NRP1 (neuropilin 1) - Rat Genome Database

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Gene: NRP1 (neuropilin 1) Homo sapiens
Analyze
Symbol: NRP1
Name: neuropilin 1
RGD ID: 733081
HGNC Page HGNC:8004
Description: Enables GTPase activator activity and vascular endothelial growth factor binding activity. Involved in several processes, including cell surface receptor signaling pathway; cellular response to hepatocyte growth factor stimulus; and positive regulation of cellular component biogenesis. Located in cytosol; focal adhesion; and plasma membrane. Implicated in lung non-small cell carcinoma and tetralogy of Fallot. Biomarker of Alzheimer's disease; COVID-19; hepatocellular carcinoma; and renal cell carcinoma.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: BDCA4; CD304; DKFZp686A03134; DKFZp781F1414; neuropilin; neuropilin-1; NP1; NRP; transmembrane receptor; vascular endothelial cell growth factor 165 receptor; VEGF165R
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
NCBI Annotation Information: Note: This gene has been reviewed for its involvement in coronavirus biology, and is involved in SARS-CoV-2 infection.
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381033,177,493 - 33,334,667 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1033,177,492 - 33,336,262 (-)EnsemblGRCh38hg38GRCh38
GRCh371033,466,421 - 33,623,595 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361033,506,432 - 33,663,839 (-)NCBINCBI36Build 36hg18NCBI36
Build 341033,506,432 - 33,663,476NCBI
Celera1033,231,763 - 33,389,179 (-)NCBICelera
Cytogenetic Map10p11.22NCBI
HuRef1033,186,444 - 33,343,500 (-)NCBIHuRef
CHM1_11033,468,091 - 33,625,451 (-)NCBICHM1_1
T2T-CHM13v2.01033,206,293 - 33,375,463 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-demecolcine  (EXP)
(1->4)-beta-D-glucan  (ISO)
1,1-dichloroethene  (ISO)
17alpha-ethynylestradiol  (EXP)
17beta-estradiol  (EXP,ISO)
17beta-estradiol 3-benzoate  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,4,6-tribromophenol  (EXP)
2-palmitoylglycerol  (EXP)
3,3',5,5'-tetrabromobisphenol A  (EXP)
3,3',5-triiodo-L-thyronine  (ISO)
3-chloropropane-1,2-diol  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
3-Nitrobenzanthrone  (EXP)
3H-1,2-dithiole-3-thione  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
4-hydroxynon-2-enal  (ISO)
4-hydroxyphenyl retinamide  (ISO)
5-aza-2'-deoxycytidine  (EXP)
5-fluorouracil  (EXP)
8-Br-cAMP  (EXP)
acetaldehyde  (ISO)
acetamide  (ISO)
acrylamide  (ISO)
aflatoxin B1  (EXP,ISO)
all-trans-retinoic acid  (EXP)
amitrole  (ISO)
ammonium chloride  (ISO)
amphetamine  (ISO)
antimycin A  (ISO)
aristolochic acid A  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP,ISO)
belinostat  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
bicalutamide  (EXP)
bisphenol A  (EXP,ISO)
Bisphenol A diglycidyl ether  (ISO)
bisphenol F  (ISO)
butanal  (EXP)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
calcitriol  (EXP)
capsaicin  (ISO)
carbamazepine  (ISO)
carbon nanotube  (ISO)
CGP 52608  (EXP)
choline  (ISO)
ciguatoxin CTX1B  (ISO)
cisplatin  (EXP)
clofibrate  (ISO)
cobalt dichloride  (EXP,ISO)
cocaine  (ISO)
copper atom  (EXP,ISO)
copper(0)  (EXP,ISO)
cyclophosphamide  (ISO)
cyclosporin A  (EXP)
cytarabine  (ISO)
depsipeptide  (EXP)
dexamethasone  (EXP)
dextran sulfate  (ISO)
dibutyl phthalate  (ISO)
diclofenac  (ISO)
dicrotophos  (EXP)
diethylstilbestrol  (ISO)
dioxygen  (ISO)
disodium selenite  (ISO)
disulfiram  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
entinostat  (EXP)
enzacamene  (EXP)
ethanol  (EXP,ISO)
fenthion  (ISO)
ferric oxide  (ISO)
flavonoids  (ISO)
folic acid  (ISO)
fulvestrant  (EXP)
furan  (ISO)
gemcitabine  (EXP)
genistein  (EXP)
