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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

DCN Gene

protein-coding   GIFtS: 69
GCID: GC12M091472

decorin

 Explore 116 diseases affiliated with
DCN via our new
 Human Malady Compendium 
Biological research products
for DCN
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Decorin1     PGII2
SLRR1B1 2 3     PGS22
DSPG21 2     Decorin Proteoglycan2
Bone Proteoglycan II2 3     Dermatan Sulphate Proteoglycans II2
PG-S22 3     Proteoglycan Core Protein2
PG402 3     Small Leucine-Rich Protein 1B2
CSCD2 5     

External Ids:    HGNC: 27051   Entrez Gene: 16342   Ensembl: ENSG000000114657   OMIM: 1252555   UniProtKB: P075853   

Export aliases for DCN gene to outside databases

Previous GC identifers: GC12M090861 GC12M091986 GC12M090041 GC12M088606


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for DCN:
The protein encoded by this gene is a small cellular or pericellular matrix proteoglycan that is closely related in
structure to biglycan protein. The encoded protein and biglycan are thought to be the result of a gene duplication.
This protein is a component of connective tissue, binds to type I collagen fibrils, and plays a role in matrix
assembly. It contains one attached glycosaminoglycan chain. This protein is capable of suppressing the growth of
various tumor cell lines. There are multiple alternatively spliced transcript variants known for this gene. This gene
is a candidate gene for Marfan syndrome. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: PGS2_HUMAN, P07585
Function: May affect the rate of fibrils formation

Gene Wiki entry for DCN (Decorin)


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000012.11  NC_018923.1  NT_029419.12  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the DCN gene promoter:
         AP-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): DCN promoter sequence
   Search SABiosciences Chromatin IP Primers for DCN

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat DCN


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 12q21.33   Ensembl cytogenetic band:  12q21.33   HGNC cytogenetic band: 12q23

DCN Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
DCN gene location

GeneLoc information about chromosome 12         GeneLoc Exon Structure

GeneLoc location for GC12M091472:  view genomic region     (about GC identifiers)

Start:
91,539,025 bp from pter      End:
91,576,900 bp from pter
Size:
37,876 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: PGS2_HUMAN, P07585 (See protein sequence)
Recommended Name: Decorin precursor  
Size: 359 amino acids; 39747 Da
Subunit: Binds to type I and type II collagen, fibronectin and TGF-beta. Forms a ternary complex with MFAP2 and ELN.
Interacts with DPT (By similarity)
Subcellular location: Secreted, extracellular space, extracellular matrix
Secondary accessions: Q9P0Z0 Q9P0Z1 Q9Y5N8 Q9Y5N9
Alternative splicing: 5 isoforms:  P07585-1   P07585-2   P07585-3   P07585-4   P07585-5   

Explore the universe of human proteins at neXtProt for DCN: NX_P07585

Post-translational modifications:

  • The attached glycosaminoglycan chain can be either chondroitin sulfate or dermatan sulfate depending upon the tissue of
  • origin1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P07585

  • DCN Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (6 alternative transcripts): 
    NP_001911.1  NP_598010.1  NP_598011.1  NP_598012.1  NP_598013.1  NP_598014.1  

    ENSEMBL proteins: 
     ENSP00000052754   ENSP00000448853   ENSP00000447654   ENSP00000413723   ENSP00000399815  
     ENSP00000447674   ENSP00000446530   ENSP00000398514   ENSP00000449408   ENSP00000449782  
     ENSP00000447886   ENSP00000449014   ENSP00000449438   ENSP00000446527   ENSP00000448857  
     ENSP00000448057   ENSP00000448274   ENSP00000228329   ENSP00000302031   ENSP00000376862  
     ENSP00000401021  
    Reactome Protein details: P07585
    Human Recombinant Protein Products: 
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    Novus Biologicals DCN Lysates
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    Uscn Proteins for DCN

    Gene Ontology (GO): 5/7 cellular component terms (GO ID links to tree view) (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005576extracellular region TAS--
    GO:0005578proteinaceous extracellular matrix ----
    GO:0005589collagen type VI IEA--
    GO:0005615extracellular space IDA--
    GO:0005796Golgi lumen TAS--


