Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8828
Gene name Gene Name - the full gene name approved by the HGNC.
Neuropilin 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NRP2
Synonyms (NCBI Gene) Gene synonyms aliases
NP2, NPN2, PRO2714, VEGF165R2
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q33.3
Summary Summary of gene provided in NCBI Entrez 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, i
SNPs SNP information provided by dbSNP.
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.
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 assay, Western blot 24142150
MIRT437981 hsa-miR-196a-5p Luciferase reporter assay 24681820
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001525 Process Angiogenesis NAS 11112349
GO:0001938 Process Positive regulation of endothelial cell proliferation TAS 21245381
GO:0002116 Component Semaphorin receptor complex NAS 19909241
GO:0003148 Process Outflow tract septum morphogenesis ISS
GO:0005021 Function Vascular endothelial growth factor-activated receptor activity NAS 11112349, 19909241
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602070 8005 ENSG00000118257
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Autism Autistic Disorder rs121964908, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699
View all (8 more)
17427189
Multiple congenital anomalies Multiple congenital anomalies rs1057517732
Seizure Complex partial seizures, Generalized seizures, Visual seizure, Tonic - clonic seizures, Single Seizure rs587784365, rs28939683, rs74315390, rs28939684, rs74315391, rs267607198, rs74315392, rs118192244, rs118192250, rs121917749, rs121917750, rs121917751, rs121917752, rs267606670, rs267607061
View all (179 more)
18657176
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Associations from Text Mining
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