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

FCRL3 Gene

protein-coding   GIFtS: 53
GCID: GC01M157646

Fc receptor-like 3

 Explore 29 diseases affiliated with
FCRL3 via our new
 Human Malady Compendium 
Biological research products
for FCRL3
    

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

Aliases
Fc Receptor-Like 31 2     SH2 Domain-Containing Phosphatase Anchor Protein 22 3
FCRH31 2 3 5     SPAP2a1
IFGP31 2 3     SPAP2b1
IRTA31 2 3     SPAP2c1
SPAP21 2 3     SPAP2d1
CD307c1 2     SPAP2e1
FcR-Like Protein 32 3     Fc Receptor-Like Protein 32
Immune Receptor Translocation-Associated Protein 32 3     Immunoglobulin Superfamily Receptor Translocation Associated Protein 32
Fc Receptor Homolog 32 3     FcRH33
HIFGP31     FcRL33
IFGP Family Protein 32 3     CD307c Antigen3

External Ids:    HGNC: 185061   Entrez Gene: 1153522   Ensembl: ENSG000001608567   OMIM: 6065105   UniProtKB: Q96P313   

Export aliases for FCRL3 gene to outside databases

Previous GC identifers: GC01M154460 GC01M155912 GC01M129005


(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 FCRL3:
This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like
glycoproteins clustered on the long arm of chromosome 1. The encoded protein contains immunoreceptor-tyrosine
activation motifs and immunoreceptor-tyrosine inhibitory motifs in its cytoplasmic domain and may play a role in
regulation of the immune system. Mutations in this gene have been associated with rheumatoid arthritis, autoimmune
thyroid disease, and systemic lupus erythematosus. (provided by RefSeq, Jul 2008)

Gene Wiki entry for FCRL3


(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_000001.10  NC_018912.1  NT_004487.19  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FCRL3 gene promoter:
         AML1a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFCRL3 promoter sequence
   Search SABiosciences Chromatin IP Primers for FCRL3

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat FCRL3


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

Entrez Gene cytogenetic band: 1q21-q22   Ensembl cytogenetic band:  1q23.1   HGNC cytogenetic band: 1q21-q22

FCRL3 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FCRL3 gene location

GeneLoc information about chromosome 1         GeneLoc Exon Structure

GeneLoc location for GC01M157646:  view genomic region     (about GC identifiers)

Start:
157,646,271 bp from pter      End:
157,670,775 bp from pter
Size:
24,505 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: FCRL3_HUMAN, Q96P31 (See protein sequence)
Recommended Name: Fc receptor-like protein 3 precursor  
Size: 734 amino acids; 80856 Da
Subunit: Interacts with PTPN6, PTPN11, SYK and ZAP70
Subcellular location: Cell membrane; Single-pass type I membrane protein
Secondary accessions: A0N0M4 A8MTH7 D3DVD2 Q5VXZ8 Q8N6S2 Q96LA4 Q96P27 Q96P28 Q96P29 Q96P30
Alternative splicing: 7 isoforms:  Q96P31-1   Q96P31-2   Q96P31-3   Q96P31-4   Q96P31-5   Q96P31-6   Q96P31-7   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for FCRL3: NX_Q96P31

Post-translational modifications:

  • Phosphorylated on cytoplasmic tyrosines; required for interaction with protein tyrosine phosphatases and protein
  • tyrosine kinases1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q96P31

  • FCRL3 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_443171.2  
    ENSEMBL proteins: 
     ENSP00000433430   ENSP00000435487   ENSP00000357169   ENSP00000434331   ENSP00000357167  
     ENSP00000292392  

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    Uscn Proteins for FCRL3

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005886plasma membrane IEA--
    GO:0016021integral to membrane IEA--


    FCRL3 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

    FCRL3 for domains           About GeneDecksing

    4 InterPro domains/families:
     IPR003598 Ig_sub2
     IPR013783 Ig-like_fold
     IPR007110 Ig-like_dom
     IPR003599 Ig_sub