gentamycin  (ISO)
graphite  (ISO)
hypochlorous acid  (ISO)
indoles  (ISO)
indometacin  (EXP)
ivermectin  (EXP)
L-methionine  (ISO)
leflunomide  (EXP,ISO)
manganese atom  (EXP)
manganese(0)  (EXP)
manganese(II) chloride  (EXP)
melphalan  (EXP)
mercury dibromide  (EXP)
methotrexate  (EXP)
Morroniside  (ISO)
N-acetylsphingosine  (EXP)
N-methyl-N'-nitro-N-nitrosoguanidine  (ISO)
naproxen  (ISO)
nickel dichloride  (ISO)
nitrobenzenes  (ISO)
oxaliplatin  (EXP,ISO)
p-menthan-3-ol  (EXP)
paclitaxel  (EXP)
panobinostat  (EXP)
paracetamol  (EXP,ISO)
PD 0325901  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (ISO)
phenylmercury acetate  (EXP)
pirinixic acid  (ISO)
piroxicam  (EXP)
pregnenolone 16alpha-carbonitrile  (ISO)
progesterone  (EXP)
propiconazole  (ISO)
Ptaquiloside  (ISO)
quercetin  (EXP)
rotenone  (EXP,ISO)
sarin  (EXP)
SB 431542  (EXP)
senecionine  (ISO)
serpentine asbestos  (EXP)
silicon dioxide  (ISO)
simvastatin  (EXP)
sodium arsenate  (EXP,ISO)
sodium arsenite  (ISO)
sodium dichromate  (EXP)
Soman  (ISO)
sotorasib  (EXP)
sphingosine 1-phosphate  (EXP)
succimer  (EXP,ISO)
sulfadimethoxine  (ISO)
sumatriptan  (ISO)
sunitinib  (EXP)
tamoxifen  (ISO)
temozolomide  (EXP)
Tesaglitazar  (ISO)
testosterone  (ISO)
tetrachloromethane  (ISO)
thalidomide  (EXP)
thioacetamide  (ISO)
titanium dioxide  (ISO)
toluene  (ISO)
toluene 2,4-diisocyanate  (ISO)
topotecan  (ISO)
trametinib  (EXP)
trichostatin A  (EXP)
triclosan  (EXP)
troglitazone  (EXP,ISO)
urethane  (EXP)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
zinc atom  (ISO)
zinc(0)  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
angiogenesis  (IEA,IMP,ISO,ISS)
angiogenesis involved in coronary vascular morphogenesis  (IEA,ISS)
animal organ morphogenesis  (TAS)
artery morphogenesis  (IEA,ISS)
axon extension  (IEA,ISO)
axon extension involved in axon guidance  (IEA,ISO,ISS)
axon guidance  (IBA,IEA,ISO,NAS,TAS)
axonal fasciculation  (IEA,ISO)
axonogenesis involved in innervation  (IEA,ISS)
basal dendrite arborization  (IEA,ISS)
basal dendrite development  (IEA,ISS)
blood vessel endothelial cell migration  (IEA,ISO)
branching involved in blood vessel morphogenesis  (IEA,ISO,ISS)
branchiomotor neuron axon guidance  (IEA,ISS)
cardiac neural crest cell migration involved in outflow tract morphogenesis  (ISO)
cell differentiation  (IEA)
cell migration involved in sprouting angiogenesis  (IEA,ISS)
cell-cell signaling  (TAS)
cellular response to hepatocyte growth factor stimulus  (IMP)
cellular response to vascular endothelial growth factor stimulus  (IEA,ISS)
commissural neuron axon guidance  (IEA,ISS)
coronary artery morphogenesis  (IEA)
dendrite development  (IEA,ISO)
dichotomous subdivision of terminal units involved in salivary gland branching  (IEA,ISO)
dorsal root ganglion morphogenesis  (IEA)
endothelial cell chemotaxis  (IMP)
endothelial cell migration  (IEA)
endothelial tip cell fate specification  (ISS)
facial nerve structural organization  (IEA,ISS)
facioacoustic ganglion development  (IEA)
gonadotrophin-releasing hormone neuronal migration to the hypothalamus  (IEA)
heart development  (IEA,ISO)
hepatocyte growth factor receptor signaling pathway  (IMP)
integrin-mediated signaling pathway  (IEA,IMP)
motor neuron axon guidance  (IEA,ISS)
motor neuron migration  (IEA,ISS)
negative regulation of axon extension  (IEA,ISO)
negative regulation of axon extension involved in axon guidance  (IEA,ISO)
negative regulation of extrinsic apoptotic signaling pathway  (IEA)
negative regulation of neuron apoptotic process  (IEA)
nervous system development  (IEA)
neural crest cell migration  (IBA,IEA)
neural crest cell migration involved in autonomic nervous system development  (IEA,ISS)
neuron development  (IEA)
