MGP Database

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MGP000796

Ontology/Pathway Information

Entrez Gene ID1634
Gene Namedecorin
Gene Symbol DCN
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005589 IEA:EnsemblCcollagen type VI trimer
GO:0005576 TAS:ReactomeCextracellular region
GO:0005615 IDA:BHF-UCLCextracellular space
GO:0005796 TAS:ReactomeCGolgi lumen
GO:0043202 TAS:ReactomeClysosomal lumen
GO:0005578 IEA:UniProtKB-SubCellCproteinaceous extracellular matrix
GO:0050840 IEA:EnsemblFextracellular matrix binding
GO:0005539 IEA:EnsemblFglycosaminoglycan binding
GO:0044822 IDA:UniProtKBFpoly(A) RNA binding
GO:0007568 IEA:EnsemblPaging
GO:0005975 TAS:ReactomePcarbohydrate metabolic process
GO:0030206 TAS:ReactomePchondroitin sulfate biosynthetic process
GO:0030207 TAS:ReactomePchondroitin sulfate catabolic process
GO:0030204 TAS:ReactomePchondroitin sulfate metabolic process
GO:0030208 TAS:ReactomePdermatan sulfate biosynthetic process
GO:0022617 TAS:ReactomePextracellular matrix disassembly
GO:0030198 TAS:ReactomePextracellular matrix organization
GO:0030203 TAS:ReactomePglycosaminoglycan metabolic process
GO:0001822 IEA:EnsemblPkidney development
GO:0009887 TAS:ProtIncPorgan morphogenesis
GO:0019800 IEA:EnsemblPpeptide cross-linking via chondroitin 4-sulfate glycosaminoglycan
GO:0001890 IEA:EnsemblPplacenta development
GO:0032496 IEA:EnsemblPresponse to lipopolysaccharide
GO:0009612 IEA:EnsemblPresponse to mechanical stimulus
GO:0007519 IEA:EnsemblPskeletal muscle tissue development
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0042060 IEA:EnsemblPwound healing
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_121408A tetrasaccharide linker sequence is required for GAG synthesis
REACT_120989Chondroitin sulfate biosynthesis
REACT_121206Chondroitin sulfate/dermatan sulfate metabolism
REACT_120888CS/DS degradation
REACT_268678Defective B3GAT3 causes JDSSDHD
REACT_268431Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
REACT_268749Defective B4GALT7 causes EDS, progeroid type
REACT_267917Defective CHST14 causes EDS, musculocontractural type
REACT_267648Defective CHST3 causes SEDCJD
REACT_268786Defective CHST6 causes MCDC1
REACT_268113Defective CHSY1 causes TPBS
REACT_267942Defective EXT1 causes exostoses 1, TRPS2 and CHDS
REACT_267741Defective EXT2 causes exostoses 2
REACT_268843Defective PAPSS2 causes SEMD-PA
REACT_268059Defective SLC26A2 causes chondrodysplasias
REACT_118572Degradation of the extracellular matrix
REACT_120800Dermatan sulfate biosynthesis
REACT_116125Disease
REACT_268624Diseases associated with glycosaminoglycan metabolism
REACT_268324Diseases of glycosylation
REACT_163906ECM proteoglycans
REACT_118779Extracellular matrix organization
REACT_264090Glycogen storage diseases
REACT_121315Glycosaminoglycan metabolism
REACT_121314Heparan sulfate/heparin (HS-GAG) metabolism
REACT_111217Metabolism
REACT_474Metabolism of carbohydrates
REACT_147857MPS I - Hurler syndrome
REACT_147734MPS II - Hunter syndrome
REACT_147753MPS IIIA - Sanfilippo syndrome A
REACT_147788MPS IIIB - Sanfilippo syndrome B
REACT_147860MPS IIIC - Sanfilippo syndrome C
REACT_147749MPS IIID - Sanfilippo syndrome D
REACT_147825MPS IV - Morquio syndrome A
REACT_147798MPS IV - Morquio syndrome B
REACT_147739MPS IX - Natowicz syndrome
REACT_147759MPS VII - Sly syndrome
REACT_147719MPS VI - Maroteaux-Lamy syndrome
REACT_147853Mucopolysaccharidoses
REACT_264430Myoclonic epilepsy of Lafora
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