    Graphical View of Domain Structure for InterPro Entry Q96P31

    ProtoNet protein and cluster: Q96P31

    2 Blocks protein families:
    IPB002052 N-6 Adenine-specific DNA methylase
    IPB003598 Immunoglobulin C-2 type


    UniProtKB/Swiss-Prot: FCRL3_HUMAN, Q96P31
    Similarity: Contains 6 Ig-like C2-type (immunoglobulin-like) domains


    (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

    miRNA
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    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat FCRL3
    1 QIAGEN miScript miRNA Assays for microRNA that regulate FCRL3:
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    Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0004872receptor activity ----


    FCRL3 for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for FCRL3:
     Synthetic lethal with Ras 

    Animal Models:
         Mouse knock-out Fcrl5tm1Lex for FCRL3
         1 MGI phenotypic allele for Fcrl5 (no phenotypes)

    FCRL3 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



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for FCRL3

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

    4 Interacting proteins for FCRL3 (Q96P313 ENSP000003571674) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    ZAP70P434033, ENSP000002649724I2D: score=2 STRING: ENSP00000264972
    PTPN11Q061243, ENSP000003409444I2D: score=1 STRING: ENSP00000340944
    PTPN6P293503, ENSP000003915924I2D: score=1 STRING: ENSP00000391592
    SYKP434053, ENSP000003648984I2D: score=1 STRING: ENSP00000364898
    About this table

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

    Browse Tocris compounds for FCRL3
    Search CenterWatch for drugs/clinical trials and news about FCRL3 

    (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 FCRL3 gene (2 alternative transcripts): 
    NM_052939.3  NM_001024667.1  

    Unigene Cluster for FCRL3:

    Fc receptor-like 3
    Hs.292449  [show with all ESTs]
    Unigene Representative Sequence: NM_052939
    12 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000477837 ENST00000492769 ENST00000480682 ENST00000494724 ENST00000368186
    ENST00000485028 ENST00000368184(uc001fqx.4 uc001fqy.4 uc001fqz.4 uc009wsn.3 uc009wso.3 uc001frb.3)
    ENST00000292392(uc001frc.1) ENST00000473231(uc001fra.3) ENST00000468507
    ENST00000478179 ENST00000496769

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    Additional cDNA sequence: 

    AF459027.1 AK098122.1 AK125622.1 AK301257.1 AY043466.1 BC013698.1 BC028933.1 

    11 DOTS entries:

    DT.97839192  DT.99936266  DT.99956633  DT.92325152  DT.100017548  DT.95156352  DT.97839193  DT.97839190 
    DT.95090097  DT.95156353  DT.97839195 

    24/55 AceView cDNA sequences (see all 55):

    AI357107 AA485839 AA485705 BC028933 NM_052939 AK098122 AL833391 AA765694 
    BM455913 AA972108 AW403530 BM458374 AW576446 BM458414 AF459027 BF514552 
    BF343316 BG105889 BI836314 BM459359 AF416903 AY043466 AW504347 AK125622 

    GeneLoc Exon Structure

    5/8 Alternative Splicing Database (ASD) splice patterns (SP) for FCRL3 (see all 8)    About this scheme

    ExUns: 1 ^ 2 ^ 3 ^ 4 ^ 5a · 5b · 5c ^ 6 ^ 7a · 7b ^ 8a · 8b ^ 9 ^ 10 ^ 11 ^ 12 ^ 13
    SP1:                                                                                                      
    SP2:                                      -                                                               
    SP3:                                            -     -     -                                             
    SP4:                                                                                                      
    SP5:        -                                                                                             


    ECgene alternative splicing isoforms for FCRL3

    (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

    FCRL3 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: CAGTGCTCTA

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

    About this image
    See FCRL3 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FCRL3

    SOURCE GeneReport for Unigene cluster: Hs.292449

    UniProtKB/Swiss-Prot: FCRL3_HUMAN, Q96P31
    Tissue specificity: Primarily expressed in secondary lymphoid tissues by mature subsets of B-cells. Detected in spleen,
    lymph node, peripheral blood lymphocytes, thymus, bone marrow, kidney, salivary gland, adrenal gland and uterus.
    Expressed a low levels in naive, germinal center and memory B-cells but also expressed in NK cells (at protein level)

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    In Situ
    Assay Products:
     

     
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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 chordates.