    DCN for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for DCN


    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    DCN for domains           About GeneDecksing

    4 InterPro domains/families:
     IPR001611 Leu-rich_rpt
     IPR003591 Leu-rich_rpt_typical-subtyp
     IPR000372 LRR-contain_N
     IPR016352 SLRP_I_decor/aspor/byglycan

    Graphical View of Domain Structure for InterPro Entry P07585

    ProtoNet protein and cluster: P07585

    2 Blocks protein families:
    IPB000372 Cysteine-rich flanking region
    IPB001611 Leucine-rich repeat signature


    UniProtKB/Swiss-Prot: PGS2_HUMAN, P07585
    Similarity: Belongs to the small leucine-rich proteoglycan (SLRP) family. SLRP class I subfamily
    Similarity: Contains 12 LRR (leucine-rich) repeats


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: PGS2_HUMAN, P07585
    Function: May affect the rate of fibrils formation

         Genatlas biochemistry entry for DCN:
    decorin,small collagen-binding proteoglycan of the extracellular matrix,leucine-rich repeats (LRR) family,involved in
    the differentiation of retinal glanglion cells

    miRNA
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    2 QIAGEN miScript miRNA Assays for microRNAs that regulate DCN:
    hsa-miR-374c hsa-miR-655
    SwitchGear 3'UTR luciferase reporter plasmidDCN 3' UTR sequence
    Inhib. RNA
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    Clone
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for DCN

    Gene Ontology (GO): 4 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005518collagen binding IEA--
    GO:0005539glycosaminoglycan binding IEA--
    GO:0047485protein N-terminus binding IEA--
    GO:0050840extracellular matrix binding IEA--


    DCN for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for DCN:
     Increased gamma-H2AX phosphory 

    Animal Models:
         Mouse knock-out Dcntm1Ioz for DCN
         15/18 MGI mutant phenotypes (inferred from 1 allele(MGI details for Dcn) (see all 18):
     behavior/neurological  cellular  craniofacial  digestive/alimentary  endocrine/exocrine gland 
     growth/size  hematopoietic system  homeostasis/metabolism  immune system  integument 
     mortality/aging  muscle  renal/urinary system  reproductive system  respiratory system 

    DCN for phenotypes           About GeneDecksing


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section

    Unified GeneCards pathways - 5/9 super-pathways (see all 9About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1MPS IIIC - Sanfilippo syndrome C
    8/15 pathways (see all 15)
    MPS IIIC - Sanfilippo syndrome C1.00
    MPS IIID - Sanfilippo syndrome D1.00
    MPS I - Hurler syndrome1.00
    MPS IX - Natowicz syndrome1.00
    Mucopolysaccharidoses1.00
    MPS II - Hunter syndrome1.00
    MPS IV - Morquio syndrome A1.00
    Glycosaminoglycan metabolism1.00
    2DSPGs are secreted
    DSPG and CSPG translocate to the lysosome for degradation1.00
    CSPG is secreted1.00
    DSPGs are secreted1.00
    Dermatan sulfate biosynthesis0.70
    CS is cleaved from its proteoglycan1.00
    CS/DS degradation0.54
    DS is cleaved from its proteoglycan1.00
    3A tetrasaccharide linker sequence is required for GAG synthesis
    A tetrasaccharide linker sequence is required for GAG synthesis1.00
    Chondroitin sulfate/dermatan sulfate metabolism0.54
    4Disease
    Disease1.00
    5Metabolism
    Metabolism1.00

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    1 R&D Systems Pathway for DCN
        Articular Cartilage Extracellular Matrix


    1 BioSystems Pathway for DCN 
        Validated transcriptional targets of AP1 family members Fra1 and Fra2

    5/27        Reactome Pathways for DCN (see all 27)
        Chondroitin sulfate/dermatan sulfate metabolism
    MPS VI - Maroteaux-Lamy syndrome
    Metabolism
    DSPG and CSPG translocate to the lysosome for degradation
    Disease