neuron migration  (IEA,ISS)
neuropilin signaling pathway  (IEA,IMP)
otic placode development  (IEA)
outflow tract septum morphogenesis  (IEA,ISS)
platelet-derived growth factor receptor signaling pathway  (IMP)
positive chemotaxis  (IEA,ISS)
positive regulation of angiogenesis  (IEA)
positive regulation of axon extension involved in axon guidance  (IEA,ISS)
positive regulation of cell migration involved in sprouting angiogenesis  (IEA)
positive regulation of endothelial cell migration  (IBA,IEA,IMP,TAS)
positive regulation of endothelial cell proliferation  (TAS)
positive regulation of ERK1 and ERK2 cascade  (IEA,ISS)
positive regulation of filopodium assembly  (IBA,IEA,IMP)
positive regulation of focal adhesion assembly  (IDA)
positive regulation of peptidyl-tyrosine phosphorylation  (IEA)
positive regulation of phosphorylation  (IEA)
positive regulation of platelet-derived growth factor receptor signaling pathway  (ISO)
positive regulation of smooth muscle cell chemotaxis  (ISO)
positive regulation of smooth muscle cell migration  (TAS)
positive regulation of stress fiber assembly  (IMP)
positive regulation of substrate adhesion-dependent cell spreading  (IMP)
positive regulation of vascular associated smooth muscle cell migration  (ISO)
postsynapse organization  (IEA)
protein localization to early endosome  (IEA,ISS)
regulation of axon extension involved in axon guidance  (IEA,ISO)
regulation of Cdc42 protein signal transduction  (IEA,IMP)
regulation of plasma membrane bounded cell projection organization  (IEA)
regulation of vascular endothelial growth factor receptor signaling pathway  (IBA,IEA)
regulation of vesicle-mediated transport  (TAS)
renal artery morphogenesis  (IEA)
response to wounding  (IBA,IEA)
retina vasculature development in camera-type eye  (IEA,ISO)
retina vasculature morphogenesis in camera-type eye  (IEA,ISS)
retinal ganglion cell axon guidance  (IEA,ISS)
semaphorin-plexin signaling pathway  (IEA,ISO,ISS,NAS)
sensory neuron axon guidance  (IEA)
signal transduction  (TAS)
sprouting angiogenesis  (IBA,IEA,ISS)
substrate-dependent cell migration, cell extension  (IMP)
sympathetic ganglion development  (IEA,ISS)
sympathetic nervous system development  (IEA,ISO)
sympathetic neuron projection extension  (IEA,ISS)
sympathetic neuron projection guidance  (IEA,ISS)
trigeminal ganglion development  (IEA)
trigeminal nerve morphogenesis  (IEA,ISO)
trigeminal nerve structural organization  (IEA,ISS)
vascular endothelial growth factor receptor signaling pathway  (IBA,IEA,IMP,ISO)
vascular endothelial growth factor signaling pathway  (IEA)
vasculogenesis  (IBA,IEA)
VEGF-activated neuropilin signaling pathway  (IEA,IMP,ISS)
ventral trunk neural crest cell migration  (IEA)
vestibulocochlear nerve structural organization  (IEA)
wound healing  (ISO)

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Neuropilin-1 facilitates SARS-CoV-2 cell entry and infectivity. Cantuti-Castelvetri L, etal., Science. 2020 Nov 13;370(6518):856-860. doi: 10.1126/science.abd2985. Epub 2020 Oct 20.
2. Expression of VEGFR2 and NRP-1 in non-small cell lung cancer and their clinical significance. Ding M, etal., Chin J Cancer Res. 2014 Dec;26(6):669-77. doi: 10.3978/j.issn.1000-9604.2014.12.04.
3. Functional polymorphisms of the neuropilin 1 gene are associated with the risk of tetralogy of Fallot in a Chinese Han population. Fan SH, etal., Gene. 2018 May 5;653:72-79. doi: 10.1016/j.gene.2018.02.027. Epub 2018 Feb 10.
4. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
5. Effects of experimental type 1 diabetes and exercise training on angiogenic gene expression and capillarization in skeletal muscle. Kivela R, etal., FASEB J. 2006 Jul;20(9):1570-2.
