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

FGFR1OP2 Gene

protein-coding   GIFtS: 52
GCID: GC12P027091

FGFR1 oncogene partner 2

 Explore 11 diseases affiliated with
FGFR1OP2 via our new
 Human Malady Compendium 
Biological research products
for FGFR1OP2
    

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

Aliases
FGFR1 Oncogene Partner 21 2
DKFZp564O18631
HSPC123-Like1
WIT3.02
Fibroblast Growth Factor Receptor 1 Oncogene Partner 22
Wound Inducible Transcript 3.02

External Ids:    HGNC: 230981   Entrez Gene: 261272   Ensembl: ENSG000001117907   OMIM: 6088585   UniProtKB: Q9NVK53   

Export aliases for FGFR1OP2 gene to outside databases

Previous GC identifers: GC00U912750 GC12P026983 GC12P026984 GC12P026861


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

UniProtKB/Swiss-Prot: FGOP2_HUMAN, Q9NVK5
Function: May be involved in wound healing pathway (By similarity)




(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_009714.17  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FGFR1OP2 gene promoter:
         Elk-1   AML1a   Nkx2-2   HSF1 (long)   HNF-3beta   GATA-2   Egr-4   FAC1   HFH-1   HSF1short   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): FGFR1OP2 promoter sequence
   Search SABiosciences Chromatin IP Primers for FGFR1OP2

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat FGFR1OP2


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

Entrez Gene cytogenetic band: 12p11.23   Ensembl cytogenetic band:  12p11.23   HGNC cytogenetic band: 12p12.1

FGFR1OP2 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FGFR1OP2 gene location

GeneLoc information about chromosome 12         GeneLoc Exon Structure

GeneLoc location for GC12P027091:  view genomic region     (about GC identifiers)

Start:
27,091,305 bp from pter      End:
27,119,583 bp from pter
Size:
28,279 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: FGOP2_HUMAN, Q9NVK5 (See protein sequence)
Recommended Name: FGFR1 oncogene partner 2  
Size: 253 amino acids; 29426 Da
Subcellular location: Cytoplasm (By similarity)
Sequence caution: Sequence=AAF29087.1; Type=Frameshift; Positions=61, 67, 72, 91; Sequence=CAB56012.1; Type=Frameshift;
Positions=189;
Secondary accessions: Q6R955 Q8N5L7 Q9P034 Q9UFK8
Alternative splicing: 3 isoforms:  Q9NVK5-1   Q9NVK5-2   Q9NVK5-3   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for FGFR1OP2: NX_Q9NVK5

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q9NVK5

  • FGFR1OP2 Protein expression data from MOPED and PaxDb:    About this image 
    FGFR1OP2 Protein Expression
    REFSEQ proteins (3 alternative transcripts): 
    NP_001165358.1  NP_001165359.1  NP_056448.1  

    ENSEMBL proteins: 
     ENSP00000229395   ENSP00000441144   ENSP00000437556   ENSP00000323763  
    Reactome Protein details: Q9NVK5
    Human Recombinant Protein Products for FGFR1OP2: 
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    Novus Biologicals FGFR1OP2 Lysate
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    Uscn Proteins for FGFR1OP2

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005737cytoplasm ----
    GO:0005829cytosol TAS--

    FGFR1OP2 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

    FGFR1OP2 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR008555 SIKE

    Graphical View of Domain Structure for InterPro Entry Q9NVK5

    ProtoNet protein and cluster: Q9NVK5

    UniProtKB/Swiss-Prot: FGOP2_HUMAN, Q9NVK5
    Similarity: Belongs to the SIKE family


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

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: FGOP2_HUMAN, Q9NVK5
    Function: May be involved in wound healing pathway (By similarity)

         Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0042803protein homodimerization activity IEA--
         
    FGFR1OP2 for ontologies           About GeneDecksing


    Phenotypes:
         1 GenomeRNAi human phenotype for FGFR1OP2:
     Increased gamma-H2AX phosphory 

    Animal Models:
       inGenious Targeting Laboratory - Customizable classic, inducible, and humanized mouse model solutions for FGFR1OP2 

    miRNA
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    hsa-miR-495 hsa-miR-520d-5p hsa-miR-1297 hsa-miR-1244 hsa-miR-7-1* hsa-miR-558 hsa-miR-129-3p hsa-miR-129*
    SwitchGear 3'UTR luciferase reporter plasmidFGFR1OP2 3' UTR sequence
    Inhib. RNA
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FGFR1OP2


    (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
    1Signaling by FGFR1 mutants
    Signaling by FGFR1 mutants1.00
    Signaling by FGFR1 fusion mutants0.63
    Signaling by FGFR mutants0.67
    FGFR1 fusion proteins recruit PIK3R10.37
    2Disease
    Disease1.00
    3Signaling by FGFR
    Signaling by FGFR in disease0.91

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    5/6        Reactome Pathways for FGFR1OP2 (see all 6)
        Signaling by FGFR mutants
    Signaling by FGFR1 fusion mutants
    Signaling by FGFR in disease
    Signaling by FGFR1 mutants
    Disease