    1         Kegg Pathway  (Kegg details for DCN):
        TGF-beta signaling pathway


    DCN for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for DCN

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/70 Interacting proteins for DCN (P075853 ENSP000000527544) via UniProtKB, MINT, STRING, and/or I2D (see all 70)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    COL14A1Q057073, ENSP000002978484I2D: score=2 STRING: ENSP00000297848
    PLA2G2AP145553, ENSP000003642524I2D: score=2 STRING: ENSP00000364252
    COL1A1P024523, ENSP000002259644I2D: score=1 STRING: ENSP00000225964
    COL4A4P534203, ENSP000003798664I2D: score=1 STRING: ENSP00000379866
    COL4A6Q140313, ENSP000003612904I2D: score=1 STRING: ENSP00000361290
    About this table

    Gene Ontology (GO): 5/16 biological process terms (GO ID links to tree view) (see all 16):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001822kidney development IEA--
    GO:0001890placenta development IEA--
    GO:0005975carbohydrate metabolic process TAS--
    GO:0007519skeletal muscle tissue development IEA--
    GO:0007568aging IEA--


    DCN for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    DCN for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for DCN

    1 DrugBank Compound for DCN    About this table
    CompoundSynonyms CAS #TypeActionsPubMed Ids
    Tris(Hydroxymethyl)Aminomethane-- --target--17139284 17016423 10592235

    10/70 Novoseek chemical compound relationships for DCN gene (see all 70)    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    glycosaminoglycan 90.2 116 9726998 (5), 12372409 (4), 2108171 (3), 17651433 (3) (see all 73)
    dermatan sulfate 89.5 90 10536375 (4), 12531251 (2), 10749870 (2), 9727420 (2) (see all 61)
    chondroitin 89.3 60 1605630 (3), 1711290 (2), 19557760 (2), 1744124 (2) (see all 46)
    chondroitin sulfate 86.1 76 17286067 (6), 12531251 (3), 16498599 (3), 10536375 (3) (see all 50)
    dermatan 83.7 17 9168858 (2), 10749870 (1), 7741696 (1), 9148753 (1) (see all 12)
    keratan sulfate 82.8 11 8546427 (2), 20139802 (2), 1376375 (1), 8760363 (1) (see all 8)
    galactosaminoglycan 80.3 7 12495820 (1), 19444760 (1), 8635597 (1), 12668676 (1) (see all 5)
    dspg 79.3 11 8457255 (2), 16902402 (2), 1599405 (1), 10648661 (1) (see all 7)
    l-iduronate 78.8 1 12207034 (1)
    heparan sulfate 70.3 20 10585870 (2), 1639087 (1), 8397099 (1), 9328841 (1) (see all 16)

    Search CenterWatch for drugs/clinical trials and news about DCN / PGS2 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for DCN gene (6 alternative transcripts): 
    NM_001920.3  NM_133503.2  NM_133504.2  NM_133505.2  NM_133506.2  NM_133507.2  

    Unigene Cluster for DCN:

    Decorin
    Hs.156316  [show with all ESTs]
    Unigene Representative Sequence: NM_001920
    18/22 Ensembl transcripts including schematic representations, and UCSC links where relevant (see all 22):
    ENST00000052754(uc001tbo.3 uc001tbp.3 uc001tbq.3 uc001tbr.3 uc001tbu.3)
    ENST00000548218 ENST00000552962 ENST00000420120 ENST00000441303 ENST00000547568
    ENST00000546391 ENST00000456569 ENST00000550758 ENST00000547937 ENST00000552145
    ENST00000550563 ENST00000549513 ENST00000546370 ENST00000546745 ENST00000550099
    ENST00000551354 ENST00000548768

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    Inhib. RNA
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    Additional cDNA sequence: 

    AF138300.1 AF138301.1 AF138302.1 AF138303.1 AF138304.1 AK291309.1 AL355731.1 BC005322.1 
    BT019800.1 BX571756.1 CR407676.1 CR541946.1 

    24/65 DOTS entries (see all 65):

    DT.92468924  DT.99954679  DT.100891103  DT.100042199  DT.95305589  DT.100806878  DT.100032839  DT.100891123 
    DT.100723534  DT.92468934  DT.100733720  DT.100042195  DT.100891111  DT.100042205  DT.95305581  DT.100891114 
    DT.92468931  DT.95305642  DT.121111226  DT.405392  DT.100891081  DT.92468868  DT.100891126  DT.100042193 