    Orthologs for FCRL3 gene from 1/8 species (see all 8)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves FCRL21 Fc receptor-like 2 49.72(n)
    39.89(a)
      425592  NM_001097529.1  NP_001090998.1 


    ENSEMBL Gene Tree for FCRL3 (if available)
    TreeFam Gene Tree for FCRL3 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FCRL3 gene
    FCGR2B2  FCGR1B2  FCGR3B2  FCRL22  FCRLB2  FCRL12  FCRL42  FCRL52  
    FCRLA2  FCGR1A2  FCGR2A2  FCGR3A2  FCER1A2  FCRL62  
    11 SIMAP similar genes for FCRL3 using alignment to 3 protein entries:     FCRL3_HUMAN (see all proteins):
    FCRL1    FCRL2    FLJ00333    FCRL4    FCGR3A    FCRLB
    DKFZp686L20250    FCGR2B    FCGR1A    FCGR3B    Fc-gamma receptor IIIB

    FCRL3 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

    10/468 NCBI SNPs in FCRL3 are shown (see all 468    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 1 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1126557611,2
    --129005595(+) AATATG/AATAGA 1 -- ds50012Minor allele frequency- A:0.09CSA WA 120
    rs168389521,2
    C,F,H,--129006262(+) TCCACT/CGTGAA 1 -- ut31 ese312Minor allele frequency- C:0.09NA NS EA WA 1448
    rs176758621,2
    C,F,H,--129006263(+) CCACTG/ATGAAA 1 -- ut31 ese313Minor allele frequency- A:0.02NA NS 1224
    rs66947651,2
    C,F,A,H,--129006810(+) ACAACG/CTACGC 1 -- int18Minor allele frequency- C:0.07NS EA NA WA 678
    rs75477011,2
    H--129006956(+) TGTTGG/CATTCT 1 -- int14Minor allele frequency- C:0.00NS EA 406
    rs1118770991,2
    F,--129007069(+) TTGCTC/TCTCTG 1 -- int11Minor allele frequency- T:0.04WA 118
    rs120962561,2
    F,--129007224(+) TAAGGC/TCACAT 1 -- int11Minor allele frequency- T:0.15WA 118
    rs1119448421,2
    C,--129007266(+) TGGAGC/GATTGA 1 -- int12Minor allele frequency- G:0.03NA 122
    rs75480951,2
    H--129007376(+) ATTAGG/ATAAGG 1 -- int14Minor allele frequency- A:0.00NS EA 406
    rs412734491,2
    --129008664(+) AATGTC/AATTTT 1 -- int11Minor allele frequency- A:0.01NA 120

    HapMap Linkage Disequilibrium report for FCRL3 (157646271 - 157670775 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for FCRL3: --
    Human Gene Mutation Database (HGMD): FCRL3

    SABiosciences Cancer Mutation PCR Assays
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    (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

    FCRL3 for disorders           About GeneDecksing

    OMIM gene information: 606510    OMIM disorders: --

    UniProtKB/Swiss-Prot: FCRL3_HUMAN, Q96P31
  • Genetic variation in FCRL3 may be a cause of susceptibility to rheumatoid arthritis (RA) [MIM:180300]. It is a
  • systemic inflammatory disease with autoimmune features and a complex genetic component. It primarily affects the
    joints and is characterized by inflammatory changes in the synovial membranes and articular structures, widespread
    fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony
    structures
  • Note=Genetic variation in FCRL3 may influence susceptibility to autoimmune disorders, including Graves
  • disease. Graves disease is an autoimmune disorder associated with overactivity of the thyroid gland and
    hyperthyroidism

