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

PLXNC1 Gene

protein-coding   GIFtS: 55
GCID: GC12P094542

plexin C1

 Explore 23 diseases affiliated with
PLXNC1 via our new
 Human Malady Compendium 
Biological research products
for PLXNC1
    

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

Aliases
Plexin C11 2     Plexin (Semaphorin Receptor)2
VESPR1 2 3 5     Plexin-C11
CD2321 2     Receptor For Viral Semaphorin Protein2
Virus-Encoded Semaphorin Protein Receptor2 3     Receptor For Virally-Encoded Semaphorin2
PLXN-C12     CD232 Antigen3

External Ids:    HGNC: 91061   Entrez Gene: 101542   Ensembl: ENSG000001360407   OMIM: 6042595   UniProtKB: O604863   

Export aliases for PLXNC1 gene to outside databases

Previous GC identifers: GC12P094074 GC12P095063 GC12P094475 GC12P093044 GC12P093066 GC12P091610


(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 PLXNC1:
This gene encodes a member of the plexin family. Plexins are transmembrane receptors for semaphorins, a large family of
proteins that regulate axon guidance, cell motility and migration, and the immune response. The encoded protein and
its ligand regulate melanocyte adhesion, and viral semaphorins may modulate the immune response by binding to this
receptor. The encoded protein may be a tumor suppressor protein for melanoma. Alternatively spliced transcript
variants have been observed for this gene. (provided by RefSeq, Jan 2011)

UniProtKB/Swiss-Prot: PLXC1_HUMAN, O60486
Function: Receptor for SEMA7A, for smallpox semaphorin A39R, vaccinia virus semaphorin A39R and for herpesvirus Sema
protein. Binding of semaphorins triggers cellular responses leading to the rearrangement of the cytoskeleton and to
secretion of IL6 and IL8 (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_029419.12  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the PLXNC1 gene promoter:
         E2F-4   E2F-3a   E2F-5   Spz1   Pax-5   E2F-2   GATA-2   E2F   E2F-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidPLXNC1 promoter sequence
   Search SABiosciences Chromatin IP Primers for PLXNC1

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat PLXNC1


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

Entrez Gene cytogenetic band: 12q23.3   Ensembl cytogenetic band:  12q22   HGNC cytogenetic band: 12q23

PLXNC1 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
PLXNC1 gene location

GeneLoc information about chromosome 12         GeneLoc Exon Structure

GeneLoc location for GC12P094542:  view genomic region     (about GC identifiers)

Start:
94,542,499 bp from pter      End:
94,701,451 bp from pter
Size:
158,953 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: PLXC1_HUMAN, O60486 (See protein sequence)
Recommended Name: Plexin-C1 precursor  
Size: 1568 amino acids; 175742 Da
Subunit: Monomer. Homodimer. Interacts with SEMA7A
Subcellular location: Membrane; Single-pass type I membrane protein (Potential)
3 PDB 3D structures from and Proteopedia for PLXNC1:
3KUZ (3D)        3NVN (3D)        3NVQ (3D)    
Secondary accessions: Q59H25

Explore the universe of human proteins at neXtProt for PLXNC1: NX_O60486

Post-translational modifications:

  • N-glycosylated1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_O60486

  • PLXNC1 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_005752.1  
    ENSEMBL proteins: 
     ENSP00000258526   ENSP00000447843   ENSP00000446781   ENSP00000447625   ENSP00000446720  
     ENSP00000439225  
    Reactome Protein details: O60486
    Human Recombinant Protein Products: 
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    Uscn Proteins for PLXNC1

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005622intracellular IEA--
    GO:0005886plasma membrane TAS--
    GO:0016021integral to membrane IEA--


    PLXNC1 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

    PLXNC1 for domains           About GeneDecksing

    5/10 InterPro domains/families (see all 10):
     IPR014756 Ig_E-set
     IPR002165 Plexin_repeat
     IPR002909 IPT_TIG_rcpt
     IPR008936 Rho_GTPase_activation_prot
     IPR013783 Ig-like_fold

    Graphical View of Domain Structure for InterPro Entry O60486

    ProtoNet protein and cluster: O60486

    UniProtKB/Swiss-Prot: PLXC1_HUMAN, O60486
    Similarity: Belongs to the plexin family
    Similarity: Contains 1 Sema domain


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

    Function Summary:

         UniProtKB/Swiss-Prot: PLXC1_HUMAN, O60486
    Function: Receptor for SEMA7A, for smallpox semaphorin A39R, vaccinia virus semaphorin A39R and for herpesvirus Sema
    protein. Binding of semaphorins triggers cellular responses leading to the rearrangement of the cytoskeleton and to
    secretion of IL6 and IL8 (By similarity)

         Genatlas biochemistry entry for PLXNC1:
    plexin C1,calcium-dependent cell adhesion molecule at the neuronal cell surface,receptor for the semaphorin 7A (SEMA7A)

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    hsa-miR-193a-3p hsa-miR-3607-3p hsa-let-7d hsa-miR-219-5p hsa-miR-30d hsa-miR-507 hsa-miR-218 hsa-let-7g
    SwitchGear 3'UTR luciferase reporter plasmidPLXNC1 3' UTR sequence
    Inhib. RNA
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    Gene Ontology (GO): 3 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0004872receptor activity IEA--
    GO:0005102receptor binding TAS9586637
    GO:0005515protein binding IPI--


    PLXNC1 for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for PLXNC1:
     Increased Salmonella enterica  

    Animal Models:
         Mouse knock-out Plxnc1tm1Alk for PLXNC1
         4 MGI mutant phenotypes (inferred from 1 allele(MGI details for Plxnc1):
     cellular  nervous system  normal  vision/eye 

    PLXNC1 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

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Axon guidance
    Axon guidance1.00
    Developmental Biology0.69
    2Other semaphorin interactions
    Other semaphorin interactions1.00
    3Axon guidance
    Axon guidance1.00
    4Sema4D in semaphorin signaling
    Semaphorin interactions0.44

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    4        Reactome Pathways for PLXNC1
        Developmental Biology
    Semaphorin interactions
    Other semaphorin interactions
    Axon guidance


    1         Kegg Pathway  (Kegg details for PLXNC1):
        Axon guidance


    PLXNC1 for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for PLXNC1

    STRING Interaction Network Preview (showing 1 interactants - click image to see more details)

    2 Interacting proteins for PLXNC1 (O604861, 3 ENSP000002585264) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    SEMA7AO753261, 3, ENSP000002619184EBI-2927384,EBI-1753538 I2D: score=3 STRING: ENSP00000261918
    EVM139Q8JL801EBI-2927384,EBI-2927425
    About this table

    Gene Ontology (GO): 4 biological process terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007155cell adhesion TAS9586637
    GO:0007165signal transduction IEA--
    GO:0007275multicellular organismal development ----
    GO:0007411axon guidance TAS--


    PLXNC1 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

    PLXNC1 for compounds           About GeneDecksing

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

    Browse Tocris compounds for PLXNC1
    6 Novoseek chemical compound relationships for PLXNC1 gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    ctab 52 9 18305261 (2), 16275926 (1), 20148037 (1), 12700098 (1)
    vegf 42.6 7 17222790 (1), 19887479 (1), 18363553 (1), 16424390 (1) (see all 6)
    tyrosine 40.6 11 12198496 (2), 18391791 (2), 10520995 (1), 16055703 (1) (see all 9)
    cysteine 7.52 7 15358240 (1), 14597639 (1), 7605632 (1), 12958590 (1)
    calcium 0 2 7605632 (2)
    arginine 0 1 15488183 (1)

    Search CenterWatch for drugs/clinical trials and news about PLXNC1 / PLXC1 

    (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 PLXNC1 gene: 
    NM_005761.2  

    Unigene Cluster for PLXNC1:

    Plexin C1
    Hs.584845  [show with all ESTs]
    Unigene Representative Sequence: NM_005761
    11 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000258526(uc001tdc.3 uc010sut.2 uc009zsv.3) ENST00000546733
    ENST00000551850 ENST00000546659 ENST00000549810 ENST00000549217 ENST00000550080
    ENST00000547057 ENST00000551495 ENST00000545312 ENST00000549187

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    8/45 QIAGEN miScript miRNA Assays for microRNAs that regulate PLXNC1 (see all 45):
    hsa-miR-193a-3p hsa-miR-3607-3p hsa-let-7d hsa-miR-219-5p hsa-miR-30d hsa-miR-507 hsa-miR-218 hsa-let-7g
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    Additional cDNA sequence: 

