Gene Gene information from NCBI Gene database.
Entrez ID 5364
Gene name Plexin B1
Gene symbol PLXNB1
Synonyms (NCBI Gene)
PLEXIN-B1PLXN5SEP
Chromosome 3
Chromosome location 3p21.31
miRNA miRNA information provided by mirtarbase database.
35
miRTarBase ID miRNA Experiments Reference
MIRT005765 hsa-miR-214-3p GFP reporter assayImmunohistochemistryqRT-PCRWestern blot 21216304
MIRT005765 hsa-miR-214-3p GFP reporter assayImmunohistochemistryqRT-PCRWestern blot 21216304
MIRT005765 hsa-miR-214-3p Microarray;Other 19859982
MIRT1243801 hsa-miR-1193 CLIP-seq
MIRT1243802 hsa-miR-1265 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
55
GO ID Ontology Definition Evidence Reference
GO:0002116 Component Semaphorin receptor complex IBA
GO:0002116 Component Semaphorin receptor complex IDA 19843518
GO:0002116 Component Semaphorin receptor complex IEA
GO:0002116 Component Semaphorin receptor complex ISS
GO:0002116 Component Semaphorin receptor complex TAS 19909241
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601053 9103 ENSG00000164050
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O43157
Protein name Plexin-B1 (Semaphorin receptor SEP)
Protein function Receptor for SEMA4D (PubMed:19843518, PubMed:20877282, PubMed:21912513). Plays a role in GABAergic synapse development (By similarity). Mediates SEMA4A- and SEMA4D-dependent inhibitory synapse development (By similarity). Plays a role in RHOA ac
PDB 2JPH , 2OS6 , 2R2O , 2REX , 3HM6 , 3OL2 , 3SU8 , 3SUA , 5B4W , 7VF3 , 7VG7 , 8B3K
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01403 Sema 37 460 Sema domain Family
PF01437 PSI 481 534 Plexin repeat Family
PF17960 TIG_plexin 540 627 TIG domain Domain
PF18020 TIG_2 921 1020 TIG domain found in plexin Domain
PF01833 TIG 1070 1159 IPT/TIG domain Domain
PF01833 TIG 1162 1248 IPT/TIG domain Domain
PF01833 TIG 1252 1374 IPT/TIG domain Domain
PF08337 Plexin_cytopl 1562 2102 Plexin cytoplasmic RasGAP domain Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in fetal kidney, and at slightly lower levels in fetal brain, lung and liver. {ECO:0000269|PubMed:8570614}.
Sequence
MPALGPALLQALWAGWVLTLQPLPPTAFTPNGTYLQHLARDPTSGTLYLGATNFLFQLSP
GLQLEATVSTGPVLDSRDCLPPVMPDECPQAQPTNNPNQLLLVSPGALVVCGSVHQGVCE
QRRLGQLEQLLLRPERPGDTQYVAANDPAVSTVGLVAQGLAGEPLLFVGRGYTSRGVGGG
IPPITTRALWPPDPQAAFSYEETAKLAVGRLSEYSHHFVSAFARGASAYFLFLRRDLQAQ
SRAFRAYVSRVCLRDQHYYSYVELPLACEGGRYGLIQAAAVATSREVAHGEVLFAAFSSA
APPTVGRPPSAAAGASGASALCAFPLDEVDRLANRTRDACYTREGRAEDGTEVAYIEYDV
NSDCAQLPVDTLDAYPCGSDHTPSPMASRVPLEATPILEWPGIQLTAVAVTMEDGHTIAF
LGDSQGQLHRVYLGPGSDGHPYSTQSIQQGSAVSRDLTFD
GTFEHLYVMTQSTLLKVPVA
SCAQHLDCASCLAHRDPYCGWCVLLGRCSRRSECSRGQGPEQWLWSFQPELGCLQVAAMS
PANISREETREVFLSVPDLPPLWPGESYSCHFGEHQSPALLTGSGVMCPSPDPSEAPVLP
RGADYVSVSVELRFGAVVIAKTSLSFY
DCVAVTELRPSAQCQACVSSRWGCNWCVWQHLC
THKASCDAGPMVASHQSPLVSPDPPARGGPSPSPPTAPKALATPAPDTLPVEPGAPSTAT
ASDISPGASPSLLSPWGPWAGSGSISSPGSTGSPLHEEPSPPSPQNGPGTAVPAPTDFRP
SATPEDLLASPLSPSEVAAVPPADPGPEALHPTVPLDLPPATVPATTFPGAMGSVKPALD
WLTREGGELPEADEWTGGDAPAFSTSTLLSGDGDSAELEGPPAPLILPSSLDYQYDTPGL
WELEEATLGASSCPCVESVQGSTLMPVHVEREIRLLGRNLHLFQDGPGDNECVMELEGLE
VVVEARVECEPPPDTQCHVTCQQHQLSYEALQPELRVGLFLRRAGRLRVDSAEGLHVVLY

