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

CPXM2 Gene

protein-coding   GIFtS: 52
GCID: GC10M125462

Carboxypeptidase X (M14 Family), Member 2

Alzheimer's & Parkinson's Diseases Congress
  See related disease
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
Carboxypeptidase X (M14 Family), Member 21 2     Carboxypeptidase Hlo2
Cytosolic Carboxypeptidase1 2     Carboxypeptidase-Like Protein X22
4632435C11Rik2     Inactive Carboxypeptidase-Like Protein X22
CPX22     EC 3.4.178
UNQ6762     EC 3.4.17.38

External Ids:    HGNC: 269771   Entrez Gene: 1195872   Ensembl: ENSG000001218987   UniProtKB: Q8N4363   

Export aliases for CPXM2 gene to outside databases

Previous GC identifers: GC10M125495 GC10M119120


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

GeneCards Summary for CPXM2 Gene: 
CPXM2 (carboxypeptidase X (M14 family), member 2) is a protein-coding gene. Diseases associated with CPXM2 include alzheimer's disease. GO annotations related to this gene include metallocarboxypeptidase activity and zinc ion binding. An important paralog of this gene is CPZ.

UniProtKB/Swiss-Prot: CPXM2_HUMAN, Q8N436
Function: May be involved in cell-cell interactions




(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_000010.10  NT_030059.13  NC_018921.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the CPXM2 gene promoter:
         Max1   TBP   RFX1   CUTL1   GATA-2   S8   FOXC1   TFIID   RSRFC4   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidCPXM2 promoter sequence
   Search SABiosciences Chromatin IP Primers for CPXM2

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat CPXM2


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

Entrez Gene cytogenetic band: 10q26.13   Ensembl cytogenetic band:  10q26.13   HGNC cytogenetic band: 10q26

CPXM2 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
CPXM2 gene location

GeneLoc information about chromosome 10         GeneLoc Exon Structure

GeneLoc location for GC10M125462:  view genomic region     (about GC identifiers)

Start:
125,465,723 bp from pter      End:
125,699,783 bp from pter
Size:
234,061 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: CPXM2_HUMAN, Q8N436 (See protein sequence)
Recommended Name: Inactive carboxypeptidase-like protein X2 precursor  
Size: 756 amino acids; 85870 Da
Subcellular location: Secreted (Probable)
Caution: Although related to peptidase M14 family, lacks the active sites residues and zinc-binding sites,
suggesting that it has no carboxypeptidase activity

Explore the universe of human proteins at neXtProt for CPXM2: NX_Q8N436

Explore proteomics data for CPXM2 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q8N436

  • 2 DME Specific Peptides for CPXM2 (Q8N436)
     GDYWRLL  YLHTNCFE 

    CPXM2 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    CPXM2 Protein Expression
    REFSEQ proteins: NP_937791.2  
    ENSEMBL proteins: 
     ENSP00000241305  

    Human Recombinant Protein Products for CPXM2: 
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    Novus Biologicals CPXM2 Protein
    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates 
    Browse ProSpec Recombinant Proteins
    Browse Proteins at Cloud-Clone Corp. 

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005615extracellular space IDA--
    GO:0031012colocalizes with extracellular matrix IDA--

    CPXM2 for ontologies           About GeneDecksing



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    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    IUPHAR Guide to PHARMACOLOGY protein family classification: Carboxypeptidase X (M14 family), member 2 
    Metallocarboxypeptidases

    5 InterPro protein domains:
     IPR008969 CarboxyPept-like_regulatory
     IPR014766 CarboxyPept_regulatory_dom
     IPR008979 Galactose-bd-like
     IPR000834 Peptidase_M14
     IPR000421 Coagulation_fac_5/8-C_type_dom

    Graphical View of Domain Structure for InterPro Entry Q8N436

    ProtoNet protein and cluster: Q8N436

    2 Blocks protein domains:
    IPB000421 Coagulation factor 5/8 type C domain (FA58C)
    IPB000834 Zinc carboxypeptidase A metalloprotease (M14)


    UniProtKB/Swiss-Prot: CPXM2_HUMAN, Q8N436
    Similarity: Belongs to the peptidase M14 family
    Similarity: Contains 1 F5/8 type C domain


    CPXM2 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

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: CPXM2_HUMAN, Q8N436
    Function: May be involved in cell-cell interactions

         Enzyme Numbers (IUBMB): EC 3.4.172 EC 3.4.17.32

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0004181metallocarboxypeptidase activity IEA--
    GO:0008270zinc ion binding IEA--
         
    CPXM2 for ontologies           About GeneDecksing


    Phenotypes:
         1 MGI phenotypic allele for Cpxm2 (no phenotypes)

    CPXM2 for phenotypes           About GeneDecksing

    Animal Models:
         MGI mouse knock-out Cpxm2tm1Lex for CPXM2

       inGenious Targeting Laboratory - Custom generated mouse model solutions for CPXM2 
       inGenious Targeting Laboratory - Custom generated inducible mouse model solutions for CPXM2