    24/2381 AceView cDNA sequences (see all 2381):

    BQ045071 BQ180873 CA413215 BX343891 CA334866 AA374374 AA359178 BU727376 
    CA441756 CD518494 AU119827 BU146592 CD514958 CA412742 BM874008 BM994885 
    BQ772943 BQ009059 CA440729 BF941175 AW028006 CN480192 BQ007604 BM989449 

    GeneLoc Exon Structure

    5/17 Alternative Splicing Database (ASD) splice patterns (SP) for DCN (see all 17)    About this scheme

    ExUns: 1a · 1b · 1c · 1d ^ 2 ^ 3 ^ 4 ^ 5a · 5b · 5c · 5d · 5e · 5f ^ 6 ^ 7 ^ 8a · 8b · 8c ^ 9 ^ 10a · 10b ^ 11a · 11b ^ 12a · 12b · 12c ·
    SP1:                          -     -     -     -     -     -     -     -     -     -                             -     -     -                                 
    SP2:                                                                                -                             -     -     -                                 
    SP3:                                                                                                              -     -     -                                 
    SP4:                                                                                                              -     -     -     -     -                     
    SP5:                          -     -     -     -     -     -     -     -     -     -                             -     -     -     -     -     -     -     -   

    ExUns: 12d · 12e ^ 13a · 13b ^ 14 ^ 15a · 15b · 15c · 15d ^ 16a · 16b · 16c · 16d · 16e
    SP1:                                                                                    
    SP2:                                                                                    
    SP3:                                                                                    
    SP4:                                                                                    
    SP5:  -     -     -     -                                                               


    ECgene alternative splicing isoforms for DCN

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    DCN expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: ACTTATTATG

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image

    DCN expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    10/15 LifeMap In Vivo Development Anatomical Compartments/Cells (see all 15
    Tissue Anatomical Compartment CellCategory (developmental path)
    BoneCaudal Endochondral BonesEndochondral OsteoblastsBone
    BoneEndochondral Facial BonesEndochondral OsteoblastsBone
    BoneRostral Endochondral Facial BonesEndochondral OsteoblastsBone
    CartilageCervical Intervertebral DiscIntervertebral Disc Nucleus Pulposus CellsCartilage
    CartilageLumbar Intervertebral DiscIntervertebral Disc Nucleus Pulposus CellsCartilage
    CartilageSacral Intervertebral DiscIntervertebral Disc Nucleus Pulposus CellsCartilage
    CartilageThoracic Intervertebral DiscIntervertebral Disc Nucleus Pulposus CellsCartilage
    Tendons & LigamentsAxial Tendon PrimordiaEarly Tenocyte CellsTendons & Ligaments
    Tendons & LigamentsAxial Tendons and LigamnetsTenocytesTendons & Ligaments
    Tendons & LigamentsLimb Tendon PrimordiaEarly Tenocyte CellsTendons & Ligaments
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 10/18 LifeMap Cells (see all 18
    NameCategory
    PureStem™ mesenchymal Progenitor SK11 (Embryonic Progenitor Cell)Adipose, Bone, Cartilage
    PureStem™ myogenic progenitor Z11 (Embryonic Progenitor Cell)Heart, Myocardium, Smooth Muscle
    PureStem™ mesenchymal progenitor 7PEND24 (Embryonic Progenitor Cell)Cartilage, Neural Crest
    PureStem™ progenitor EN13 (Embryonic Progenitor Cell)
    PureStem™ progenitor EN7 (Embryonic Progenitor Cell)
    PureStem™ progenitor RASMO12 (Embryonic Progenitor Cell)
    PureStem™ progenitor W8 (Embryonic Progenitor Cell)
    Connective tissue progenitor cells (Generation of connec...)
    Syncytiotrophoblast-like cells (Generation of syncyt...)
    Trophoblast-like cells (Generation of tropho...)

    See DCN Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for DCN

    SOURCE GeneReport for Unigene cluster: Hs.156316
        SABiosciences Expression via Pathway-Focused PCR Arrays including DCN: 
              Fibrosis in human mouse rat
              Cell Lineage Identification in human mouse rat
              TGFB/BMP Signaling Pathway in human mouse rat

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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for DCN

    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of chordates.

