PLXNC1
Plexin-C1
Also known as: CD232, PLXC1_HUMAN, VESPR
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O60486
- Gene
- PLXNC1
- Ensembl
- ENSG00000136040
- Chromosome
- 12
- Canonical length
- 1568 aa
- Protein class
- CD markers, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Mitochondria
- Quaternary structure
- Homodimer
OverviewNCBI Gene
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]
Canonical amino-acid sequenceUniProt
1568 residues, UniProt reviewed canonical sequence.
>O60486|PLXNC1
1 MEVSRRKAPP RPPRPAAPLP LLAYLLALAA PGRGADEPVW RSEQAIGAIA ASQEDGVFVA
61 SGSCLDQLDY SLEHSLSRLY RDQAGNCTEP VSLAPPARPR PGSSFSKLLL PYREGAAGLG
121 GLLLTGWTFD RGACEVRPLG NLSRNSLRNG TEVVSCHPQG STAGVVYRAG RNNRWYLAVA
181 ATYVLPEPET ASRCNPAASD HDTAIALKDT EGRSLATQEL GRLKLCEGAG SLHFVDAFLW
241 NGSIYFPYYP YNYTSGAATG WPSMARIAQS TEVLFQGQAS LDCGHGHPDG RRLLLSSSLV
301 EALDVWAGVF SAAAGEGQER RSPTTTALCL FRMSEIQARA KRVSWDFKTA ESHCKEGDQP
361 ERVQPIASST LIHSDLTSVY GTVVMNRTVL FLGTGDGQLL KVILGENLTS NCPEVIYEIK
421 EETPVFYKLV PDPVKNIYIY LTAGKEVRRI RVANCNKHKS CSECLTATDP HCGWCHSLQR
481 CTFQGDCVHS ENLENWLDIS SGAKKCPKIQ IIRSSKEKTT VTMVGSFSPR HSKCMVKNVD
541 SSRELCQNKS QPNRTCTCSI PTRATYKDVS VVNVMFSFGS WNLSDRFNFT NCSSLKECPA
601 CVETGCAWCK SARRCIHPFT ACDPSDYERN QEQCPVAVEK TSGGGRPKEN KGNRTNQALQ
661 VFYIKSIEPQ KVSTLGKSNV IVTGANFTRA SNITMILKGT STCDKDVIQV SHVLNDTHMK
721 FSLPSSRKEM KDVCIQFDGG NCSSVGSLSY IALPHCSLIF PATTWISGGQ NITMMGRNFD
781 VIDNLIISHE LKGNINVSEY CVATYCGFLA PSLKSSKVRT NVTVKLRVQD TYLDCGTLQY
841 REDPRFTGYR VESEVDTELE VKIQKENDNF NISKKDIEIT LFHGENGQLN CSFENITRNQ
901 DLTTILCKIK GIKTASTIAN SSKKVRVKLG NLELYVEQES VPSTWYFLIV LPVLLVIVIF
961 AAVGVTRHKS KELSRKQSQQ LELLESELRK EIRDGFAELQ MDKLDVVDSF GTVPFLDYKH
1021 FALRTFFPES GGFTHIFTED MHNRDANDKN ESLTALDALI CNKSFLVTVI HTLEKQKNFS
1081 VKDRCLFASF LTIALQTKLV YLTSILEVLT RDLMEQCSNM QPKLMLRRTE SVVEKLLTNW
1141 MSVCLSGFLR ETVGEPFYLL VTTLNQKINK GPVDVITCKA LYTLNEDWLL WQVPEFSTVA
1201 LNVVFEKIPE NESADVCRNI SVNVLDCDTI GQAKEKIFQA FLSKNGSPYG LQLNEIGLEL
1261 QMGTRQKELL DIDSSSVILE DGITKLNTIG HYEISNGSTI KVFKKIANFT SDVEYSDDHC
1321 HLILPDSEAF QDVQGKRHRG KHKFKVKEMY LTKLLSTKVA IHSVLEKLFR SIWSLPNSRA
1381 PFAIKYFFDF LDAQAENKKI TDPDVVHIWK TNSLPLRFWV NILKNPQFVF DIKKTPHIDG
1441 CLSVIAQAFM DAFSLTEQQL GKEAPTNKLL YAKDIPTYKE EVKSYYKAIR DLPPLSSSEM
1501 EEFLTQESKK HENEFNEEVA LTEIYKYIVK YFDEILNKLE RERGLEEAQK QLLHVKVLFD
1561 EKKKCKWMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PLXNC1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.3
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- appendix: 19 nTPM
- spleen: 19 nTPM
- bone marrow: 16 nTPM
- lymph node: 15 nTPM
- testis: 14 nTPM
- ovary: 14 nTPM
Single-cell type
- neutrophils: 3,898 nCPM
- melanocytes: 658 nCPM
- neutrophil progenitors: 552 nCPM
- monocytes: 380 nCPM
- sertoli cells: 237 nCPM
- megakaryocyte-erythroid progenitors: 235 nCPM
Immune cell
- neutrophil: 17 nTPM
- eosinophil: 15 nTPM
- non-classical monocyte: 8.7 nTPM
- intermediate monocyte: 6.1 nTPM
- classical monocyte: 3.6 nTPM
- myeloid DC: 2.9 nTPM
Brain region
- hypothalamus: 48 nTPM
- midbrain: 36 nTPM
- white matter: 28 nTPM
- cerebellum: 28 nTPM
- cerebral cortex: 25 nTPM
- basal ganglia: 24 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.27
- gnomAD pLI
- 1
- gnomAD missense Z
- 3.98
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell adhesion
- negative regulation of cell adhesion
- positive regulation of axonogenesis
- regulation of cell migration
- regulation of cell shape
- regulation of synapse pruning
- semaphorin-plexin signaling pathway
- synapse assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Sema domain
- Plexin repeat
- IPT domain
- Rho GTPase activation protein
- Plexin, cytoplasmic RasGAP domain
- Immunoglobulin-like fold
- WD40/YVTN repeat-like-containing domain superfamily
- PSI domain
- Plexin family
- Sema domain superfamily
- Plexin, cytoplasmic RhoGTPase-binding domain
- Plexin repeat
- IPT/TIG domain
- Plexin cytoplasmic RasGAP domain
- Plexin cytoplasmic RhoGTPase-binding domain
- Plexin-C1, Sema domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PLXNC1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PLXNC1 as an antibody target. Whether an autoantibody or antibody against PLXNC1 could matter depends on whether native PLXNC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PLXNC1 is annotated at the cell surface, where native PLXNC1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label PLXNC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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