B4GALT1 and OR10G4

Data Source:
BioGRID (two hybrid)

		B4GALT1	OR10G4
Description		beta-1,4-galactosyltransferase 1	olfactory receptor family 10 subfamily G member 4
Image			No pdb structure
GO Annotations	Cellular Component	Golgi Trans Cisterna Golgi Membrane Extracellular Space Golgi Apparatus Plasma Membrane External Side Of Plasma Membrane Membrane Integral Component Of Membrane Basolateral Plasma Membrane Desmosome Filopodium Secretory Granule Membrane Brush Border Membrane Golgi Cisterna Membrane Azurophil Granule Membrane Extracellular Exosome	Plasma Membrane Integral Component Of Membrane
	Molecular Function	Beta-N-acetylglucosaminylglycopeptide Beta-1,4-galactosyltransferase Activity N-acetyllactosamine Synthase Activity Lactose Synthase Activity Cytoskeletal Protein Binding Galactosyltransferase Activity Manganese Ion Binding UDP-galactosyltransferase Activity	G Protein-coupled Receptor Activity Olfactory Receptor Activity Protein Binding
	Biological Process	Epithelial Cell Development Acute Inflammatory Response Lactose Biosynthetic Process Galactose Metabolic Process Protein N-linked Glycosylation Cell Adhesion Binding Of Sperm To Zona Pellucida Penetration Of Zona Pellucida Negative Regulation Of Cell Population Proliferation Oligosaccharide Biosynthetic Process Keratan Sulfate Biosynthetic Process Extracellular Matrix Organization Positive Regulation Of Apoptotic Process Neutrophil Degranulation Development Of Secondary Sexual Characteristics Leukocyte Migration Regulation Of Acrosome Reaction Positive Regulation Of Epithelial Cell Proliferation Involved In Wound Healing Angiogenesis Involved In Wound Healing Glycosylation	G Protein-coupled Receptor Signaling Pathway Detection Of Chemical Stimulus Involved In Sensory Perception Of Smell
Pathways		Pre-NOTCH Processing in Golgi Keratan sulfate biosynthesis Interaction With Cumulus Cells And The Zona Pellucida Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Lactose synthesis Neutrophil degranulation N-Glycan antennae elongation	Olfactory Signaling Pathway
Drugs		N-Acetylglucosamine 6-Aminohexyl-uridine-C1,5'-diphosphate 4)-N-acetyl-beta-D-glucosamine Galactose-uridine-5'-diphosphate Uridine monophosphate 2-(N-morpholino)ethanesulfonic acid
Diseases		Congenital disorders of glycosylation (CDG) type II
GWAS		Aspartate aminotransferase levels ( 29403010) Blood protein levels ( 30072576 29875488) Hematocrit ( 32888494) Hemoglobin ( 32888494) IgG fucosylation phenotypes (multivariate analysis) ( 28878392) IgG galactosylation phenotypes (multivariate analysis) ( 28878392) IgG glycosylation ( 23382691) IgG N-glycosylation phenotypes (multivariate analysis) ( 28878392 32128391) Influenza A (H1N1) infection ( 26379185) Mild influenza (H1N1) infection ( 26379185) N-glycan levels ( 31163085) Red blood cell count ( 32888494) Serum uric acid levels ( 30993211) Severe influenza A (H1N1) infection ( 26379185) Urate levels ( 31985003 31578528 23263486)
Interacting Genes		8 interacting genes: CDK11A EGFR LALBA OR10G4 TFRC TUBA1A TUBA4A TUBB	2 interacting genes: B4GALT1 RPL12
Entrez ID		2683	390264
HPRD ID		00659	14889
Ensembl ID		ENSG00000086062	ENSG00000254737
Uniprot IDs		P15291	A0A126GWS5 Q8NGN3
PDB IDs		2AE7 2AEC 2AES 2AGD 2AH9 2FY7 2FYA 2FYB 3EE5 4EE3 4EE4 4EE5 4EEA 4EEG 4EEM 4EEO 4L41 6FWT 6FWU
Enriched GO Terms of Interacting Partners?
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