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

CWF19L2 Gene

protein-coding   GIFtS: 45
GCID: GC11M107197

CWF19-Like 2, Cell Cycle Control (S. Pombe)

  See related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
About This Section

Aliases
CWF19-Like 2, Cell Cycle Control (S. Pombe)1 2
CWF19-Like Protein 22

External Ids:    HGNC: 265081   Entrez Gene: 1438842   Ensembl: ENSG000001524047   UniProtKB: Q2TBE03   

Export aliases for CWF19L2 gene to outside databases

Previous GC identifers: GC11M106735 GC11M106702 GC11M103133


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

GeneCards Summary for CWF19L2 Gene: 
CWF19L2 (CWF19-like 2, cell cycle control (S. pombe)) is a protein-coding gene. Diseases associated with CWF19L2 include narcolepsy, and breast cancer. GO annotations related to this gene include catalytic activity. An important paralog of this gene is CWF19L1.


(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 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000011.9  NC_018922.2  NT_033899.8  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the CWF19L2 gene promoter:
         Bach1   Pbx1a   CUTL1   Cdc5   C/EBPalpha   Gfi-1   AREB6   HSF2   Hlf   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 3): CWF19L2 promoter sequence
   Search SABiosciences Chromatin IP Primers for CWF19L2

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat CWF19L2


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

Entrez Gene cytogenetic band: 11q22.3   Ensembl cytogenetic band:  11q22.3   HGNC cytogenetic band: 11q23.1

CWF19L2 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
CWF19L2 gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11M107197:  view genomic region     (about GC identifiers)

Start:
107,197,071 bp from pter      End:
107,328,572 bp from pter
Size:
131,502 bases      Orientation:
minus strand

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB 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 Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: C19L2_HUMAN, Q2TBE0 (See protein sequence)
Recommended Name: CWF19-like protein 2  
Size: 894 amino acids; 103787 Da
Caution: It is uncertain whether Met-1 or Met-5 is the initiator
Sequence caution: Sequence=AAI10440.1; Type=Erroneous initiation; Note=Translation N-terminally extended;
Sequence=AAI10441.1; Type=Erroneous initiation; Note=Translation N-terminally extended; Sequence=AAI10441.1;
Type=Frameshift; Positions=754; Sequence=AAI10442.1; Type=Erroneous initiation; Note=Translation N-terminally
extended; Sequence=AAI10443.2; Type=Erroneous initiation; Note=Translation N-terminally extended;
Sequence=AAI18670.1; Type=Erroneous initiation; Note=Translation N-terminally extended; Sequence=BAB71307.1;
Type=Erroneous initiation; Note=Translation N-terminally extended;
Secondary accessions: A4FU66 A4FU67 A4FU68 Q6PHW1 Q96MI1
Alternative splicing: 3 isoforms:  Q2TBE0-1   Q2TBE0-2   Q2TBE0-3   (No experimental confirmation available. May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay)

Explore the universe of human proteins at neXtProt for CWF19L2: NX_Q2TBE0

Explore proteomics data for CWF19L2 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q2TBE0

  • CWF19L2 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    CWF19L2 Protein Expression
    REFSEQ proteins: NP_689647.2  
    ENSEMBL proteins: 
     ENSP00000282251   ENSP00000411736   ENSP00000434704   ENSP00000387533  

    Human Recombinant Protein Products for CWF19L2: 
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    Cloud-Clone Corp. CLIAs for CWF19L2


    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    3 InterPro protein domains:
     IPR006768 Cwf19-like_C_dom-1
     IPR006767 Cwf19-like_C_dom-2
     IPR011146 HIT-like

    Graphical View of Domain Structure for InterPro Entry Q2TBE0

    ProtoNet protein and cluster: Q2TBE0

    1 Blocks protein domain: IPB006768 Protein similar to CwfJ

    UniProtKB/Swiss-Prot: C19L2_HUMAN, Q2TBE0
    Similarity: Belongs to the CWF19 family


    CWF19L2 for domains           About GeneDecksing


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

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003824catalytic activity IEA--
         
    CWF19L2 for ontologies           About GeneDecksing


    Phenotypes:
         2 GenomeRNAi human phenotypes for CWF19L2:
     Decreased viability of wild-ty  Decreased viability with pacli 

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for CWF19L2 
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       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for CWF19L2 
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    miRNA
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    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat CWF19L2
    2 QIAGEN miScript miRNA Assays for microRNAs that regulate CWF19L2:
    hsa-miR-548a-3p hsa-miR-548e
    SwitchGear 3'UTR luciferase reporter plasmidCWF19L2 3' UTR sequence
    Inhib. RNA
    Products:
        
    Browse for Gene Knock-down Tools from EMD Millipore
    OriGene RNAi products in human, mouse, rat for CWF19L2
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    Gene Editing
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for CWF19L2