    Orthologs for DCN gene from 4/14 species (see all 14)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves DCN1 decorin 75.35(n)
    78.15(a)
      417892  NM_001030747.1  NP_001025918.1 
    lizard
    (Anolis carolinensis)
    Reptilia DCN6
    --
    78(a)
    1 ↔ 1
    5(32298151-32330686)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.245052 Xenopus laevis transcribed sequence with moderate similarity more 73.75(n)    CB564863.1 
    zebrafish
    (Danio rerio)
    Actinopterygii BC044206.12   -- 75.07(n)   64698  BC044206.1 


    ENSEMBL Gene Tree for DCN (if available)
    TreeFam Gene Tree for DCN (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for DCN gene
    OGN2  OPTC2  PODN2  PODNL12  FMOD2  PRELP2  KERA2  ASPN2  
    OMD2  BGN2  EPYC2  ECM22  LUM2  
    18/23 SIMAP similar genes for DCN using alignment to 12 protein entries:     PGS2_HUMAN (see all proteins) (see all similar genes):
    LRIG1    SLIT2    BGN    LGR5    ASPN    SLIT1
    PXDNL    LRRC3B    LGR6    AMIGO1    LRRC70    PXDN
    ZSCAN2    AMIGO3    SLIT3    PODN    LGR4    TRIL

    DCN for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/699 NCBI SNPs in DCN are shown (see all 699    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 12 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs31382911,2
    C,F,H,--88606763(-) TAGATG/ATATTA 6 -- ds500113Minor allele frequency- A:0.12NS EA NA WA 1324
    rs353798121,2
    F,--88607227(+) TCTCAA/GATGAG 6 -- ut311Minor allele frequency- G:0.03NA 120
    rs31382901,2
    C,F,H,--88607284(-) AATTTC/TCAGGA 6 -- ut31 ese37Minor allele frequency- T:0.02NS EA 556
    rs31382891,2
    C,F,H--88607414(-) GCCATT/CTTCAG 6 -- ut317Minor allele frequency- C:0.01NS EA NA 426
    rs18033431,2
    C,F,A,H,--88607553(-) ATGTCA/GTTGCT 6 -- ut31 ese314Minor allele frequency- G:0.02NS EA NA 1626
    rs18033421,2
    C--88607788(-) CTACCT/CTCATA 12 /P /L mis1 syn12Minor allele frequency- C:0.00NA 4
    rs31382881,2
    C,F,A,H,--88607872(-) AAAAAA/G/TAATAA 6 -- int111NS NA WA 1084
    rs584550411,2
    --88607953(+) TGGAGG/TGCAGT 6 -- int10--------
    rs31382871,2
    C,F,H,--88608199(-) AAAGTG/TGGGCC 6 -- int113Minor allele frequency- T:0.03NS EA NA WA 1418
    rs31382861,2
    C,F,H,--88608705(-) agagtA/Ggaagg 6 -- int18Minor allele frequency- G:0.06NS EA WA 632

    HapMap Linkage Disequilibrium report for DCN (91539025 - 91576900 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 2 variations for DCN
         2 CNVs: 53592 4785
    Human Gene Mutation Database (HGMD): DCN

    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing DCN
    DNA2.0 Custom Variant and Variant Library Synthesis for DCN

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    DCN for disorders           About GeneDecksing

    OMIM gene information: 125255   
    OMIM disorders: 610048  
    UniProtKB/Swiss-Prot: PGS2_HUMAN, P07585
  • Defects in DCN are the cause of congenital stromal corneal dystrophy (CSCD) [MIM:610048]. Corneal dystrophies
  • are inherited, bilateral, primary alterations of the cornea that are not associated with prior inflammation or
    secondary to systemic disease. Most show autosomal dominant inheritance

