Homo sapiens Protein: DCN
Summary
InnateDB Protein IDBP-599721.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DCN
Protein Name decorin
Synonyms CSCD; DSPG2; PG40; PGII; PGS2; SLRR1B;
Species Homo sapiens
Ensembl Protein ENSP00000447674
InnateDB Gene IDBG-50872 (DCN)
Protein Structure
UniProt Annotation
Function May affect the rate of fibrils formation.
Subcellular Localization Secreted, extracellular space, extracellular matrix.
Disease Associations Corneal dystrophy, congenital stromal (CSCD) [MIM:610048]: A corneal dystrophy characterized by congenital corneal opacification consisting of a large number of flakes and spots throughout all layers of the stroma. It results in progressive, painless visual loss. Corneal erosions and photophobia are absent. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 25 experimentally validated interaction(s) in this database.
Experimentally validated
Total 25 [view]
Protein-Protein 24 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0005518 collagen binding
GO:0044822 poly(A) RNA binding
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0009887 organ morphogenesis
GO:0022617 extracellular matrix disassembly
GO:0030198 extracellular matrix organization
GO:0030203 glycosaminoglycan metabolic process
GO:0030204 chondroitin sulfate metabolic process
GO:0030206 chondroitin sulfate biosynthetic process
GO:0030207 chondroitin sulfate catabolic process
GO:0030208 dermatan sulfate biosynthetic process
GO:0044281 small molecule metabolic process
GO:0045087 innate immune response (InnateDB)
Cellular Component
GO:0005576 extracellular region
GO:0005578 proteinaceous extracellular matrix
GO:0005615 extracellular space
GO:0005796 Golgi lumen
GO:0031012 extracellular matrix
GO:0043202 lysosomal lumen
Protein Structure and Domains
PDB ID
InterPro IPR000372 Leucine-rich repeat-containing N-terminal
IPR001611 Leucine-rich repeat
IPR003591 Leucine-rich repeat, typical subtype
PFAM PF01462
PF00560
PF13504
PF13855
PRINTS
PIRSF
SMART SM00013
SM00369
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P07585
PhosphoSite PhosphoSite-P07585
TrEMBL F8VNV6
UniProt Splice Variant
Entrez Gene 1634
UniGene Hs.706674
RefSeq
HUGO HGNC:2705
OMIM 125255
CCDS CCDS9041
HPRD 00501
IMGT
EMBL AC007115 AF138300 AF138301 AF138302 AF138303 AF138304 AF491944 AH005442 BC005322 BT019800 CH471054 L01125 L01126 L01127 L01129 L01130 L01131 M14219
GenPept AAA52301 AAB00774 AAB60901 AAD44713 AAD44714 AAD44715 AAF61437 AAF61438 AAH05322 AAL92176 AAV38603 EAW97456 EAW97460