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

PLXNB3 Gene

protein-coding   GIFtS: 61
GCID: GC0XP153029

plexin B3


(Previous symbol: PLXN6)
 Explore 5 diseases affiliated with
PLXNB3 via our new
 Human Malady Compendium 
Biological research products
for PLXNB3
    

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

Aliases
Plexin B31 2     Plexin 62
PLXN61 2 3 5     Plexin-B31
PLEXB31 2     KIAA12063
PLEXR1 2     

External Ids:    HGNC: 91051   Entrez Gene: 53652   Ensembl: ENSG000001987537   OMIM: 3002145   UniProtKB: Q9ULL43   

Export aliases for PLXNB3 gene to outside databases

Previous GC identifers: GC0XP147167 GC0XP149484 GC0XP150615 GC0XP151497 GC0XP152550 GC0XP152682 GC0XP141686


(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 PLXNB3:
The protein encoded by this gene is a member of the plexin family. It functions as a receptor for semaphorin 5A, and
plays a role in axon guidance, invasive growth and cell migration. Alternatively spliced transcript variants encoding
different isoforms have been found for this gene. (provided by RefSeq, Sep 2009)

UniProtKB/Swiss-Prot: PLXB3_HUMAN, Q9ULL4
Function: Receptor for SEMA5A that plays a role in axon guidance, invasive growth and cell migration. Stimulates
neurite outgrowth and mediates Ca(2+)/Mg(2+)-dependent cell aggregation. In glioma cells, SEMA5A stimulation of PLXNB3
results in the disassembly of F-actin stress fibers, disruption of focal adhesions and cellular collapse as well as
inhibition of cell migration and invasion through ARHGDIA-mediated inactivation of RAC1

Gene Wiki entry for PLXNB3


(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_000023.10  NC_018934.1  NT_167198.1  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the PLXNB3 gene promoter:
         POU2F2 (Oct-2.1)   Oct-B1   Egr-3   oct-B3   oct-B2   Nkx2-5   POU2F2   POU2F1   COMP1   POU2F1a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidPLXNB3 promoter sequence
   Search SABiosciences Chromatin IP Primers for PLXNB3

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat PLXNB3


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

Entrez Gene cytogenetic band: Xq28   Ensembl cytogenetic band:  Xq28   HGNC cytogenetic band: Xq28

PLXNB3 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
PLXNB3 gene location

GeneLoc information about chromosome X         GeneLoc Exon Structure

GeneLoc location for GC0XP153029:  view genomic region     (about GC identifiers)

Start:
153,029,651 bp from pter      End:
153,044,801 bp from pter
Size:
15,151 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: PLXB3_HUMAN, Q9ULL4 (See protein sequence)
Recommended Name: Plexin-B3 precursor  
Size: 1909 amino acids; 206847 Da
Subunit: Interacts (via cytoplasmic domain) with RAC1 and ARHGDIA (By similarity). Binds MET and MST1R. Interacts (via
cytoplasmic domain) with FSCN1. Interacts with RIT2/RIN. May form homodimers (via Sema domain)
Subcellular location: Cell membrane; Single-pass type I membrane protein. Note=Colocalizes with RIT2/RIN at the plasma
membrane
Sequence caution: Sequence=BAA86520.1; Type=Erroneous initiation; Note=Translation N-terminally shortened;
Secondary accessions: B7Z3E6 F5H773 Q9HDA4
Alternative splicing: 2 isoforms:  Q9ULL4-1   Q9ULL4-2   

Explore the universe of human proteins at neXtProt for PLXNB3: NX_Q9ULL4

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q9ULL4

  • PLXNB3 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (2 alternative transcripts): 
    NP_001156729.1  NP_005384.2  

    ENSEMBL proteins: 
     ENSP00000355378   ENSP00000391650   ENSP00000396048   ENSP00000412454   ENSP00000445569  
     ENSP00000441919   ENSP00000444086   ENSP00000442736  
    Reactome Protein details: Q9ULL4
    Human Recombinant Protein Products: 
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    Uscn Proteins for PLXNB3

