GC and CUBN

Number of citations of the paper that reports this interaction (PMID 11717447)
41

Data Source:
HPRD (in vivo, in vitro)

		GC	CUBN
Gene Name		group-specific component (vitamin D binding protein)	cubilin (intrinsic factor-cobalamin receptor)
Image
Gene Ontology Annotations	Cellular Component	Extracellular Region Extracellular Space Cytosol Lysosomal Lumen Extracellular Vesicular Exosome Blood Microparticle	Lysosomal Membrane Endoplasmic Reticulum Golgi Apparatus Cytosol Plasma Membrane Coated Pit Endosome Membrane Membrane Apical Plasma Membrane Endocytic Vesicle Extrinsic Component Of External Side Of Plasma Membrane Brush Border Membrane Lysosomal Lumen Extracellular Vesicular Exosome
	Molecular Function	Actin Binding Vitamin D Binding Vitamin Transporter Activity Calcidiol Binding	Receptor Activity Transporter Activity Calcium Ion Binding Protein Binding Cobalamin Binding Protein Homodimerization Activity
	Biological Process	Steroid Metabolic Process Vitamin D Metabolic Process Small Molecule Metabolic Process Vitamin Transport	Tissue Homeostasis Vitamin Metabolic Process Water-soluble Vitamin Metabolic Process Receptor-mediated Endocytosis Steroid Metabolic Process Cholesterol Metabolic Process Cobalamin Metabolic Process Cobalamin Transport Lipoprotein Metabolic Process Vitamin D Metabolic Process Lipoprotein Transport Small Molecule Metabolic Process
Pathways		Metabolism of lipids and lipoproteins Metabolism of steroid hormones and vitamin D Vitamin D (calciferol) metabolism	Lipoprotein metabolism Metabolism of vitamins and cofactors Defective CD320 causes methylmalonic aciduria Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF Metabolism of lipids and lipoproteins Defective BTD causes biotidinase deficiency Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC Defective MTR causes methylmalonic aciduria and homocystinuria type cblG Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE Defective AMN causes hereditary megaloblastic anemia 1 Defects in cobalamin (B12) metabolism Defective GIF causes intrinsic factor deficiency Defective HLCS causes multiple carboxylase deficiency Defective MMAB causes methylmalonic aciduria type cblB Lipid digestion, mobilization, and transport Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD Metabolism of steroid hormones and vitamin D Defective MMAA causes methylmalonic aciduria type cblA Defective CUBN causes hereditary megaloblastic anemia 1 Cobalamin (Cbl, vitamin B12) transport and metabolism HDL-mediated lipid transport 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 Vitamin D (calciferol) metabolism Defects in vitamin and cofactor metabolism
Drugs			Hydroxocobalamin
Diseases
GWAS		Metabolite levels ( 22916037) Non-alcoholic fatty liver disease histology (other) ( 23213074) Vitamin D insufficiency ( 20541252) Vitamin D levels ( 22673963 20418485)	Folate pathway vitamin levels ( 19303062 19744961) MRI atrophy measures ( 21116278) Quantitative traits ( 19197348) Urinary albumin excretion ( 21355061)
Protein-Protein Interactions		12 interactors: ACTA1 ACTA2 ACTC1 C3 CCND3 CDC73 CUBN GRB2 LRIF1 LRP2 PIK3R3 SERF2	9 interactors: ALB BRCA1 CBL GC GIF LGALS3 LRP2 SCGB1A1 TF
Entrez ID		2638	8029
HPRD ID		00749	04296
Ensembl ID		ENSG00000145321	ENSG00000107611
Uniprot IDs		P02774	O60494
PDB IDs		1J78 1J7E 1KW2 1KXP 1LOT 1MA9	3KQ4