       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for CPXM2 
       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for CPXM2 

    miRNA
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    4 QIAGEN miScript miRNA Assays for microRNAs that regulate CPXM2:
    hsa-miR-183* hsa-miR-653 hsa-miR-1261 hsa-miR-1827
    SwitchGear 3'UTR luciferase reporter plasmidCPXM2 3' UTR sequence
    Inhib. RNA
    Products:
        
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    Gene Editing
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    Clone
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    Sino Biological Human cDNA Clone for CPXM2
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                         Customized lentivirus expression plasmids for stable overexpression of CPXM2 

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    In Situ Assay
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for CPXM2


    (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 CPXM2

    1 Interacting protein for CPXM2 (Q8N4363) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    SMAD9O151983I2D: score=1 
    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:0006508proteolysis IEA--
    GO:0007155cell adhesion IEA--

    CPXM2 for ontologies           About GeneDecksing



    (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 CPXM2

    Search CenterWatch for drugs/clinical trials and news about CPXM2

    (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 CPXM2 gene: 
    NM_198148.2  

    Unigene Cluster for CPXM2:

    Carboxypeptidase X (M14 family), member 2
    Hs.656887  [show with all ESTs]
    Unigene Representative Sequence: AY358565
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000368854(uc001lhj.3) ENST00000241305(uc001lhk.1) ENST00000481775


    miRNA
    Products:
         
    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat CPXM2
    4 QIAGEN miScript miRNA Assays for microRNAs that regulate CPXM2:
    hsa-miR-183* hsa-miR-653 hsa-miR-1261 hsa-miR-1827
    SwitchGear 3'UTR luciferase reporter plasmidCPXM2 3' UTR sequence
    Inhib. RNA
    Products:
         
    Browse for Gene Knock-down Tools from EMD Millipore
    OriGene RNAi products in human, mouse, rat for CPXM2
    QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat CPXM2
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    DNA2.0 Custom Codon Optimized Gene Synthesis Service for CPXM2
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat CPXM2
    Sirion Biotech Customized lentivirus for stable overexpression of CPXM2 
                         Customized lentivirus expression plasmids for stable overexpression of CPXM2 
    Primer
    Products:
        
    OriGene qPCR primer pairs and template standards for CPXM2
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat CPXM2
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat CPXM2

    Additional mRNA sequence: 

    AK296365.1 AK300506.1 AK304023.1 AK304814.1 AL833732.1 AY358565.1 BC036789.1 BC137492.1 
    BC146862.1 

    7 DOTS entries:

    DT.313496  DT.97840995  DT.100775993  DT.121263860  DT.40217909  DT.91814375  DT.91684305 

    24/100 AceView cDNA sequences (see all 100):

    AI300011 BM727787 AA045145 BQ007818 AY358565 BM707193 BM717146 W81558 
    W81559 AW024746 CA312019 AA045254 BQ018181 AI366508 BC036789 AI041966 
    NM_198148 AI143223 AW513612 BI492793 AA399633 AW183078 W95103 AI800887 

    GeneLoc Exon Structure

    5 Alternative Splicing Database (ASD) splice patterns (SP) for CPXM2    About this scheme

    ExUns: 1 ^ 2 ^ 3 ^ 4a · 4b ^ 5 ^ 6a · 6b ^ 7 ^ 8a · 8b ^ 9 ^ 10 ^ 11 ^ 12 ^ 13a · 13b ^ 14 ^ 15 ^ 16 ^ 17 ^ 18
    SP1:        -           -     -           -     -                                         -           -                                 
    SP2:                    -     -           -     -                                                                                       
    SP3:                                      -     -                                                                                       
    SP4:                    -     -                                                                                                         
    SP5:                                                                                                                                    


    ECgene alternative splicing isoforms for CPXM2

    (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

    CPXM2 expression in normal human tissues (normalized intensities)      CPXM2 embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GGTTGGCCTC
    CPXM2 Expression
    About this image


    CPXM2 expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/14 selected tissues (see all 14) fully expand
     
     Fibroblast
             X-gene Foreskin Fibroblasts   
     
     Mesenchymal Stem Cells (Integumentary System)    fully expand to see all 4 entries
             Human Mesenchymal Stem Cells (hMSC)-1   
     
     Dermis (Uncategorized)    fully expand to see all 4 entries
             Human Dermal Fibroblasts-adult (HDF-a)   
     
     Cartilage (Muscoskeletal System)    fully expand to see all 2 entries
             Normal Human Articular chondrocytes (NHAC)   
     
     Smooth Muscle (Muscoskeletal System)
             Coronary Artery Smooth Muscle Cells (CASMC)   

    See CPXM2 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for CPXM2

    SOURCE GeneReport for Unigene cluster: Hs.656887
        SABiosciences Custom PCR Arrays for CPXM2
    Primer
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for CPXM2