    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--


    PLXNB3 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

    PLXNB3 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 Q9ULL4

    ProtoNet protein and cluster: Q9ULL4

    1 Blocks protein family: IPB013548 Plexin cytoplasmic region

    UniProtKB/Swiss-Prot: PLXB3_HUMAN, Q9ULL4
    Similarity: Belongs to the plexin family
    Similarity: Contains 4 IPT/TIG domains
    Similarity: Contains 3 PSI domains
    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: PLXB3_HUMAN, Q9ULL4
    Function: Receptor for SEMA5A that plays a role in axon guidance, invasive growth and cell migration. Stimulates
    neurite outgrowth and mediates Ca(2+)/Mg(2+)-dependent cell aggregation. In glioma cells, SEMA5A stimulation of PLXNB3
    results in the disassembly of F-actin stress fibers, disruption of focal adhesions and cellular collapse as well as
    inhibition of cell migration and invasion through ARHGDIA-mediated inactivation of RAC1

         Genatlas biochemistry entry for PLXNB3:
    plexin B3,calcium-dependent cell adhesion molecule at the neuronal cell surface

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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:0005096GTPase activator activity ----
    GO:0005515protein binding IPI--


    PLXNB3 for ontologies           About GeneDecksing


    Animal Models:
         Mouse knock-out Plxnb3tm1Mom for PLXNB3
         1 MGI mutant phenotype (inferred from 1 allele(MGI details for Plxnb3):
     vision/eye 

    PLXNB3 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 PLXNB3
        Developmental Biology
    Semaphorin interactions
    Other semaphorin interactions
    Axon guidance


    1         Kegg Pathway  (Kegg details for PLXNB3):
        Axon guidance


    PLXNB3 for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for PLXNB3

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/27 Interacting proteins for PLXNB3 (Q9ULL41, 2, 3 ENSP000003553784) via UniProtKB, MINT, STRING, and/or I2D (see all 27)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    METP085811, 3, ENSP000003172724EBI-311073,EBI-1039152 I2D: score=1 STRING: ENSP00000317272
    MST1RQ049121, 3, ENSP000002964744EBI-311073,EBI-2637518 I2D: score=1 STRING: ENSP00000296474
    SEMA4AQ9H3S12, 3, ENSP000003471174MINT-4507872 I2D: score=1 STRING: ENSP00000347117
    ARHGEF11O150853, ENSP000003571774I2D: score=3 STRING: ENSP00000357177
    MAGI2Q86UL83, ENSP000003461514I2D: score=2 STRING: ENSP00000346151
    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:0007165signal transduction IEA--
    GO:0007275multicellular organismal development ----
    GO:0007411axon guidance TAS--
    GO:0051056regulation of small GTPase mediated signal transduction ----


    PLXNB3 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 PLXNB3
    Search CenterWatch for drugs/clinical trials and news about PLXNB3 / PLXB3 

    (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 PLXNB3 gene (2 alternative transcripts): 
    NM_001163257.1  NM_005393.2  

    Unigene Cluster for PLXNB3:

    Plexin B3
    Hs.632833  [show with all ESTs]
    Unigene Representative Sequence: NM_001163257
    12 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000361971 ENST00000411613 ENST00000482654 ENST00000455214 ENST00000485980
    ENST00000448847 ENST00000469190 ENST00000472415 ENST00000538776(uc004fij.1)
    ENST00000538282 ENST00000538543 ENST00000538966(uc011mzb.1 uc011mzc.2 uc010nuk.2 uc004fii.2 uc011mzd.1)


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    Additional cDNA sequence: 

    AB033032.1 AF149019.1 AK292535.1 AK295762.1 AK295849.1 AK295894.1 AK296538.1 AK304705.1 
    AK307894.1 AY927551.1 BC131771.1 

    11 DOTS entries:

    DT.411749  DT.121309495  DT.102822682  DT.40109611  DT.100740225  DT.121309427  DT.121309449  DT.121309420 
    DT.121309478  DT.91992878  DT.92421832 

    24/64 AceView cDNA sequences (see all 64):

