Human Gene PLXNB3 (ENST00000538966.5) from GENCODE V44
  Description: Homo sapiens plexin B3 (PLXNB3), transcript variant 2, mRNA. (from RefSeq NM_001163257)
RefSeq Summary (NM_001163257): 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].
Gencode Transcript: ENST00000538966.5
Gencode Gene: ENSG00000198753.12
Transcript (Including UTRs)
   Position: hg38 chrX:153,764,196-153,779,346 Size: 15,151 Total Exon Count: 37 Strand: +
Coding Region
   Position: hg38 chrX:153,766,211-153,779,039 Size: 12,829 Coding Exon Count: 35 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesMethods
Data last updated at UCSC: 2023-08-18 00:09:47

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chrX:153,764,196-153,779,346)mRNA (may differ from genome)Protein (1932 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
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HGNCLynxMalacardsMGImyGene2neXtProt
OMIMPubMedReactomeUniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: PLXB3_HUMAN
DESCRIPTION: RecName: Full=Plexin-B3; Flags: Precursor;
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.
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).
INTERACTION: P08581:MET; NbExp=2; IntAct=EBI-311073, EBI-1039152; Q04912:MST1R; NbExp=2; IntAct=EBI-311073, EBI-2637518;
SUBCELLULAR LOCATION: Cell membrane; Single-pass type I membrane protein. Note=Colocalizes with RIT2/RIN at the plasma membrane.
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.
SIMILARITY: Belongs to the plexin family.
SIMILARITY: Contains 4 IPT/TIG domains.
SIMILARITY: Contains 3 PSI domains.
SIMILARITY: Contains 1 Sema domain.
SEQUENCE CAUTION: Sequence=BAA86520.1; Type=Erroneous initiation; Note=Translation N-terminally shortened;

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: PLXNB3
Diseases sorted by gene-association score: glioma (5)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 37.88 RPKM in Nerve - Tibial
Total median expression: 433.62 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -105.80271-0.390 Picture PostScript Text
3' UTR -93.20307-0.304 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR013783 - Ig-like_fold
IPR014756 - Ig_E-set
IPR002909 - IPT_TIG_rcpt
IPR003659 - Plexin-like
IPR016201 - Plexin-like_fold
IPR013548 - Plexin_cytoplasmic_RasGAP_dom
IPR002165 - Plexin_repeat
IPR008936 - Rho_GTPase_activation_prot
IPR001627 - Semaphorin/CD100_Ag
IPR015943 - WD40/YVTN_repeat-like_dom

Pfam Domains:
PF08337 - Plexin cytoplasmic RasGAP domain
PF01437 - Plexin repeat
PF01403 - Sema domain
PF01833 - IPT/TIG domain

ModBase Predicted Comparative 3D Structure on Q9ULL4
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-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
Genome BrowserGenome BrowserNo orthologNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
MGIRGD    
Protein SequenceProtein Sequence    
AlignmentAlignment    

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0005515 protein binding
GO:0017154 semaphorin receptor activity
GO:0019904 protein domain specific binding
GO:0051022 Rho GDP-dissociation inhibitor binding
GO:0098632 protein binding involved in cell-cell adhesion

Biological Process:
GO:0001938 positive regulation of endothelial cell proliferation
GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules
GO:0007162 negative regulation of cell adhesion
GO:0007165 signal transduction
GO:0007399 nervous system development
GO:0008360 regulation of cell shape
GO:0010593 negative regulation of lamellipodium assembly
GO:0010976 positive regulation of neuron projection development
GO:0030336 negative regulation of cell migration
GO:0034260 negative regulation of GTPase activity
GO:0048675 axon extension
GO:0050772 positive regulation of axonogenesis
GO:0050918 positive chemotaxis
GO:0060326 cell chemotaxis
GO:0071526 semaphorin-plexin signaling pathway

Cellular Component:
GO:0005886 plasma membrane
GO:0009986 cell surface
GO:0016020 membrane
GO:0016021 integral component of membrane


-  Descriptions from all associated GenBank mRNAs
  AK292535 - Homo sapiens cDNA FLJ76953 complete cds, highly similar to Homo sapiens plexin B3 (PLXNB3), mRNA.
AK307894 - Homo sapiens cDNA, FLJ97842.
AB033032 - Homo sapiens KIAA1206 mRNA for KIAA1206 protein.
AF149019 - Homo sapiens plexin-B3 (PLXNB3) mRNA, complete cds.
AK296538 - Homo sapiens cDNA FLJ59918 complete cds, highly similar to Plexin-B3 precursor.
AK295894 - Homo sapiens cDNA FLJ50412 complete cds, highly similar to Plexin-B3 precursor.
AK304705 - Homo sapiens cDNA FLJ61676 complete cds, highly similar to Plexin-B3 precursor.
JD506588 - Sequence 487612 from Patent EP1572962.
AK295849 - Homo sapiens cDNA FLJ50544 complete cds, highly similar to Plexin-B3 precursor.
AK295762 - Homo sapiens cDNA FLJ59541 complete cds, highly similar to Plexin-B3 precursor.
JD483278 - Sequence 464302 from Patent EP1572962.
AB384140 - Synthetic construct DNA, clone: pF1KSDA1206, Homo sapiens PLXNB3 gene for plexin-B3 precursor, complete cds, without stop codon, in Flexi system.
BC172435 - Synthetic construct Homo sapiens clone IMAGE:100069129, MGC:199140 plexin B3 (PLXNB3) mRNA, encodes complete protein.
AY927551 - Homo sapiens mRNA sequence.
AB209155 - Homo sapiens mRNA for serine/threonine kinase 23 variant protein.
JD538935 - Sequence 519959 from Patent EP1572962.
JD389976 - Sequence 371000 from Patent EP1572962.
JD169923 - Sequence 150947 from Patent EP1572962.
JD310415 - Sequence 291439 from Patent EP1572962.
JD189519 - Sequence 170543 from Patent EP1572962.
JD121958 - Sequence 102982 from Patent EP1572962.
JD100046 - Sequence 81070 from Patent EP1572962.
JD253329 - Sequence 234353 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa04360 - Axon guidance

Reactome (by CSHL, EBI, and GO)

Protein Q9ULL4 (Reactome details) participates in the following event(s):

R-HSA-416698 SEMA5A binds to PLXNB3
R-HSA-416700 Other semaphorin interactions
R-HSA-373755 Semaphorin interactions
R-HSA-422475 Axon guidance
R-HSA-1266738 Developmental Biology

-  Other Names for This Gene
  Alternate Gene Symbols: B7Z3E6, ENST00000538966.1, ENST00000538966.2, ENST00000538966.3, ENST00000538966.4, F5H773, KIAA1206, NM_001163257, PLXB3_HUMAN, PLXN6, Q9HDA4, Q9ULL4, uc010nuk.1, uc010nuk.2, uc010nuk.3
UCSC ID: ENST00000538966.5
RefSeq Accession: NM_001163257
Protein: Q9ULL4 (aka PLXB3_HUMAN or PXB3_HUMAN)
CCDS: CCDS55536.1, CCDS14729.1

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.