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, 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 Oct 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for CWF19L2

    1 Interacting protein for CWF19L2 (Q2TBE03) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    C1QBPQ070213I2D: score=2 
    About this table

    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, 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 CWF19L2 (C19L2)

    Search CenterWatch for drugs/clinical trials and news about CWF19L2 / C19L2

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    Conferences by KenesGroup, 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, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for CWF19L2 gene: 
    NM_152434.2  

    Unigene Cluster for CWF19L2:

    CWF19-like 2, cell cycle control (S. pombe)
    Hs.212140  [show with all ESTs]
    Unigene Representative Sequence: NM_152434
    5 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000282251(uc009yxo.3 uc010rvp.2) ENST00000431778(uc001pjh.4)
    ENST00000532251 ENST00000462890 ENST00000433523
    miRNA
    Products:
         
    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat CWF19L2
    2 QIAGEN miScript miRNA Assays for microRNAs that regulate CWF19L2:
    hsa-miR-548a-3p hsa-miR-548e
    SwitchGear 3'UTR luciferase reporter plasmidCWF19L2 3' UTR sequence
    Inhib. RNA
    Products:
         
    Browse for Gene Knock-down Tools from EMD Millipore
    OriGene RNAi products in human, mouse, rat for CWF19L2
    QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat CWF19L2
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    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat CWF19L2
    Sirion Biotech Customized lentivirus for stable overexpression of CWF19L2 
                         Customized lentivirus expression plasmids for stable overexpression of CWF19L2 
    Primer
    Products:
        
    OriGene qSTAR qPCR primer pairs in human, mouse for CWF19L2
    SABiosciences RT2 qPCR Primer Assay in human, mouse / rat CWF19L2
      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat CWF19L2
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat CWF19L2

    Additional mRNA sequence: 

    AK056905.1 AK126881.1 AK293001.1 AL713739.1 BC016611.1 BC028043.2 BC056241.1 BC070142.1 
    BC107418.1 BC110439.1 BC110440.1 BC110441.1 BC110442.1 BC118669.1 BX647832.1 BX648704.1 
    BX649022.1 

    3 DOTS entries:

    DT.101982120  DT.108856  DT.97807172 

    24/66 AceView cDNA sequences (see all 66):

    AI783699 BG055074 AI805029 BF222365 AI284320 AL713739 AW515353 BC028043 
    BQ876356 AL712586 AK126881 BE645862 BC070142 BX648704 BQ024674 CF994261 
    BM993123 BU633869 BU619197 AA459277 BU951930 CD689043 BG250666 BU951988 

    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

    CWF19L2 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GTTGTTAAGT
    CWF19L2 Expression
    About this image


    See CWF19L2 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for CWF19L2

    SOURCE GeneReport for Unigene cluster: Hs.212140
        SABiosciences Custom PCR Arrays for CWF19L2
    Primer
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    OriGene qSTAR qPCR primer pairs in human, mouse for CWF19L2
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for CWF19L2

    (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 eukaryotes.

    Orthologs for CWF19L2 gene from 10/19 species (see all 19)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Cwf19l21 , 5 CWF19-like 2, cell cycle control (S. pombe)1, 5 81.82(n)1
    74.83(a)1
      9 (2.06 cM)5
    2446721  NM_027545.21  NP_081821.11 
     34040855 
    chicken
    (Gallus gallus)
    Aves CWF19L21 CWF19-like 2, cell cycle control (S. pombe) 67.66(n)
    61.93(a)
      418973  XM_417167.3  XP_417167.3 
    lizard
    (Anolis carolinensis)
    Reptilia CWF19L26
    Uncharacterized protein
    56(a)
    1 ↔ 1
    3(189387188-189618089)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.55142 Xenopus laevis transcribed sequence with weak similarity more 77.91(n)    BU910838.1 
    zebrafish
    (Danio rerio)
    Actinopterygii LOC1005348701 CWF19-like protein 2-like 58.3(n)
    55.82(a)
      100534870  XM_003200092.1  XP_003200140.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG92131 CG9213 44.39(n)
    34.78(a)
      32490  NM_176737.1  NP_788910.1 
    worm
    (Caenorhabditis elegans)
    Secernentea B0361.21 Protein B0361.2 50.32(n)
    38.39(a)
      176034  NM_001025954.3  NP_001021125.1 
    baker's yeast
    (Saccharomyces cerevisiae)
    Saccharomycetes YGR093W6
    Putative protein of unconfirmed function; green fl...
    13(a)
    1 → many
    VII(670388-671911)
    thale cress
    (Arabidopsis thaliana)
    eudicotyledons AT1G562901 CwfJ-like protein 48.39(n)
    35.67(a)
      842082  NM_104508.1  NP_564716.1 
    rice
    (Oryza sativa)
    Liliopsida Os03g07407001 hypothetical protein 47.84(n)
    35.52(a)
      4334057  NM_001057754.1  NP_001051219.1 


