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

FCN2 Gene

protein-coding   GIFtS: 61
GCID: GC09P137772

ficolin (collagen/fibrinogen domain containing lectin) 2...

(Previous name: ficolin (collagen/fibrinogen domain-containing lectin)...)
 Explore 16 diseases affiliated with
FCN2 via our new
 Human Malady Compendium 
Biological research products
for FCN2
    

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

Aliases
Ficolin (Collagen/Fibrinogen Domain Containing Lectin) 2 (Hucolin)1 2     L-Ficolin1
EBP-371 2 3     Ficolin (Collagen/Fibrinogen Domain-Containing Lectin) 2 (Hucolin)1
FCNL1 2 3     Ficolin B2
P351 2     Ficolin-B3
Ficolin-21     Ficolin-Beta1
Collagen/Fibrinogen Domain-Containing Protein 22 3     Ficolin-B3
Serum Lectin P352 3     Ficolin-Beta1
37 KDa Elastin-Binding Protein2 3     Hucolin3

External Ids:    HGNC: 36241   Entrez Gene: 22202   Ensembl: ENSG000001603397   OMIM: 6016245   UniProtKB: Q154853   

Export aliases for FCN2 gene to outside databases

Previous GC identifers: GC09P128922 GC09P129541 GC09P131295 GC09P133211 GC09P134998 GC09P136912 GC09P107236


(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 FCN2:
The product of this gene belongs to the ficolin family of proteins. This family is characterized by the presence of a
leader peptide, a short N-terminal segment, followed by a collagen-like region, and a C-terminal fibrinogen-like
domain. This gene is predominantly expressed in the liver, and has been shown to have carbohydrate binding and opsonic
activities. Alternatively spliced transcript variants encoding different isoforms have been identified. (provided by
RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: FCN2_HUMAN, Q15485
Function: May function in innate immunity through activation of the lectin complement pathway. Calcium-dependent and
GlcNAc-binding lectin. Enhances phagocytosis of S.typhimurium by neutrophils, suggesting an opsonic effect via the
collagen region

Gene Wiki entry for FCN2


(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_000009.11  NC_018920.1  NT_019501.13  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FCN2 gene promoter:
         AREB6   USF1   p53   USF-1   YY1   En-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFCN2 promoter sequence
   Search SABiosciences Chromatin IP Primers for FCN2

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat FCN2


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

Entrez Gene cytogenetic band: 9q34.3   Ensembl cytogenetic band:  9q34.3   HGNC cytogenetic band: 9q34

FCN2 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FCN2 gene location

GeneLoc information about chromosome 9         GeneLoc Exon Structure

GeneLoc location for GC09P137772:  view genomic region     (about GC identifiers)

Start:
137,772,654 bp from pter      End:
137,779,924 bp from pter
Size:
7,271 bases      Orientation:
plus 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: FCN2_HUMAN, Q15485 (See protein sequence)
Recommended Name: Ficolin-2 precursor  
Size: 313 amino acids; 34001 Da
Subunit: Homopolymer; disulfide-linked. Interacts with elastin. Interacts with MASP1 and MASP2
Subcellular location: Secreted
6/10 PDB 3D structures from and Proteopedia for FCN2 (see all 10):
2J0G (3D)        2J0H (3D)        2J0Y (3D)        2J1G (3D)        2J2P (3D)        2J3F (3D)    
Secondary accessions: A6NFG7 A8K478 Q6IS69 Q7M4P4 Q9UC57
Alternative splicing: 2 isoforms:  Q15485-1   Q15485-2   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for FCN2: NX_Q15485

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q15485

  • FCN2 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (2 alternative transcripts): 
    NP_004099.2  NP_056652.1  

    ENSEMBL proteins: 
     ENSP00000291744   ENSP00000291741  

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    Novus Biologicals FCN2 Lysates
    Browse Sino Biological Recombinant Proteins
    Browse ProSpec Recombinant Proteins
    Uscn Proteins for FCN2

    Gene Ontology (GO): 2 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005581collagen IEA--
    GO:0005615extracellular space IEA--


    FCN2 for ontologies           About GeneDecksing



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

    FCN2 for domains           About GeneDecksing

    5 InterPro domains/families:
     IPR014715 Fibrinogen_a/b/g_C_2
     IPR014716 Fibrinogen_a/b/g_C_1
     IPR020837 Fibrinogen_CS
     IPR002181 Fibrinogen_a/b/g_C_dom
     IPR008160 Collagen

    Graphical View of Domain Structure for InterPro Entry Q15485

    ProtoNet protein and cluster: Q15485

    2 Blocks protein families:
    IPB002181 Fibrinogen
    IPB008160 Collagen triple helix repeat


    UniProtKB/Swiss-Prot: FCN2_HUMAN, Q15485
    Domain: The fibrinogen-like domain (FBG) contains potential calcium-binding sites that may be involved in carbohydrate
    binding
    Similarity: Belongs to the ficolin lectin family
    Similarity: Contains 1 collagen-like domain
    Similarity: Contains 1 fibrinogen C-terminal domain