    FGFR1OP2 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for FGFR1OP2

    STRING Interaction Network Preview (showing 5 interactants - click image to see 20)

    5/21 Interacting proteins for FGFR1OP2 (Q9NVK53 ENSP000002293954) via UniProtKB, MINT, STRING, and/or I2D (see all 21)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    STK24Q9Y6E03, ENSP000003657304I2D: score=2 STRING: ENSP00000365730
    TRAF3IP3Q9Y2283, ENSP000000103384I2D: score=2 STRING: ENSP00000010338
    ZRANB1Q9UGI03, ENSP000003526764I2D: score=2 STRING: ENSP00000352676
    PPP2R1AP301533, ENSP000003248044I2D: score=1 STRING: ENSP00000324804
    STRNO438153, ENSP000002639184I2D: score=1 STRING: ENSP00000263918
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0009611response to wounding ----
    GO:0042060wound healing IEA--

    FGFR1OP2 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
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for FGFR1OP2
    Search CenterWatch for drugs/clinical trials and news about FGFR1OP2 / FGOP2 

    (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, Sirion Biotech, 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 FGFR1OP2 gene (3 alternative transcripts): 
    NM_001171887.1  NM_001171888.1  NM_015633.2  

    Unigene Cluster for FGFR1OP2:

    FGFR1 oncogene partner 2
    Hs.591162  [show with all ESTs]
    Unigene Representative Sequence: NM_015633
    6 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000229395(uc001rhm.3 uc001rhn.3) ENST00000544111 ENST00000395941
    ENST00000546072(uc001rhl.3) ENST00000327214 ENST00000538172

    miRNA
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    hsa-miR-495 hsa-miR-520d-5p hsa-miR-1297 hsa-miR-1244 hsa-miR-7-1* hsa-miR-558 hsa-miR-129-3p hsa-miR-129*
    SwitchGear 3'UTR luciferase reporter plasmidFGFR1OP2 3' UTR sequence
    Inhib. RNA
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    Additional cDNA sequence: 

    AF086411.1 AF161472.1 AK001534.1 AK094888.1 AL117545.1 AL117608.1 AY506561.1 BC032143.2 

    9 DOTS entries:

    DT.100646168  DT.210166  DT.100042064  DT.100751357  DT.442919  DT.40118670  DT.95200942  DT.95087970 
    DT.95088329 

    24/200 AceView cDNA sequences (see all 200):

    BX395292 AA262972 AK001534 BU787452 AA384443 BX507394 AA730013 Z99418 
    AW571785 BE894371 CB104864 BQ694324 BU661007 CB158376 BP342418 BC032143 
    BM782815 AL699273 W74643 BU739995 AF086411 BX489960 BQ435164 CD678165 

    GeneLoc Exon Structure

    5/7 Alternative Splicing Database (ASD) splice patterns (SP) for FGFR1OP2 (see all 7)    About this scheme

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


    ECgene alternative splicing isoforms for FGFR1OP2

    (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

    FGFR1OP2 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TTTAAAGACA
    FGFR1OP2 Expression
    About this image
    See FGFR1OP2 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FGFR1OP2

    SOURCE GeneReport for Unigene cluster: Hs.591162

    UniProtKB/Swiss-Prot: FGOP2_HUMAN, Q9NVK5
    Tissue specificity: Expressed in bone marrow, spleen and thymus

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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 animals.

    Orthologs for FGFR1OP2 gene from 6/22 species (see all 22)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Fgfr1op21 , 5 FGFR1 oncogene partner 21, 5 89.06(n)1
    98.81(a)1
      6 (77.70 cM)5
    675291  NM_026218.21  NP_080494.11 
     1465772035 
    chicken
    (Gallus gallus)
    Aves FGFR1OP21 FGFR1 oncogene partner 2 82.02(n)
    93.95(a)
      418214  NM_001007855.1  NP_001007856.1 
    lizard
    (Anolis carolinensis)
    Reptilia FGFR1OP26
    --
    81(a)
    1 ↔ 1
    5(91093308-91099956)
    African clawed frog
    (Xenopus laevis)
    Amphibia MGC529632 hypothetical protein MGC52963 74(n)    BC041504.1 
    zebrafish
    (Danio rerio)
    Actinopterygii wufj17h042 wufj17h04 76.31(n)   335511  BC053266.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG101581 CG10158 47.67(n)
    34.08(a)
      33971  NM_135240.3  NP_609084.1 


    ENSEMBL Gene Tree for FGFR1OP2 (if available)
    TreeFam Gene Tree for FGFR1OP2 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FGFR1OP2 gene
    SIKE12  
    1 SIMAP similar gene for FGFR1OP2 using alignment to 2 protein entries:     FGOP2_HUMAN (see all proteins):
    SIKE1

