CSPG5

Gene Name		chondroitin sulfate proteoglycan 5 (neuroglycan C)
Image		No pdb structure
Gene Ontology Annotations	Cellular Component	Extracellular Region Endoplasmic Reticulum Membrane Golgi Apparatus Golgi Lumen Integral Component Of Plasma Membrane Membrane Integral Component Of Membrane Golgi-associated Vesicle Membrane Lysosomal Lumen
	Molecular Function	Protein Binding Growth Factor Activity
	Biological Process	Carbohydrate Metabolic Process Nervous System Development Pathogenesis Glycosaminoglycan Metabolic Process Chondroitin Sulfate Metabolic Process Chondroitin Sulfate Biosynthetic Process Chondroitin Sulfate Catabolic Process Dermatan Sulfate Biosynthetic Process Axon Regeneration Regulation Of Growth Small Molecule Metabolic Process Intracellular Transport Regulation Of Synaptic Transmission
Pathways		MPS IIIB - Sanfilippo syndrome B Diseases of glycosylation Heparan sulfate/heparin (HS-GAG) metabolism Defective B4GALT7 causes EDS, progeroid type MPS I - Hurler syndrome MPS IX - Natowicz syndrome Chondroitin sulfate/dermatan sulfate metabolism CS/DS degradation Defective SLC26A2 causes chondrodysplasias Glycosaminoglycan metabolism Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Defective CHST14 causes EDS, musculocontractural type Defective PAPSS2 causes SEMD-PA MPS IIIA - Sanfilippo syndrome A Myoclonic epilepsy of Lafora Defective CHST6 causes MCDC1 Glycogen storage diseases MPS IIID - Sanfilippo syndrome D A tetrasaccharide linker sequence is required for GAG synthesis Chondroitin sulfate biosynthesis MPS IIIC - Sanfilippo syndrome C Diseases associated with glycosaminoglycan metabolism Mucopolysaccharidoses Defective EXT2 causes exostoses 2 MPS II - Hunter syndrome Defective B3GAT3 causes JDSSDHD Defective CHST3 causes SEDCJD Defective EXT1 causes exostoses 1, TRPS2 and CHDS MPS IV - Morquio syndrome A Dermatan sulfate biosynthesis Defective CHSY1 causes TPBS MPS IV - Morquio syndrome B MPS VII - Sly syndrome Metabolism of carbohydrates MPS VI - Maroteaux-Lamy syndrome
Drugs
Diseases
GWAS
Protein-protein Interactions		1 interactors: GOPC
Entrez ID		10675
HPRD ID		08423
Ensembl ID
Uniprot IDs		B7Z2E0 O95196
PDB IDs
Enriched GO Terms of Interacting Partners?		Cytoplasmic Sequestering Of CFTR Protein Negative Regulation Of Golgi To Plasma Membrane Protein Transport Regulation Of Golgi To Plasma Membrane Protein Transport Negative Regulation Of Establishment Of Protein Localization To Plasma Membrane Apical Protein Localization Negative Regulation Of Protein Localization To Plasma Membrane Cytoplasmic Sequestering Of Protein Asymmetric Protein Localization Spermatid Nucleus Differentiation Golgi To Plasma Membrane Transport Regulation Of Establishment Of Protein Localization To Plasma Membrane Regulation Of Protein Localization To Plasma Membrane Post-Golgi Vesicle-mediated Transport Negative Regulation Of Intracellular Protein Transport ER To Golgi Vesicle-mediated Transport Negative Regulation Of Intracellular Transport Nucleus Organization Spermatid Development Maintenance Of Protein Location In Cell Spermatid Differentiation Maintenance Of Protein Location Maintenance Of Location In Cell Negative Regulation Of Protein Transport Germ Cell Development Protein Homooligomerization Regulation Of Intracellular Protein Transport Golgi Vesicle Transport Regulation Of Vesicle-mediated Transport Negative Regulation Of Transport Protein Oligomerization Regulation Of Intracellular Transport Spermatogenesis Male Gamete Generation
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