    CD517568 Z40628 BQ722416 BF345653 NM_005393 BP348957 R46653 AF149019 
    CA397317 AB033032 BF528615 AL039923 BE890324 AI609808 BG912057 CA313922 
    BM721178 CA425482 CD300029 BG913187 BX091694 BM723513 BM688626 BM689380 

    GeneLoc Exon Structure

    5/15 Alternative Splicing Database (ASD) splice patterns (SP) for PLXNB3 (see all 15)    About this scheme

    ExUns: 1 ^ 2 ^ 3 ^ 4a · 4b ^ 5 ^ 6 ^ 7 ^ 8 ^ 9 ^ 10 ^ 11 ^ 12 ^ 13a · 13b ^ 14 ^ 15 ^ 16a · 16b · 16c ^ 17 ^ 18 ^ 19a · 19b ^ 20 ^ 21 ^
    SP1:        -                                                                                                           -                                       
    SP2:                                                                                                                                                            
    SP3:                                                                                                                                                            
    SP4:                                                                                                                                                            
    SP5:                                                                                                                                                            

    ExUns: 22 ^ 23 ^ 24a · 24b · 24c ^ 25 ^ 26a · 26b · 26c ^ 27 ^ 28a · 28b ^ 29a · 29b · 29c · 29d ^ 30 ^ 31a · 31b ^ 32a · 32b ^ 33 ^ 34 ^ 35a · 35b · 35c ·
    SP1:                                                                                                              -                             -     -         
    SP2:                                                                          -     -     -     -                                                               
    SP3:                                      -                                                                                                                     
    SP4:                                                                                      -     -                 -                                             
    SP5:                                                                                                                                                            

    ExUns: 35d ^ 36 ^ 37 ^ 38a · 38b · 38c
    SP1:                                    
    SP2:                                    
    SP3:                                    
    SP4:                                    
    SP5:                    -               


    ECgene alternative splicing isoforms for PLXNB3

    (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

    PLXNB3 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: AAGGGCACGC

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

    About this image
    See PLXNB3 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for PLXNB3

    SOURCE GeneReport for Unigene cluster: Hs.632833

    UniProtKB/Swiss-Prot: PLXB3_HUMAN, Q9ULL4
    Tissue specificity: Expression detected in Purkinje and granular cells in cerebellum, and in brain neocortex but not in
    corpus callosum. Expressed in glioma cells and embryonic kidney cells (at protein level). Expressed in brain, liver,
    pancreas and placenta, with weak expression detected also in lung and kidney. Expressed in several glioma cell lines

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    In Situ
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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 PLXNB3 gene from 5/18 species (see all 18)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    lizard
    (Anolis carolinensis)
    Reptilia PLXNB36
    --
    55(a)
    1 ↔ 1
    2(86565621-86662335)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.57272 Xenopus laevis transcribed sequence with weak similarity more 74.86(n)    BX848740.1 
    zebrafish
    (Danio rerio)
    Actinopterygii plxnb31 plexin B3 59.12(n)
    55.01(a)
      566546  XM_689822.5  XP_694914.3 
    fruit fly
    (Drosophila melanogaster)
    Insecta plexB3 axon guidance semaphorin receptor 40(a)   102A1   --
    worm
    (Caenorhabditis elegans)
    Secernentea plx-23   -- 25(a)   II(14413677-14421269)   --


    ENSEMBL Gene Tree for PLXNB3 (if available)
    TreeFam Gene Tree for PLXNB3 (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for PLXNB3 gene
    PLXNB22  PLXND12  PLXNA32  PLXNA12  PLXNA22  PLXNB12  PLXNC12  PLXNA42  
    11 SIMAP similar genes for PLXNB3 using alignment to 7 protein entries:     PLXB3_HUMAN (see all proteins):
    DKFZp761P19121    PLXNB1    PLXNB2    PLXND1    Nbla00445    MM1
    PLXNA2    PLXNC1    PLXNA1    PLXNA3    PLXNA4