DCSVGHGDCSRCQTAMPQYGCVWCEGERPRCVTREACGEAEAVATQCPAPLIHSVEPLTG
PVDGGTRVTIRGSNLGQHVQDVLGMVTVAGVPCAVDAQEYEVSSSLVCITGASGEEVAGA
TAVEVPGRGRGVSEHDFAY
QDPKVHSIFPARGPRAGGTRLTLNGSKLLTGRLEDIRVVVG
DQPCHLLPEQQSEQLRCETSPRPTPATLPVAVWFGATERRLQRGQFKY
TLDPNITSAGPT
KSFLSGGREICVRGQNLDVVQTPRIRVTVVSRMLQPSQGLGRRRRVVPETACSLGPSCSS
QQFEEPCHVNSSQLITCRTPALPGLPEDPWVRVEFILDNLVFDFATLNPTPFSY
EADPTL
QPLNPEDPTMPFRHKPGSVFSVEGENLDLAMSKEEVVAMIGDGPCVVKTLTRHHLYCEPP
VEQPLPRHHALREAPDSLPEFTVQMGNLRFSLGHVQYDGESPGAFPVAAQVGLGVGTSLL
ALGVIIIVLMYRRKSKQALRDYKKVQIQLENLESSVRDRCKKEFTDLMTEMTDLTSDLLG
SGIPFLDYKVYAERIFFPGHRESPLHRDLGVPESRRPTVEQGLGQLSNLLNSKLFLTKFI
HTLESQRTFSARDRAYVASLLTVALHGKLEYFTDILRTLLSDLVAQYVAKNPKLMLRRTE
TVVEKLLTNWMSICLYTFVRDSVGEPLYMLFRGIKHQVDKGPVDSVTGKAKYTLNDNRLL
REDVEYRPLTLNALLAVGPGAGEAQGVPVKVLDCDTISQAKEKMLDQLYKGVPLTQRPDP
RTLDVEWRSGVAGHLILSDEDVTSEVQGLWRRLNTLQHYKVPDGATVALVPCLTKHVLRE
NQDYVPGERTPMLEDVDEGGIRPWHLVKPSDEPEPPRPRRGSLRGGERERAKAIPEIYLT
RLLSMKGTLQKFVDDLFQVILSTSRPVPLAVKYFFDLLDEQAQQHGISDQDTIHIWKTNS
LPLRFWINIIKNPQFVFDVQTSDNMDAVLLVIAQTFMDACTLADHKLGRDSPINKLLYAR
DIPRYKRMVERYYADIRQTVPASDQEMNSVLAELSWNYSGDLGARVALHELYKYINKYYD
QI
ITALEEDGTAQKMQLGYRLQQIAAAVENKVTDL
Sequence length 2135
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Axon guidance   G alpha (12/13) signalling events
Sema4D mediated inhibition of cell attachment and migration
Sema4D induced cell migration and growth-cone collapse
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
57
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
EBV-positive nodal T- and NK-cell lymphoma Likely benign rs767726203 RCV004557894
Gastric cancer Benign rs141235519 RCV005907392
Hepatocellular carcinoma Benign rs61729215 RCV005913356
PLXNB1-related disorder Uncertain significance; Conflicting classifications of pathogenicity; Benign; Likely benign rs2038207611, rs571547770, rs1479550150, rs764270397, rs963461084, rs188697214, rs2529720342, rs35741089, rs146977900, rs61729217, rs984282538, rs61729213, rs112016313, rs377100211, rs200565688
View all (35 more)
RCV003397694
RCV003417029
RCV003405940
RCV003421186
RCV003400038
RCV003422497
RCV003397787
RCV003907030
RCV003921416
RCV003907305
RCV003924138
RCV003917289
RCV003931892
RCV003981707
RCV003974147
RCV003964517
RCV003974243
RCV003974271
RCV003897396
RCV003967321
RCV003944549
RCV003961607
RCV003919471
RCV003924546
RCV003924582
RCV003951688
RCV003931406
RCV003937010
RCV003956962
RCV003957049
RCV003944784
RCV003922086
RCV003932141
RCV003934199
RCV003959446
RCV003972310
RCV003969225
RCV004731591
RCV003903163
RCV003970702
RCV003970703
RCV003933243
RCV003905915
RCV003905916
RCV003970854
RCV003953336
RCV003920614
RCV003930620
RCV003920597
RCV003940500
RCV003940775
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 29908079
Aortic Aneurysm Thoracic Associate 31035427
Breast Neoplasms Associate 18275816
Carcinoma Hepatocellular Associate 17511039
Carcinoma Pancreatic Ductal Associate 21812859
Cognition Disorders Associate 29908079
Colitis Ulcerative Stimulate 39596507
Colorectal Neoplasms Associate 27456345
Coronary Artery Disease Associate 33381571
Head and Neck Neoplasms Associate 24114199