6. Long non-coding RNA THRIL inhibits miRNA-24-3p to upregulate neuropilin-1 to aggravate cerebral ischemia-reperfusion injury through regulating the nuclear factor κB p65 signaling. Kuai F, etal., Aging (Albany NY). 2021 Mar 6;13(6):9071-9084. doi: 10.18632/aging.202762. Epub 2021 Mar 6.
7. Identifying New COVID-19 Receptor Neuropilin-1 in Severe Alzheimer's Disease Patients Group Brain Using Genome-Wide Association Study Approach. Lim KH, etal., Front Genet. 2021 Oct 21;12:741175. doi: 10.3389/fgene.2021.741175. eCollection 2021.
8. Molecular regulation of the VEGF family -- inducers of angiogenesis and lymphangiogenesis. McColl BK, etal., APMIS 2004 Jul-Aug;112(7-8):463-80.
9. Perivascular Neuropilin-1 expression is an independent marker of improved survival in renal cell carcinoma. Morin E, etal., J Pathol. 2020 Apr;250(4):387-396. doi: 10.1002/path.5380. Epub 2020 Jan 29.
10. VEGF receptor signalling - in control of vascular function. Olsson AK, etal., Nat Rev Mol Cell Biol. 2006 May;7(5):359-71.
11. Neuropilins 1 and 2 mediate neointimal hyperplasia and re-endothelialization following arterial injury. Pellet-Many C, etal., Cardiovasc Res. 2015 Nov 1;108(2):288-98. doi: 10.1093/cvr/cvv229. Epub 2015 Sep 25.
12. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
13. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
14. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
15. Nuclear translocation of UDCA by the glucocorticoid receptor is required to reduce TGF-beta1-induced apoptosis in rat hepatocytes. Sola S, etal., Hepatology. 2005 Oct;42(4):925-34.
16. The Neuropilin-1 Inhibitor, ATWLPPR Peptide, Prevents Experimental Diabetes-Induced Retinal Injury by Preserving Vascular Integrity and Decreasing Oxidative Stress. Wang J, etal., PLoS One. 2015 Nov 10;10(11):e0142571. doi: 10.1371/journal.pone.0142571. eCollection 2015.
17. SARS-CoV-2 infects human pancreatic β cells and elicits β cell impairment. Wu CT, etal., Cell Metab. 2021 Aug 3;33(8):1565-1576.e5. doi: 10.1016/j.cmet.2021.05.013. Epub 2021 May 18.
18. Ganoderma lucidum polysaccharides ameliorate lipopolysaccharide-induced acute pneumonia via inhibiting NRP1-mediated inflammation. Zhang X, etal., Pharm Biol. 2022 Dec;60(1):2201-2209. doi: 10.1080/13880209.2022.2142615.
19. Peritumoral Neuropilin-1 and VEGF receptor-2 expression increases time to recurrence in hepatocellular carcinoma patients undergoing curative hepatectomy. Zhuang PY, etal., Oncotarget. 2014 Nov 30;5(22):11121-32. doi: 10.18632/oncotarget.2553.
Additional References at PubMed
PMID:9288753   PMID:9331348   PMID:9529250   PMID:9856463   PMID:9883722   PMID:10196546   PMID:10329017   PMID:10409677   PMID:10414980   PMID:10520994   PMID:10520995   PMID:10688880  
PMID:10748121   PMID:10842181   PMID:11112349   PMID:11166270   PMID:11239433   PMID:11256614   PMID:11333271   PMID:11604131   PMID:11807987   PMID:11886873   PMID:11948691   PMID:11953749  
PMID:11976715   PMID:11986311   PMID:12216067   PMID:12456642   PMID:12477932   PMID:12517344   PMID:12577308   PMID:12730958   PMID:12883660   PMID:14500350   PMID:14514674   PMID:14600159  
PMID:14760080   PMID:15126502   PMID:15160992   PMID:15161648   PMID:15166498   PMID:15233640   PMID:15239958   PMID:15489334   PMID:15522955   PMID:15550623   PMID:15613413   PMID:15695515  
PMID:15920019   PMID:15956974   PMID:15978582   PMID:16159877   PMID:16330548   PMID:16335952   PMID:16344560   PMID:16371354   PMID:16377081   PMID:16385451   PMID:16423422   PMID:16424390  
PMID:16502470   PMID:16513643   PMID:16648151   PMID:16763549   PMID:16809290   PMID:16847823   PMID:16849452   PMID:16990775   PMID:17015762   PMID:17017185   PMID:17088944   PMID:17222790  