    (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: FCN2_HUMAN, Q15485
    Function: May function in innate immunity through activation of the lectin complement pathway. Calcium-dependent and
    GlcNAc-binding lectin. Enhances phagocytosis of S.typhimurium by neutrophils, suggesting an opsonic effect via the
    collagen region

         Genatlas biochemistry entry for FCN2:
    ficolin 2 (ficolin/opronin p35) lectin family,TGFB1 binding protein P35,expressed in liver

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    Gene Ontology (GO): 5 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003823antigen binding TAS8576206
    GO:0005102receptor binding IEA--
    GO:0005509calcium ion binding TAS8576206
    GO:0030246carbohydrate binding TAS8576206
    GO:0048306calcium-dependent protein binding IPI12421953


    FCN2 for ontologies           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  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Immune response_Alternative complement pathway
    Immune response_Lectin induced complement pathway0.56
    Immune response Lectin Induced complement pathway0.56

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    1 EMD Millipore Pathway for FCN2
        Immune response Lectin Induced complement pathway


    1 GeneGo (Thomson Reuters) Pathway for FCN2
        Immune response Lectin induced complement pathway



    FCN2 for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for FCN2

    STRING Interaction Network Preview (showing 4 interactants - click image to see more details)

    5 Interacting proteins for FCN2 (Q154852, 3 ENSP000002917444) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    LRP1Q079542, 3, ENSP000002430774MINT-8040880 MINT-8040690 I2D: score=1 STRING: ENSP00000243077
    CRPP027412, 3, ENSP000002550304MINT-5223188 I2D: score=2 STRING: ENSP00000255030
    MASP1P487403, ENSP000002962804I2D: score=2 STRING: ENSP00000296280
    MASP2O001873, ENSP000003836904I2D: score=2 STRING: ENSP00000383690
    PTX3P260223I2D: score=1 
    About this table

    Gene Ontology (GO): 3 biological process terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001867complement activation, lectin pathway IEA--
    GO:0007165signal transduction IEA--
    GO:0008228opsonization TAS8576206


    FCN2 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

    FCN2 for compounds           About GeneDecksing

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

    Browse Tocris compounds for FCN2

    1 HMDB Compound for FCN2    About this table
    CompoundSynonyms CAS #PubMed Ids
    CalciumCa (see all 2)7440-70-2--
    7 Novoseek chemical compound relationships for FCN2 gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    serine 62.3 10 19699205 (1), 16305643 (1), 16644773 (1), 19334557 (1) (see all 9)
    mannan 59.7 4 10232391 (2), 19234189 (1)
    n-acetylglucosamine 51.6 4 15879437 (1), 20032467 (1), 15611266 (1)
    1,3-beta-d-glucan 49.9 1 15078867 (1)
    polysaccharide 39.7 6 17680820 (1), 20032467 (1), 18486240 (1)
    sialic acid 29.5 6 20032467 (2), 17938215 (2)
    fibrinogen 12.4 1 20032467 (1)

    Search CenterWatch for drugs/clinical trials and news about FCN2 

    (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 FCN2 gene (4 alternative transcripts): 
    NM_004108.2  NM_015837.2  NM_015838.1  NM_015839.1  

    Unigene Cluster for FCN2:

    Ficolin (collagen/fibrinogen domain containing lectin) 2 (hucolin)
    Hs.54517  [show with all ESTs]
    Unigene Representative Sequence: AK096112
    2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000291744(uc004cfg.1) ENST00000350339(uc004cfh.1)

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    Additional cDNA sequence: 

    AK096112.1 AK290843.1 AK308476.1 BC069572.1 BC069825.1 BC113935.1 D49353.1 

    3 DOTS entries:

    DT.100655023  DT.40257785  DT.91752978 

    18 AceView cDNA sequences:

    BC069825 BC069572 BX098225 AK096112 BX489605 AI052239 NM_015837 BX494192 
    NM_004108 D49353 BX104860 AI078046 NM_015838 NM_015839 H62841 H62842 
    H62781 AI056206 

    GeneLoc Exon Structure


    (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

    FCN2 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TCGTGATTCT

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

    About this image
    See FCN2 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FCN2

    SOURCE GeneReport for Unigene cluster: Hs.54517

    UniProtKB/Swiss-Prot: FCN2_HUMAN, Q15485
    Tissue specificity: Expressed by the liver and secreted in plasma

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    In Situ
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    (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 animals.

    Orthologs for FCN2 gene from 3/12 species (see all 12)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves FCN21 ficolin (collagen/fibrinogen domain containing lectin) more 66.54(n)
    64.09(a)
      417298  XM_415571.3  XP_415571.2 
    African clawed frog
    (Xenopus laevis)
    Amphibia AB091342.12   -- 75.54(n)    AB091342.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG302803   -- 44(a)
    (best of 8)
        --


    ENSEMBL Gene Tree for FCN2 (if available)
    TreeFam Gene Tree for FCN2 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FCN2 gene
    TNR2  FIBCD12  FCN32  FCN12  TNXB2  TNN2  MFAP42  FN12  
    TNC2  ANGPTL52  
    18/40 SIMAP similar genes for FCN2 using alignment to 2 protein entries:     FCN2_HUMAN (see all proteins) (see all similar genes):
    FCN1    DKFZp781B1032    ANGPTL7    FCN3    FIBCD1    TNN
    TNR    TNC    TNC variant protein    ANGPT1    ANGPT4    ANGPTL2
    COL9A1    TNXB    MFAP4    FGL1    LFIRE1    ANGPTL4