Enriched GO Terms of Interacting Partners?		Skeletal Muscle Thin Filament Assembly Skeletal Myofibril Assembly Vitamin D Metabolic Process Actin-myosin Filament Sliding Muscle Filament Sliding Muscle Contraction Actin-mediated Cell Contraction Muscle System Process Actin Filament-based Movement Receptor-mediated Endocytosis Myofibril Assembly Tissue Development Skeletal Muscle Fiber Adaptation Positive Regulation Of Type IIa Hypersensitivity Cell Development Response To External Stimulus Anatomical Structure Formation Involved In Morphogenesis Actomyosin Structure Organization Vitamin Metabolic Process Positive Regulation Of Activation Of Membrane Attack Complex Insulin Receptor Signaling Pathway Striated Muscle Cell Development Lipid Metabolic Process Glomerular Mesangial Cell Development Regulation Of Phosphorylation Muscle Cell Development Cobalamin Transport Mesangial Cell Development Positive Regulation Of Hypersensitivity Endocytosis Renal Interstitial Fibroblast Development Positive Regulation Of Apoptotic Cell Clearance Positive Regulation Of Acute Inflammatory Response To Antigenic Stimulus Histone H2B Ubiquitination Skeletal Muscle Adaptation Response To Stimulus Regulation Of Phosphorus Metabolic Process Cellular Response To Insulin Stimulus	Vitamin Metabolic Process Vitamin D Metabolic Process Steroid Metabolic Process Vitamin Transport Regulation Of Extrinsic Apoptotic Signaling Pathway Via Death Domain Receptors Retina Homeostasis Negative Regulation Of Apoptotic Process Negative Regulation Of Programmed Cell Death Negative Regulation Of Cell Death Platelet Degranulation Positive Regulation Of Histone H4-K20 Methylation Negative Regulation Of Immunological Synapse Formation Positive Regulation Of Histone H4-K16 Acetylation Blood Coagulation Hemostasis Negative Regulation Of Signal Transduction Response To Stress Negative Regulation Of T Cell Activation Response To Steroid Hormone Negative Regulation Of Signaling Negative Regulation Of Leukocyte Cell-cell Adhesion Cellular Response To Tumor Necrosis Factor Negative Regulation Of Homotypic Cell-cell Adhesion Positive Regulation Of Histone H3-K9 Acetylation Glucosylceramide Catabolic Process Maintenance Of Mitochondrion Location Negative Regulation Of T Cell Activation Via T Cell Receptor Contact With Antigen Bound To MHC Molecule On Antigen Presenting Cell Small Molecule Metabolic Process Lipid Metabolic Process Regulation Of Cytokine Production Response To Tumor Necrosis Factor Regulation Of Body Fluid Levels Negative Regulation Of Extrinsic Apoptotic Signaling Pathway Response To Platinum Ion Hemolysis By Symbiont Of Host Erythrocytes Positive Regulation Of Circadian Sleep/wake Cycle, Non-REM Sleep Positive Regulation Of Histone H4 Acetylation Negative Regulation Of Histone H3-K4 Methylation Positive Regulation Of Mononuclear Cell Migration Response To Silicon Dioxide Negative Regulation Of Lymphocyte Activation Negative Regulation Of Cell-cell Adhesion Response To Organic Substance Wound Healing Response To Stimulus Regulation Of T Cell Proliferation Regulation Of Apoptotic Process Mononuclear Cell Migration Response To Glucocorticoid Negative Regulation Of Leukocyte Activation
Tagcloud ?		absent agglutinin bcr bm centers centroblasts centrocytes chimeric clusters fdc follicles follicular gcs germinal grafts hosts humoral lt ltbeta ltbetar lymphotoxin networks peanut pna radioresistant reciprocal reconstituted splenic tnfrp55	accordingly advocate amn amnionless b12 coexpressed coreceptor correct critically cubilin endocytosis extremely glomerular ileum interdependency internalization lacks localize lrp2 malabsorption megalin mutually proteinuria suffer surprisingly transmembrane tubules ultrafiltrate vitamin
Tagcloud (Difference) ?		absent agglutinin bcr bm centers centroblasts centrocytes chimeric clusters fdc follicles follicular gcs germinal grafts hosts humoral lt ltbeta ltbetar lymphotoxin networks peanut pna radioresistant reciprocal reconstituted splenic tnfrp55	accordingly advocate amn amnionless b12 coexpressed coreceptor correct critically cubilin endocytosis extremely glomerular ileum interdependency internalization lacks localize lrp2 malabsorption megalin mutually proteinuria suffer surprisingly transmembrane tubules ultrafiltrate vitamin
Tagcloud (Intersection) ?