    AB208934.1 AF030339.1 AF035307.1 AK093735.1 AK124034.1 AK295226.1 AK307920.1 AK308985.1 
    BC029934.1 NR_037687.1 

    9 DOTS entries:

    DT.443808  DT.100019619  DT.405090  DT.95087108  DT.121195352  DT.75154351  DT.121195267  DT.91643805 
    DT.40309667 

    24/131 AceView cDNA sequences (see all 131):

    BE220806 NM_005761 N25656 AI963360 AA702661 AW674021 AI762246 H98855 
    AI393889 BM146532 AA663440 AL708790 AA910509 AA258620 BF222461 N45078 
    AF030339 CA941979 BC029934 N36404 AA476812 AL046443 H79941 AK124034 

    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

    PLXNC1 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: AGTCCTGTGT

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

    About this image

    PLXNC1 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    1 LifeMap In Vivo Development Anatomical Compartment/Cell 
    Tissue Anatomical Compartment CellCategory (developmental path)
    BrainHypothalamusBrain
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 1 LifeMap Cell 
    NameCategory
    Sclerotome cells (Primary Cell)Bone, Cartilage, Somite

    See PLXNC1 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for PLXNC1

    SOURCE GeneReport for Unigene cluster: Hs.584845

    UniProtKB/Swiss-Prot: PLXC1_HUMAN, O60486
    Tissue specificity: Detected in heart, brain, lung, spleen and placenta

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for PLXNC1

    (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 PLXNC1 gene from 7/21 species (see all 21)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Plxnc11 , 5 plexin C11, 5 87.73(n)1
    90.68(a)1
      10 (49.09 cM)5
    547121  NM_018797.21  NP_061267.11 
     947908725 
    chicken
    (Gallus gallus)
    Aves PLXNC11 plexin C1 67.41(n)
    61.84(a)
      417901  XM_416143.3  XP_416143.3 
    lizard
    (Anolis carolinensis)
    Reptilia PLXNC16
    --
    78(a)
    1 ↔ 1
    5(31207421-31230162)
    tropical clawed frog
    (Xenopus tropicalis)
    Amphibia Str.173442 Transcribed sequence with moderate similarity to protein more 76.12(n)    AL773892.2 
    zebrafish
    (Danio rerio)
    Actinopterygii plxnc11 plexin C1 52.2(n)
    43.21(a)
      562273  XM_685667.4  XP_690759.4 
    fruit fly
    (Drosophila melanogaster)
    Insecta plexB6
    plexin B
    17(a)
    1 → many
    4(53104-64404)
    worm
    (Caenorhabditis elegans)
    Secernentea plx-16
    plx-26
    Plexin-2
    17(a)
    15(a)
    possible ortholog
    many → 1
    IV(959452-984392)
    II(14417812-14424815)


    ENSEMBL Gene Tree for PLXNC1 (if available)
    TreeFam Gene Tree for PLXNC1 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for PLXNC1 gene
    PLXNB22  PLXND12  PLXNA32  PLXNA12  PLXNB12  PLXNA22  PLXNB32  PLXNA42  
    17 SIMAP similar genes for PLXNC1 using alignment to 6 protein entries:     PLXC1_HUMAN (see all proteins):
    DKFZp761P19121    PLXND1    PLXNB2    PLXNB1    PLXNA3    PLXNA4
    Nbla00445    MET    PLXNA1    PLXNA2    MM1    PLXNB3
    DKFZp686A04130    DKFZp686D04248    SEMA4A    SEMA4C    SEMA4B

    PLXNC1 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

    10/3038 NCBI SNPs in PLXNC1 are shown (see all 3038    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 12 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs558431361,2
    C--91722107(+) CACCA-/AAGAGAA 1 -- us2k10--------
    rs768822621,2
    --91722107(+) CACCAG/AAGAAC 1 -- us2k11Minor allele frequency- A:0.50CSA 2
    rs1136019161,2
    C,--91722480(+) AGCCCT/CAAGGA 1 -- us2k12Minor allele frequency- C:0.11CSA WA 120
    rs759434071,2
    C,--91722506(+) TGGCCG/ATTACG 1 -- us2k12Minor allele frequency- A:0.12CSA WA 120
    rs748705641,2
    F,--91722629(+) AGATTT/CCAGCA 1 -- us2k14Minor allele frequency- C:0.05CSA WA NA 242
    rs1127381661,2
    --91722806(+) GATGCA/GCAACA 1 -- us2k12Minor allele frequency- G:0.10CSA WA 120
    rs1120439271,2
    --91722823(+) TTTTTA/TATTTC 1 -- us2k12Minor allele frequency- T:0.10CSA WA 120
    rs733685541,2
    C,--91722856(+) AAGGCC/AATACC 1 -- us2k11Minor allele frequency- A:0.50WA 2
    rs1138558271,2
    C,--91723459(+) CAAGAC/TTTCAC 1 -- us2k12Minor allele frequency- T:0.12CSA WA 120
    rs1123644131,2
    --91723567(+) CTTTCG/AGTGGA 1 -- nc-transcript-variant1Minor allele frequency- A:0.50CSA 2