    (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 CPXM2 gene from 4/11 species (see all 11)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Cpxm21 , 5 carboxypeptidase X 2 (M14 family)1, 5 85.61(n)1
    89.67(a)1
      7 (75.60 cM)5
    559871  NM_018867.51  NP_061355.31 
     1320428165 
    chicken
    (Gallus gallus)
    Aves CPXM21 carboxypeptidase X (M14 family), member 2 75.8(n)
    81.3(a)
      423951  XM_421810.3  XP_421810.3 
    lizard
    (Anolis carolinensis)
    Reptilia CPXM26
    Uncharacterized protein
    89(a)
    1 ↔ 1
    3(60819892-60888936)
    zebrafish
    (Danio rerio)
    Actinopterygii LOC1003333511 inactive carboxypeptidase-like protein X2-like 68.03(n)
    67.89(a)
      100333351  XM_002664050.2  XP_002664096.2 


    ENSEMBL Gene Tree for CPXM2 (if available)
    TreeFam Gene Tree for CPXM2 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for CPXM2 gene
    CPZ2  CPE2  AEBP12  CPN12  CPD2  CPM2  CPXM12  
    9 SIMAP similar genes for CPXM2 using alignment to 3 protein entries:     CPXM2_HUMAN (see all proteins):
    DKFZp666J235    CPXM1    F8C    CPE    AEBP1    CPZ
    CPN1    CPM    CNTNAP2

    CPXM2 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

    10/3376 SNPs in CPXM2 are shown (see all 3376)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 10 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1466339901,2
    C,Funtested1125557567(+) TATGCG/AGATGT 2 /R /C mis11Minor allele frequency- A:0.00NA 4552
    rs1444664071,2
    --125504735(+) TCTGCC/TTACCT 1 -- int10--------
    rs122444401,2
    --125504741(+) tacctC/Tggcct 1 -- int10--------
    rs1885617491,2
    --125504753(+) CCAAAC/GTGCTG 1 -- int10--------
    rs1923520311,2
    C--125504823(+) GTTATC/GACAGA 1 -- int10--------
    rs79182571,2
    C,F,A,H--125504915(+) AAGCTG/ATATGA 1 -- int127Minor allele frequency- A:0.25NS EA NA WA CSA 2763
    rs1849438041,2
    --125504916(+) AGCTGG/TATGAG 1 -- int10--------
    rs1866534131,2
    C--125504983(+) ACAAGA/TGTCTC 1 -- int10--------
    rs1136216181,2
    C--125505169(+) ATTTGC/TTTTAT 1 -- ut312Minor allele frequency- T:0.03NA 122
    rs32145381,2
    C--125505174(-) AAAAA-/ATAAAG 1 -- ut31 trp30--------

    HapMap Linkage Disequilibrium report for CPXM2 (125465723 - 125699783 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 10 variations for CPXM2:    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2742550CNV Deletion23290073
    esv2742528CNV Deletion23290073
    esv2742539CNV Deletion23290073
    esv2742517CNV Deletion23290073
    esv2220029CNV Deletion18987734
    esv2742506CNV Deletion23290073
    nsv820023CNV Loss19587683
    esv27822CNV Loss19812545
    nsv25320CNV Loss16902084
    nsv832011CNV Gain+Loss17160897


    Human Gene Mutation Database (HGMD): CPXM2
    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing CPXM2
    DNA2.0 Custom Variant and Variant Library Synthesis for CPXM2

    (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 CPXM2:    About MalaCards
    alzheimer's disease    


    CPXM2 for disorders           About GeneDecksing


    Congresses - knowledge worth sharing:  
    Alzheimer's & Parkinson's Diseases Congress (ADPD) 18 - 22 March 2015
    Genetic Association Database (GAD): CPXM2
    Human Genome Epidemiology (HuGE) Navigator: CPXM2 (2 documents)

    Export disorders for CPXM2 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 CPXM2 gene integrated from 9 sources:
    (articles sorted by number of sources associating them with CPXM2)
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    1. The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. (PubMed id 12975309)1, 2, 3 Clark H.F.... Gray A.M. (2003)
    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. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. (PubMed id 16385451)1, 4 Grupe A....Goate A. (2006)
    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. Functional proteomics mapping of a human signaling pathway. (PubMed id 15231748)1 Colland F....Gauthier J.M. (2004)
    6. The DNA sequence and comparative analysis of human chromosome 10. (PubMed id 15164054)2 Deloukas P.... Rogers J. (2004)
    7. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (2002)
    8. Identification of mouse CPX-2, a novel member of the metallocarboxypeptidase gene family: cDNA cloning, mRNA distribution, and protein expression and characterization. (PubMed id 9809751)1 Xin X....Fricker L.D. (1998)

    (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: 119587 HGNC: 26977 AceView: CPXM2 Ensembl:ENSG00000121898 euGenes: HUgn119587
    ECgene: CPXM2 H-InvDB: CPXM2

    (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 CPXM2 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 CPXM2 gene:
    Search GeneIP for patents involving CPXM2

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



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