NRP2
Neuropilin-2
Also known as: NRP2_HUMAN, VEGF165R2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O60462
- Gene
- NRP2
- Ensembl
- ENSG00000118257
- Chromosome
- 2
- Canonical length
- 931 aa
- Protein class
- Cancer-related genes, Plasma proteins, Predicted membrane proteins, Predicted secreted proteins, Transporters
- Subcellular location
- Nucleoplasm,Vesicles,Plasma membrane
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
This gene encodes a member of the neuropilin family of receptor proteins. The encoded transmembrane protein binds to SEMA3C protein {sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C} and SEMA3F protein {sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F}, and interacts with vascular endothelial growth factor (VEGF). This protein may play a role in cardiovascular development, axon guidance, and tumorigenesis. This protein has also been determined to act as a co-receptor for SARS-CoV-2 (which causes COVID-19) to infect host cells. [provided by RefSeq, Jul 2021]
Canonical amino-acid sequenceUniProt
931 residues, UniProt reviewed canonical sequence.
>O60462|NRP2
1 MDMFPLTWVF LALYFSRHQV RGQPDPPCGG RLNSKDAGYI TSPGYPQDYP SHQNCEWIVY
61 APEPNQKIVL NFNPHFEIEK HDCKYDFIEI RDGDSESADL LGKHCGNIAP PTIISSGSML
121 YIKFTSDYAR QGAGFSLRYE IFKTGSEDCS KNFTSPNGTI ESPGFPEKYP HNLDCTFTIL
181 AKPKMEIILQ FLIFDLEHDP LQVGEGDCKY DWLDIWDGIP HVGPLIGKYC GTKTPSELRS
241 STGILSLTFH TDMAVAKDGF SARYYLVHQE PLENFQCNVP LGMESGRIAN EQISASSTYS
301 DGRWTPQQSR LHGDDNGWTP NLDSNKEYLQ VDLRFLTMLT AIATQGAISR ETQNGYYVKS
361 YKLEVSTNGE DWMVYRHGKN HKVFQANNDA TEVVLNKLHA PLLTRFVRIR PQTWHSGIAL
421 RLELFGCRVT DAPCSNMLGM LSGLIADSQI SASSTQEYLW SPSAARLVSS RSGWFPRIPQ
481 AQPGEEWLQV DLGTPKTVKG VIIQGARGGD SITAVEARAF VRKFKVSYSL NGKDWEYIQD
541 PRTQQPKLFE GNMHYDTPDI RRFDPIPAQY VRVYPERWSP AGIGMRLEVL GCDWTDSKPT
601 VETLGPTVKS EETTTPYPTE EEATECGENC SFEDDKDLQL PSGFNCNFDF LEEPCGWMYD
661 HAKWLRTTWA SSSSPNDRTF PDDRNFLRLQ SDSQREGQYA RLISPPVHLP RSPVCMEFQY
721 QATGGRGVAL QVVREASQES KLLWVIREDQ GGEWKHGRII LPSYDMEYQI VFEGVIGKGR
781 SGEIAIDDIR ISTDVPLENC MEPISAFAGE NFKVDIPEIH EREGYEDEID DEYEVDWSNS
841 SSATSGSGAP STDKEKSWLY TLDPILITII AMSSLGVLLG ATCAGLLLYC TCSYSGLSSR
901 SCTTLENYNF ELYDGLKHKV KMNHQKCCSE ALocalizationUniProt · AlphaFold · HPA
Whether an antibody against NRP2 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 74 nTPM
Expression across tissuesHPA
Tissue
- colon: 74 nTPM
- ovary: 51 nTPM
- smooth muscle: 51 nTPM
- placenta: 44 nTPM
- endometrium: 43 nTPM
- urinary bladder: 40 nTPM
Single-cell type
- lymphatic endothelial cells: 428 nCPM
- hofbauer cells: 378 nCPM
- smooth muscle cells: 216 nCPM
- macrophages: 211 nCPM
- transitional alveolar cells: 184 nCPM
- epididymal basal cells: 153 nCPM
Immune cell
- classical monocyte: 0.3 nTPM
- naive B-cell: 0.2 nTPM
- total PBMC: 0.1 nTPM
- basophil: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- hypothalamus: 92 nTPM
- medulla oblongata: 66 nTPM
- midbrain: 52 nTPM
- thalamus: 50 nTPM
- hippocampal formation: 46 nTPM
- pons: 42 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about NRP2.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 397 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Inborn genetic diseases
- NRP2-related disorder
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)
- 0.48
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.18
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
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
- angiogenesis
- axon extension involved in axon guidance
- axon guidance
- branchiomotor neuron axon guidance
- cell adhesion
- cellular response to leukemia inhibitory factor
- dorsal root ganglion morphogenesis
- facial nerve structural organization
- facioacoustic ganglion development
- gonadotrophin-releasing hormone neuronal migration to the hypothalamus
- negative chemotaxis
- nerve development
- neural crest cell migration involved in autonomic nervous system development
- outflow tract septum morphogenesis
- positive regulation of endothelial cell migration
- positive regulation of endothelial cell proliferation
- regulation of postsynapse organization
- semaphorin-plexin signaling pathway
- sensory neuron axon guidance
- sympathetic ganglion development
- sympathetic neuron projection extension
- sympathetic neuron projection guidance
- trigeminal ganglion development
- trigeminal nerve structural organization
- ventral trunk neural crest cell migration
- vestibulocochlear nerve structural organization
Molecular functions
- cytokine binding
- growth factor binding
- heparin binding
- identical protein binding
- metal ion binding
- semaphorin receptor activity
- signaling receptor activity
- vascular endothelial growth factor receptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Coagulation factor 5/8, C-terminal domain
- CUB domain
- MAM domain
- Galactose-binding-like domain superfamily
- Concanavalin A-like lectin/glucanase domain superfamily
- Neuropilin
- Neuropilin, C-terminal
- Spermadhesin, CUB domain superfamily
- Neuropilin/Multicopper Oxidase/Coagulation Factor
- CUB domain
- MAM domain, meprin/A5/mu
- F5/8 type C domain
- C-terminal domain of neuropilin glycoprotein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NRP2 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 NRP2 as an antibody target. Whether an autoantibody or antibody against NRP2 could matter depends on whether native NRP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NRP2 is annotated as secreted, so native NRP2 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label NRP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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