Gene Gene information from NCBI Gene database.
Entrez ID 8828
Gene name Neuropilin 2
Gene symbol NRP2
Synonyms (NCBI Gene)
NP2NPN2PRO2714VEGF165R2
Chromosome 2
Chromosome location 2q33.3
Summary 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, i
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs779617179 T>- Likely-pathogenic Frameshift variant, coding sequence variant, intron variant, genic downstream transcript variant
miRNA miRNA information provided by mirtarbase database.
133
miRTarBase ID miRNA Experiments Reference
MIRT017537 hsa-miR-335-5p Microarray 18185580
MIRT019236 hsa-miR-331-3p Sequencing 20371350
MIRT025587 hsa-miR-10b-5p Reporter assay 21642433
MIRT019236 hsa-miR-331-3p Luciferase reporter assayWestern blot 24142150
MIRT437981 hsa-miR-196a-5p Luciferase reporter assay 24681820
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
73
GO ID Ontology Definition Evidence Reference
GO:0001525 Process Angiogenesis IEA
GO:0001525 Process Angiogenesis NAS 11112349
GO:0001764 Process Neuron migration IEA
GO:0001938 Process Positive regulation of endothelial cell proliferation IEA
GO:0001938 Process Positive regulation of endothelial cell proliferation TAS 21245381
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602070 8005 ENSG00000118257
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O60462
Protein name Neuropilin-2 (Vascular endothelial cell growth factor 165 receptor 2)
Protein function High affinity receptor for semaphorins 3C, 3F, VEGF-165 and VEGF-145 isoforms of VEGF, and the PLGF-2 isoform of PGF.; (Microbial infection) Acts as a receptor for human cytomegalovirus pentamer-dependent entry in epithelial and endoth
PDB 2QQJ , 2QQK , 2QQL , 2QQO , 4QDQ , 4QDR , 4QDS , 5DN2 , 5DQ0 , 6GH8 , 6TDB , 6TJT , 7M22 , 7T4S , 8IVW , 8IVX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00431 CUB 28 139 CUB domain Domain
PF00431 CUB 149 264 CUB domain Domain
PF00754 F5_F8_type_C 292 424 F5/8 type C domain Domain
PF00754 F5_F8_type_C 449 589 F5/8 type C domain Domain
PF00629 MAM 646 801 MAM domain, meprin/A5/mu Domain
PF11980 DUF3481 850 931 C-terminal domain of neuropilin glycoprotein Family
Sequence
MDMFPLTWVFLALYFSRHQVRGQPDPPCGGRLNSKDAGYITSPGYPQDYPSHQNCEWIVY
APEPNQKIVLNFNPHFEIEKHDCKYDFIEIRDGDSESADLLGKHCGNIAPPTIISSGSML
YIKFTSDYARQGAGFSLRY
EIFKTGSEDCSKNFTSPNGTIESPGFPEKYPHNLDCTFTIL
AKPKMEIILQFLIFDLEHDPLQVGEGDCKYDWLDIWDGIPHVGPLIGKYCGTKTPSELRS
STGILSLTFHTDMAVAKDGFSARY
YLVHQEPLENFQCNVPLGMESGRIANEQISASSTYS
DGRWTPQQSRLHGDDNGWTPNLDSNKEYLQVDLRFLTMLTAIATQGAISRETQNGYYVKS
YKLEVSTNGEDWMVYRHGKNHKVFQANNDATEVVLNKLHAPLLTRFVRIRPQTWHSGIAL
RLEL
FGCRVTDAPCSNMLGMLSGLIADSQISASSTQEYLWSPSAARLVSSRSGWFPRIPQ
AQPGEEWLQVDLGTPKTVKGVIIQGARGGDSITAVEARAFVRKFKVSYSLNGKDWEYIQD
PRTQQPKLFEGNMHYDTPDIRRFDPIPAQYVRVYPERWSPAGIGMRLEV
LGCDWTDSKPT
VETLGPTVKSEETTTPYPTEEEATECGENCSFEDDKDLQLPSGFNCNFDFLEEPCGWMYD
HAKWLRTTWASSSSPNDRTFPDDRNFLRLQSDSQREGQYARLISPPVHLPRSPVCMEFQY
QATGGRGVALQVVREASQESKLLWVIREDQGGEWKHGRIILPSYDMEYQIVFEGVIGKGR
SGEIAIDDIRISTDVPLENCM
EPISAFAGENFKVDIPEIHEREGYEDEIDDEYEVDWSNS
SSATSGSGAPSTDKEKSWLYTLDPILITIIAMSSLGVLLGATCAGLLLYCTCSYSGLSSR
SCTTLENYNFELYDGLKHKVKMNHQKCCSEA
Sequence length 931
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Virion - Lassa virus and SFTS virus   Neurophilin interactions with VEGF and VEGFR
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
157
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
NRP2-related disorder Likely pathogenic rs779617179 RCV004748864
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Benign rs2228642 RCV005903464
Gastric cancer Benign rs2228642 RCV005903465
Hirschsprung disease, susceptibility to, 1 Uncertain significance rs114144673 RCV000508614
Ovarian serous cystadenocarcinoma Likely benign rs374822572 RCV005936899
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 39232098
Arteriovenous Malformations Associate 21921738
Asthma Associate 30206357
Breast Neoplasms Associate 17912247, 19580679, 23613720, 26673618, 33396906
Breast Neoplasms Stimulate 22302985
Carcinogenesis Associate 39232098
Carcinoma Adenoid Cystic Associate 28961428
Carcinoma Hepatocellular Associate 26573807, 37928273
Carcinoma Intraductal Noninfiltrating Associate 28062852
Carcinoma Non Small Cell Lung Associate 12412174, 12845630