    HapMap Linkage Disequilibrium report for PLXNC1 (94542499 - 94701451 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 6 variations for PLXNC1
         3 CNVs: 49156 49155 66305
         3 Indels: 42517 11638 10698

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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

    PLXNC1 for disorders           About GeneDecksing

    OMIM gene information: 604259    OMIM disorders: --

    20/23 diseases for PLXNC1 (see all 23):    About MalaCards
    melanoma    polycystic kidney and hepatic disease    polycystic kidney disease    acute myeloid leukemia
    smallpox    myeloid leukemia    kidney disease    malignant glioma
    renal cell carcinoma    melanoma metastasis    parkinson's disease    vaccinia
    periodontitis    ovarian cancer    pancreatic cancer    leukemia
    prostate cancer    pancreatitis    hepatitis    prostatitis

    6 Novoseek disease relationships for PLXNC1 gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    arpkd 48.4 1 11919560 (1)
    cancer 28.1 4 14500350 (1), 18275816 (1), 19461072 (1), 19462467 (1)
    metastasis 26.5 2 18987670 (1)
    tumors 14.6 12 19318806 (3), 19887479 (2), 18987670 (2), 15949770 (1) (see all 6)
    metastatic melanoma 13.4 5 19318806 (1), 18987670 (1)
    melanoma 0 11 18987670 (4), 19318806 (2)

    Human Genome Epidemiology (HuGE) Navigator: PLXNC1 (2 documents)

    Export disorders for PLXNC1 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 PLXNC1 gene, integrated from 9 sources (see all 131):
    (articles sorted by number of sources associating them with PLXNC1)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. A poxvirus-encoded semaphorin induces cytokine production from monocytes and binds to a novel cellular semaphorin receptor, VESPR. (PubMed id 9586637)1, 2, 9 Comeau M.R.... Spriggs M.K. (1998)
    2. Structural basis of semaphorin-plexin recognition and viral mimicry from Sema7A and A39R complexes with PlexinC1. (PubMed id 20727575)1, 2 Liu H....He X. (2010)
    3. Plexin C1, a receptor for semaphorin 7a, inactivates cofilin and is a potential tumor suppressor for melanoma progression. (PubMed id 18987670)1, 9 Scott G.A....Fender A. (2009)
    4. Plexins are a large family of receptors for transmembrane, secreted and GPI-anchored semaphorins in vertebrates. (PubMed id 10520995)1, 9 Tamagnone L.... Comoglio P.M. (1999)
    5. The semaphorin 7A receptor Plexin C1 is lost during melanoma metastasis. (PubMed id 19318806)1, 9 Lazova R....Scott G. (2009)
    6. Soluble CD100 functions on human monocytes and immature dendritic cells require plexin C1 and plexin B1, respectively. (PubMed id 15746246)1, 9 Chabbert-de Ponnat I....Boumsell L. (2005)
    7. Molecular profiling of the 'plexinome' in m elanoma and pancreatic cancer. (PubMed id 19462467)1, 9 Balakrishnan A....Tamagnone L. (2009)
    8. Mechanical tension alters semaphorin expression in th e periodontium. (PubMed id 19792857)1, 9 Spencer A.Y. and Lallier T.E. (2009)
    9. Semaphorin 7a promotes spreading and dendricity in human melanocytes through beta1-integrins. (PubMed id 17671519)1, 9 Scott G.A....Fricke A.F. (2008)
    10. Structural basis of Rnd1 binding to plexin Rho GTPase binding domains (RBDs). (PubMed id 21610070)1 Wang H....Park H.W. (2011)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 10154 HGNC: 9106 AceView: PLXNC1 Ensembl:ENSG00000136040 euGenes: HUgn10154
    ECgene: PLXNC1 Kegg: 10154 H-InvDB: PLXNC1

    (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 PLXNC1 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 PLXNC1 gene:
    Search GeneIP for patents involving PLXNC1

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



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