    FCN2 for paralogs           About GeneDecksing


    1 Pseudogenes.org Pseudogene for FCN2
    PGOHUM00000236787


    (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

    10/279 NCBI SNPs in FCN2 are shown (see all 279    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 9 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs747064121,2
    F,--107234315(+) AAACAT/CTGTTA 2 -- us2k11Minor allele frequency- C:0.13WA 118
    rs775703391,2
    F,--107234884(+) TCCATG/AGAGCC 2 -- us2k11Minor allele frequency- A:0.03NA 120
    rs558486541,2
    C,F,--107234888(+) TGGAGC/ACTGTG 2 -- us2k11Minor allele frequency- A:0.08WA 118
    rs38111431,2
    C,F,H,--107235235(-) GTGGGG/TCCCCA 2 -- us2k19Minor allele frequency- T:0.09NS EA 1188
    rs38111411,2
    C,H--107235567(-) CTGTTT/GCCTGG 2 -- us2k12Minor allele frequency- G:0.01NS NA 122
    rs746930031,2
    C,--107235719(+) CCCATA/GACCAG 2 -- us2k10--------
    rs558091101,2
    C,F,--107235886(+) CCAAGG/ACCACA 2 -- us2k11Minor allele frequency- A:0.08WA 118
    rs123440511,2
    C,F,H,--107235923(+) AGACCG/ATCCCC 2 -- us2k16Minor allele frequency- A:0.02NS EA CSA WA 532
    rs38111391,2
    C,F,H,--107235966(-) CCCCCG/ACCCCT 2 -- us2k14Minor allele frequency- A:0.04EA NS 418
    rs725511211,2
    C,--107236068(+) TTGGAG/ATCTGA 2 -- us2k11Minor allele frequency- A:0.01NA 120

    HapMap Linkage Disequilibrium report for FCN2 (137772654 - 137779924 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for FCN2: --
    Human Gene Mutation Database (HGMD): FCN2

    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing FCN2
    DNA2.0 Custom Variant and Variant Library Synthesis for FCN2

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

    FCN2 for disorders           About GeneDecksing

    OMIM gene information: 601624    OMIM disorders: --

    16 diseases for FCN2:    About MalaCards
    rheumatic fever    bronchiectasis    cystic fibrosis    behcet's disease
    pemphigus    rheumatoid arthritis    leprosy    hepatitis b
    gout    sarcoidosis    fibrosis    arthritis
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    Human Genome Epidemiology (HuGE) Navigator: FCN2 (13 documents)

    Export disorders for FCN2 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)
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    PubMed articles for FCN2 gene, integrated from 9 sources (see all 101):
    (articles sorted by number of sources associating them with FCN2)
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    1. Cloning and characterization of the human lectin P35 gene and its related gene. (PubMed id 8884275)1, 2, 3, 9 Endo Y.... Fujita T. (1996)
    2. A novel human serum lectin with collagen- and fibrinogen-like domains that functions as an opsonin. (PubMed id 8576206)1, 2, 9 Matsushita M.... Mizuochi T. (1996)
    3. Hucolin, a new corticosteroid-binding protein from human plasma with structural similarities to ficolins, transforming growth factor-beta 1-binding proteins. (PubMed id 7498469)1, 2, 9 Edgar P.F. (1995)
    4. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    5. Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 gene. (PubMed id 17680820)1, 9 Cedzynski M....Kilpatrick D.C. (2007)
    6. Ficolin 2 (FCN2) functional polymorphisms and the ris k of rheumatic fever and rheumatic heart disease. (PubMed id 19664148)1, 9 Messias-Reason I.J....Kun J.F. (2009)
    7. Two factors of the lectin pathway of complement, l-ficolin and mannan-binding lectin, and their associations with prematurity, low birthweight and infections in a large cohort of Polish neonates. (PubMed id 18950864)1, 9 St Swierzko A....Kilpatrick D.C. (2008)
    8. The impact of FCN2 polymorphisms and haplotypes on the Ficolin-2 serum levels. (PubMed id 17386030)1, 9 Munthe-Fog L....Garred P. (2007)
    9. Synergy between ficolin-2 and pentraxin 3 boosts inna te immune recognition and complement deposition. (PubMed id 19632990)1, 9 Ma Y.J....Garred P. (2009)
    10. Functional polymorphisms in the FCN2 gene are not associated with invasive pneumococcal disease. (PubMed id 17382393)1, 9 Chapman S.J....Hill A.V. (2007)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
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    Entrez Gene: 2220 HGNC: 3624 AceView: FCN2 Ensembl:ENSG00000160339 euGenes: HUgn2220
    ECgene: FCN2 H-InvDB: FCN2

    (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 FCN2 Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for FCN2 gene:
    Search GeneIP for patents involving FCN2

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



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