    20/29 diseases for FCRL3 (see all 29):    About MalaCards
    systemic lupus erythematosus    lupus erythematosus    rheumatoid arthritis    autoimmune thyroiditis
    arthritis    thyroiditis    graft versus host disease    alopecia areata
    primary biliary cirrhosis    ankylosing spondylitis    rheumatoid arthritis, association with    chronic lymphocytic leukemia
    alopecia    lymphocytic leukemia    spondylitis    behcet's disease
    graves' disease    autoimmune pancreatitis    autoimmune hepatitis    multiple sclerosis

    2 diseases from the University of Copenhagen DISEASES database for FCRL3:
    Rheumatoid arthritis     Graves' disease

    5 Novoseek disease relationships for FCRL3 gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    autoimmune thyroid disease 74.6 5 17117947 (1), 17133579 (1), 17462505 (1)
    autoimmune diseases 71.8 19 17200162 (2), 17462505 (2), 17389014 (1), 17868046 (1) (see all 14)
    rheumatoid arthritis 62.2 16 15838509 (2), 16859508 (1), 17117947 (1), 17200162 (1) (see all 11)
    lupus erythematosus systemic 55.2 7 17117947 (1), 18556175 (1), 19690864 (1), 17462505 (1) (see all 5)
    autoimmunity 42 7 17200162 (2), 15838509 (2), 17462505 (2)

    Human Genome Epidemiology (HuGE) Navigator: FCRL3 (38 documents)

    Export disorders for FCRL3 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 FCRL3 gene, integrated from 9 sources (see all 68):
    (articles sorted by number of sources associating them with FCRL3)
        Utopia: connect your pdf to the dynamic
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    1. Identification of a family of Fc receptor homologs with preferential B cell expression. (PubMed id 11493702)1, 2, 3 Davis R.S....Cooper M.D. (2001)
    2. A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities. (PubMed id 15838509)1, 2, 9 Kochi Y....Yamamoto K. (2005)
    3. Rheumatoid arthritis association with the FCRL3 -169C polymorphism is restricted to PTPN22 1858T-homozygous individuals in a Canadian population. (PubMed id 17133579)1, 2, 9 Newman W.G.... Siminovitch K.A. (2006)
    4. FCRL3 promoter 169 CC homozygosity is associated with susceptibility to rheumatoid arthritis in Dutch Caucasians. (PubMed id 17179172)1, 2, 9 Thabet M.M....Huizinga T.W. (2007)
    5. Epistatic interaction between FCRL3 and NFkappaB1 genes in Spanish patients with rheumatoid arthritis. (PubMed id 16476711)1, 2, 9 Martinez A....Martin J. (2006)
    6. Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity? (PubMed id 16859508)1, 2, 9 Eyre S....Barton A. (2006)
    7. Supportive evidence for a genetic association of the FCRL3 promoter polymorphism with rheumatoid arthritis. (PubMed id 16176992)1, 2, 9 Ikari K....Kamatani N. (2006)
    8. Meta-analysis evidence of a differential risk of the FCRL3 -169T-->C polymorphism in white and East Asian rheumatoid arthritis patients. (PubMed id 17763442)1, 2 Begovich A.B.... Schrodi S.J. (2007)
    9. Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of Graves' disease. (PubMed id 16384851)1, 2 Simmonds M.J....Gough S.C.L. (2006)
    10. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)

    (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)
    About This Section
    Entrez Gene: 115352 HGNC: 18506 AceView: FCRH3 Ensembl:ENSG00000160856 euGenes: HUgn115352
    ECgene: FCRL3 H-InvDB: FCRL3

    (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 FCRL3 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 FCRL3 gene:
    Search GeneIP for patents involving FCRL3

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