pathway By P53 Class Mediator
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