    FGFR1OP2 for paralogs           About GeneDecksing


    3 Pseudogenes.org Pseudogenes for FGFR1OP2
    PGOHUM00000239609 PGOHUM00000239768 PGOHUM00000248548


    (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

    10/485 NCBI SNPs in FGFR1OP2 are shown (see all 485    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 12 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1482927121,2
    --27089447(+) CATAT-/AAAAAT 4 -- us2k1 int10--------
    rs1147657851,2
    C,F--27089484(+) AAAATC/AATGAT 4 -- us2k1 int11Minor allele frequency- A:0.03WA 118
    rs1505130151,2
    C--27089786(+) GTACAC/TAACAT 4 -- us2k1 int10--------
    rs116115631,2
    C,F,H--27089806(+) TTTCTA/CATTTT 4 -- us2k1 int16Minor allele frequency- C:0.02NA 152
    rs1912676291,2
    --27089843(+) AAGACA/TTGGTA 4 -- us2k1 int10--------
    rs1834411791,2
    --27090027(+) GTCAGA/TGGGAA 4 -- us2k1 int10--------
    rs1885529441,2
    --27090029(+) CAGAGC/GGAAAC 4 -- us2k1 int10--------
    rs1909533141,2
    --27090049(+) TTTAAA/TTGTAT 4 -- us2k1 int10--------
    rs1418643731,2
    --27090230(+) GGAAAC/GAGGAG 4 -- us2k1 int10--------
    rs1831786181,2
    --27090376(+) TAGAGC/TAGAAA 4 -- int1 us2k10--------

    HapMap Linkage Disequilibrium report for FGFR1OP2 (27091305 - 27119583 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for FGFR1OP2: --

    SABiosciences Cancer Mutation PCR Assays
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing FGFR1OP2
    DNA2.0 Custom Variant and Variant Library Synthesis for FGFR1OP2

    (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

    FGFR1OP2 for disorders           About GeneDecksing

    OMIM gene information: 608858    OMIM disorders: --

    UniProtKB/Swiss-Prot: FGOP2_HUMAN, Q9NVK5
  • Note=A chromosomal aberration involving FGFR1OP2 may be a cause of stem cell myeloproliferative disorder
  • (MPD). Insertion ins(12;8)(p11;p11p22) with FGFR1. MPD is characterized by myeloid hyperplasia, eosinophilia and
    T-cell or B-cell lymphoblastic lymphoma. In general it progresses to acute myeloid leukemia. The fusion protein
    FGFR1OP2-FGFR1 may exhibit constitutive kinase activity and be responsible for the transforming activity

    11 diseases for FGFR1OP2:    About MalaCards
    cerebral cavernous malformations    cavernous malformation    cerebral cavernous malformations 3    stem cell leukemia
    acute myeloid leukemia    myeloproliferative disorder    myeloid leukemia    lymphoblastic lymphoma
    t-cell leukemia    cerebritis    leukemia

    1 disease from the University of Copenhagen DISEASES database for FGFR1OP2:
    Stem cell leukemia
    Human Genome Epidemiology (HuGE) Navigator: FGFR1OP2 (2 documents)

    Export disorders for FGFR1OP2 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 FGFR1OP2 gene, integrated from 9 sources (see all 20):
    (articles sorted by number of sources associating them with FGFR1OP2)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Identification of a novel gene, FGFR1OP2, fused to FGFR1 in 8p11 myeloproliferative syndrome. (PubMed id 15034873)1, 2, 3, 9 Grand E.K.... Cross N.C.P. (2004)
    2. Phosphotyrosine profiling identifies the KG-1 cell line as a model for the study of FGFR1 fusions in acute myeloid leukemia. (PubMed id 16946300)1, 2, 9 Gu T.-L....Polakiewicz R.D. (2006)
    3. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    4. Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells. (PubMed id 11042152)1, 2 Zhang Q.-H.... Chen Z. (2000)
    5. A census of human soluble protein complexes. (PubMed id 22939629)1 Havugimana P.C....Emili A. (2012)
    6. Sp1 phosphorylation by cyclin-dependent kinase 1/cycli n B1 represses its DNA-binding activity during mitosis in cancer cells. (PubMed id 22266860)1 Chuang J.Y....Hung J.J. (2012)
    7. Association between FGFR1OP2/wit3.0 polymorphisms and residual ridge resorption of mandible in Korean population. (PubMed id 22880093)1 Kim J.H....Lee J. (2012)
    8. A genetic association study of single nucleotide poly morphisms in FGFR1OP2/wit3.0 and long-term atrophy of edentulous mandible. (PubMed id 21283824)1 Suwanwela J....Nishimura I. (2011)
    9. Mass spectrometric analysis of lysine ubiquitylation r eveals promiscuity at site level. (PubMed id 21139048)1 Danielsen J.M....Nielsen M.L. (2011)
    10. A large-scale candidate gene association study of age at menarche and age at natural menopause. (PubMed id 20734064)1 He C....Hunter D.J. (2010)

    (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: 26127 HGNC: 23098 AceView: FGFR1OP2 Ensembl:ENSG00000111790 euGenes: HUgn26127
    ECgene: FGFR1OP2 H-InvDB: FGFR1OP2

    (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 FGFR1OP2 Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for FGFR1OP2 Genetics and Cytogenetics in Oncology and Haematology

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for FGFR1OP2 gene:
    Search GeneIP for patents involving FGFR1OP2

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



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