    ENSEMBL Gene Tree for CWF19L2 (if available)
    TreeFam Gene Tree for CWF19L2 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for CWF19L2 gene
    CWF19L12  

    CWF19L2 for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, 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

    10/2922 SNPs in CWF19L2 are shown (see all 2922)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 11 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs723945751,2
    C--103166033(+) AACAA-/AA    
       CAGCC
    ATGCA
    1 -- int10--------
    rs105783241,2
    C--107062337(+) GACTC-/A/A   
       A
    /AAA
    AAAAA
    1 -- int10--------
    rs112121591,2
    C,F,A--107196729(+) GCTCAT/CACCTG 1 -- int18Minor allele frequency- C:0.27NA WA EA 368
    rs1850728221,2
    --107196789(+) GAGTTC/GAAGGC 1 -- int10--------
    rs112121601,2
    C,F--107196918(+) TTTACG/AACAAT 1 -- int19Minor allele frequency- A:0.28NA WA EA 506
    rs108907181,2
    C,F,A,H--107196983(+) CCAAAC/TAACCC 1 -- int118Minor allele frequency- T:0.24NS EA NA WA 2336
    rs1904129801,2
    --107197142(+) TAACAA/TAAAGA 1 -- ut310--------
    rs1820517681,2
    --107197162(+) ATACTA/GTATAC 1 -- ut310--------
    rs10460951,2
    C,F,H--107197235(-) ATTTTT/AAAAAA 1 -- ut3111Minor allele frequency- A:0.26NS EA WA NA 786
    rs10460941,2
    C,F,H--107197256(-) CTACTG/CTCTGG 1 -- ut31 ese324Minor allele frequency- C:0.26MN NS EA NA WA 2664

    HapMap Linkage Disequilibrium report for CWF19L2 (107197071 - 107328572 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 10/26 variations for CWF19L2 (see all 26):    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2745047CNV Deletion23290073
    esv2665722CNV Deletion23128226
    dgv239e199CNV Deletion23128226
    esv1000794CNV Deletion20482838
    esv2421980CNV Deletion20811451
    nsv509441CNV Insertion20534489
    nsv898377CNV Loss21882294
    nsv508655CNV Loss20534489
    nsv75CNV Loss15895083
    nsv898374CNV Loss21882294

    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing CWF19L2
    DNA2.0 Custom Variant and Variant Library Synthesis for CWF19L2

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    2 diseases for CWF19L2:    About MalaCards
    narcolepsy    breast cancer


    CWF19L2 for disorders           About GeneDecksing

    Genetic Association Database (GAD): CWF19L2
    Human Genome Epidemiology (HuGE) Navigator: CWF19L2 (3 documents)

    Export disorders for CWF19L2 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 CWF19L2 gene, integrated from 9 sources (see all 15):
    (articles sorted by number of sources associating them with CWF19L2)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2, 3 Ota T.... Sugano S. (2004)
    2. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PubMed id 20379614)1, 4 Rose J.E....Uhl G.R. (2010)
    3. An approach based on a genome-wide association study reveals candidate loci for narcolepsy. (PubMed id 20677014)1, 4 Shimada M....Tokunaga K. (2010)
    4. Genome-wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expression, and germline haplotypes in breast cancer patients. (PubMed id 18398821)1, 4 Nordgard S.H....Kristensen V.N. (2008)
    5. Initial characterization of the human central proteome. (PubMed id 21269460)2 Burkard T.R.... Colinge J. (2011)
    6. System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation. (PubMed id 21406692)2 Rigbolt K.T....Blagoev B. (2011)
    7. Interactions of pathological hallmark proteins: tubul in polymerization promoting protein/p25, beta-amyloid, and alpha-synuclein. (PubMed id 21832049)1 OlA!h J....OvA!di J. (2011)
    8. Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions. (PubMed id 19690332)2 Mayya V.... Han D.K. (2009)
    9. A quantitative atlas of mitotic phosphorylation. (PubMed id 18669648)2 Dephoure N.... Gygi S.P. (2008)
    10. Genome-wide association with select biomarker traits in the Framingham Heart Study. (PubMed id 17903293)4 Benjamin E.J....Vasan R.S. (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)
    About This Section
    Entrez Gene: 143884 HGNC: 26508 AceView: CWF19L2 Ensembl:ENSG00000152404 euGenes: HUgn143884
    ECgene: CWF19L2 H-InvDB: CWF19L2

    (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 CWF19L2 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 CWF19L2 gene:
    Search GeneIP for patents involving CWF19L2

    GeneCards and IP:
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