    20/116 diseases for DCN (see all 116):    About MalaCards
    marfan syndrome    ehlers-danlos syndrome    spinal cord injury    osteogenesis imperfecta
    bullous keratopathy    congenital stromal corneal dystrophy    dupuytren contracture    epiphyseal dysplasia
    corneal dystrophy    aortic aneurysm    muscular dystrophy    gingival overgrowth
    crouzon syndrome    odontogenic myxoma    multiple epiphyseal dysplasia    pre-eclampsia
    abdominal aortic aneurysm    duchenne muscular dystrophy    localized scleroderma    lichen sclerosus

    3 diseases from the University of Copenhagen DISEASES database for DCN:
    Lyme disease     Ehlers-Danlos syndrome     Osteoarthritis

    10/89 Novoseek disease relationships for DCN gene (see all 89)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    collagen fibril 82.8 67 18622092 (4), 17530890 (3), 2059554 (3), 17651433 (3) (see all 50)
    scars hypertrophic 61.1 23 9682679 (5), 19167828 (4), 17374457 (3), 10692030 (2) (see all 8)
    osteoarthritis 42.2 4 11406617 (1), 18620607 (1), 8456642 (1), 11597178 (1)
    scar 41.2 28 15312466 (5), 10692030 (3), 7544762 (2), 11039776 (2) (see all 13)
    ehlers-danlos syndrome 39 4 11532373 (1), 16583246 (1), 15859521 (1), 17651433 (1)
    bullous keratopathy 36.3 1 9727420 (1)
    psach 36 1 11691584 (1)
    osteosarcoma 34 16 18497961 (4), 18661352 (3), 18505923 (2), 2254344 (2) (see all 9)
    crouzon syndrome 33.9 1 10384983 (1)
    keloid 27.9 17 20386290 (6), 19268470 (6), 8949432 (1), 8262136 (1)

    GeneTests: DCN
    Congenital Stromal Corneal Dystrophy

    Genetic Association Database (GAD): DCN
    Human Genome Epidemiology (HuGE) Navigator: DCN (13 documents)

    Export disorders for DCN gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for DCN gene, integrated from 9 sources (see all 792):
    (articles sorted by number of sources associating them with DCN)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. The human decorin gene: intron-exon organization, discovery of two alternatively spliced exons in the 5' untranslated region, and mapping of the gene to chromosome 12q23. (PubMed id 8432526)1, 2, 3, 9 Danielson K.G.... Iozzo R.V. (1993)
    2. Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene. (PubMed id 15671264)1, 2, 9 Bredrup C.... Boman H. (2005)
    3. The Decorin gene 179 allelic variant is associated with a slower progression of renal disease in patients with type 1 diabetes. (PubMed id 12187087)1, 4, 9 De Cosmo S....Viberti G.C. (2002)
    4. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    5. Human decorin gene: intron-exon junctions and chromosomal localization. (PubMed id 8432527)1, 2 Vetter U.... Fisher L.W. (1993)
    6. Dermatan sulphate proteoglycans of human articular cartilage. The properties of dermatan sulphate proteoglycans I and II. (PubMed id 2590169)1, 2 Roughley P.J. and White R.J. (1989)
    7. Purification and partial characterization of small proteoglycans I and II, bone sialoproteins I and II, and osteonectin from the mineral compartment of developing human bone. (PubMed id 3597437)1, 2 Fisher L.W.... Termine J.D. (1987)
    8. Primary structure of an extracellular matrix proteoglycan core protein deduced from cloned cDNA. (PubMed id 3484330)1, 2 Krusius T. and Ruoslahti E. (1986)
    9. Endocytosis of the dermatan sulfate proteoglycan decorin utilizes multiple pathways and is modulated by epidermal growth factor receptor signaling. (PubMed id 17335953)1, 9 Feugaing D.D....Gotte M. (2007)
    10. Purification and characterization of decorin from the culture media of MRC-5 cells. (PubMed id 15147741)1, 9 Honda E. and Munakata H. (2004)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 1634 HGNC: 2705 AceView: DCN Ensembl:ENSG00000011465 euGenes: HUgn1634
    ECgene: DCN Kegg: 1634 H-InvDB: DCN

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for DCN Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for DCN Genetics and Cytogenetics in Oncology and Haematology
    SeattleSNPshttp://pga.gs.washington.edu/data/dcn/

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for DCN gene:
    Search GeneIP for patents involving DCN

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
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    About This Section

     
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