    PLXNB3 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

    10/408 NCBI SNPs in PLXNB3 are shown (see all 408    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr X posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs59871511,2
    C,--141685299(+) GGACAC/TGTGTG 2 -- us2k10--------
    rs22837511,2
    C,F,H,--141686030(+) CCTCCC/TCAGAG 2 -- us2k14Minor allele frequency- T:0.08NS EA 418
    rs59869291,2
    C,--141686334(+) GCCCAG/ACGCCT 2 -- us2k12Minor allele frequency- A:0.00CSA 2
    rs7295721,2
    C,A,--141686734(-) CAATCA/GTGCCC 2 -- ut510--------
    rs70592591,2
    C,A,--141686849(+) GGCTTG/AGGCTT 2 -- int12Minor allele frequency- A:0.00NA 4
    rs78887521,2
    C,--141687028(+) GAACCA/TTGTTT 2 -- int10--------
    rs1846953641,2
    C,--141687411(+) CCCGTA/GGTCCT 2 -- int10--------
    rs59871521,2
    C,F,H,--141687998(+) CAATGC/TCCCCC 2 -- ut515Minor allele frequency- T:0.08NS NA CSA 506
    rs284420451,2
    C,--141688312(+) TGCTCC/TGCCCT 2 -- int13Minor allele frequency- T:0.00WA CSA 4
    rs120089291,2
    C,F,H--141688407(+) AAGGGG/TCTGCT 2 -- int1 trp31Minor allele frequency- T:0.50NA 4

    HapMap Linkage Disequilibrium report for PLXNB3 (153029651 - 153044801 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for PLXNB3
         1 CNV: 97103
    Locus Specific Mutation Databases (LSDB): PLXNB3

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    (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

    PLXNB3 for disorders           About GeneDecksing

    OMIM gene information: 300214    OMIM disorders: --

    5 diseases for PLXNB3:    About MalaCards
    sporadic breast cancer    breast cancer    leukemia    neuronitis
    carcinoma


    Export disorders for PLXNB3 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 PLXNB3 gene, integrated from 9 sources (see all 22):
    (articles sorted by number of sources associating them with PLXNB3)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Plexin-B3 is a functional receptor for semaphorin 5A. (PubMed id 15218527)1, 2, 9 Artigiani S.... Tamagnone L. (2004)
    2. Plexin B3 promotes neurite outgrowth, interacts homophilically, and interacts with Rin. (PubMed id 16122393)1, 2, 9 Hartwig C....Finckh U. (2005)
    3. Semaphorin 5A and plexin-B3 regulate human glioma cell motility and morphology through Rac1 and the actin cytoskeleton. (PubMed id 21706053)1, 2 Li X....Lee A.Y. (2012)
    4. Semaphorin 5A and plexin-B3 inhibit human glioma cell motility through RhoGDIalpha-mediated inactivation of Rac1 GTPase. (PubMed id 20696765)1, 2 Li X. and Lee A.Y. (2010)
    5. Interplay between scatter factor receptors and B plexins controls invasive growth. (PubMed id 15184888)1, 2 Conrotto P.... Giordano S. (2004)
    6. Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (PubMed id 10574462)1, 2 Nagase T.... Ohara O. (1999)
    7. Plexins are a large family of receptors for transmembrane, secreted and GPI-anchored semaphorins in vertebrates. (PubMed id 10520995)1, 3 Tamagnone L.... Comoglio P.M. (1999)
    8. Plexin B3 is genetically associated with verbal performance and white matter volume in human brain. (PubMed id 17033634)1, 9 Rujescu D....Finckh U. (2007)
    9. Identification of semaphorin 5A interacting protein by applying apriori knowledge and peptide complementarity related to protein evolution and structure. (PubMed id 19329067)1, 9 Sadanandam A....Singh R.K. (2008)
    10. The DNA sequence of the human X chromosome. (PubMed id 15772651)2 Ross M.T.... Bentley D.R. (2005)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    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: 5365 HGNC: 9105 AceView: PLXNB3 Ensembl:ENSG00000198753 euGenes: HUgn5365
    ECgene: PLXNB3 Kegg: 5365 H-InvDB: PLXNB3

    (According to HUGE)
    About This Section
    HUGE: KIAA1206

    (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 PLXNB3 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 PLXNB3 gene:
    Search GeneIP for patents involving PLXNB3

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



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