PMID:17369353   PMID:17369861   PMID:17376520   PMID:17575273   PMID:17726369   PMID:17891484   PMID:17917967   PMID:17974973   PMID:18000534   PMID:18065694   PMID:18088455   PMID:18164591  
PMID:18223683   PMID:18231921   PMID:18272814   PMID:18284215   PMID:18325345   PMID:18403014   PMID:18443354   PMID:18628209   PMID:18638267   PMID:18704117   PMID:18708346   PMID:18785001  
PMID:18922901   PMID:18974107   PMID:18984674   PMID:18996601   PMID:19037249   PMID:19054571   PMID:19086053   PMID:19175293   PMID:19270265   PMID:19364973   PMID:19460752   PMID:19474288  
PMID:19480842   PMID:19486891   PMID:19499532   PMID:19736548   PMID:19805273   PMID:19837659   PMID:19857463   PMID:19909241   PMID:20026901   PMID:20043119   PMID:20053475   PMID:20085644  
PMID:20201926   PMID:20215856   PMID:20363638   PMID:20577048   PMID:20588308   PMID:20631636   PMID:20675371   PMID:20950431   PMID:20956519   PMID:21063027   PMID:21111525   PMID:21186301  
PMID:21245381   PMID:21306301   PMID:21338642   PMID:21401950   PMID:21423176   PMID:21525791   PMID:21586748   PMID:21653826   PMID:21682944   PMID:21852397   PMID:21873635   PMID:21897119  
PMID:21939755   PMID:21951945   PMID:21978468   PMID:21988832   PMID:22025255   PMID:22052678   PMID:22134529   PMID:22251373   PMID:22318724   PMID:22393126   PMID:22627768   PMID:22683681  
PMID:22875653   PMID:22885184   PMID:22897854   PMID:23145112   PMID:23175449   PMID:23185562   PMID:23222303   PMID:23288161   PMID:23297363   PMID:23398358   PMID:23447383   PMID:23452854  
PMID:23455922   PMID:23551578   PMID:23585340   PMID:23621014   PMID:23639442   PMID:23685409   PMID:23793025   PMID:23956271   PMID:24021649   PMID:24053763   PMID:24066029   PMID:24079887  
PMID:24114198   PMID:24338507   PMID:24386482   PMID:24401374   PMID:24521511   PMID:24556756   PMID:24627131   PMID:24632553   PMID:24641672   PMID:24711643   PMID:24719187   PMID:24736504  
PMID:24737589   PMID:24791743   PMID:24850663   PMID:24858828   PMID:24863063   PMID:24992616   PMID:24999732   PMID:25077433   PMID:25180605   PMID:25204970   PMID:25231404   PMID:25233427  
PMID:25271625   PMID:25277522   PMID:25315821   PMID:25343644   PMID:25351619   PMID:25586548   PMID:25670642   PMID:25713110   PMID:25738638   PMID:25744030   PMID:25772243   PMID:25845525  
PMID:25889301   PMID:25954957   PMID:25979342   PMID:25997710   PMID:26037503   PMID:26051942   PMID:26147006   PMID:26186194   PMID:26191184   PMID:26371509   PMID:26406949   PMID:26408254  
PMID:26409917   PMID:26451046   PMID:26496610   PMID:26563279   PMID:26573160   PMID:26602825   PMID:26701889   PMID:26708340   PMID:26795388   PMID:26804163   PMID:26804176   PMID:26805761  
PMID:26823738   PMID:26846845   PMID:26849476   PMID:26877262   PMID:26923176   PMID:26937865   PMID:26967387   PMID:27014911   PMID:27117252   PMID:27257039   PMID:27351129   PMID:27481513  
PMID:27486976   PMID:27542226   PMID:27591257   PMID:27598321   PMID:27666723   PMID:27676403   PMID:27720589   PMID:27797376   PMID:27798666   PMID:27937055   PMID:28077445   PMID:28092670  
PMID:28254885   PMID:28468826   PMID:28514442   PMID:28552348   PMID:28607365   PMID:28611215   PMID:28618167   PMID:28636974   PMID:28692057   PMID:28835419   PMID:28910136   PMID:28938007  
PMID:29018205   PMID:29059172   PMID:29138851   PMID:29363855   PMID:29457037   PMID:29457830   PMID:29486132   PMID:29507755   PMID:29509190   PMID:29630862   PMID:29671086   PMID:29693748  
PMID:29728077   PMID:29750423   PMID:29755126   PMID:29777301   PMID:29790686   PMID:29852799   PMID:29953416   PMID:29956750   PMID:29966621   PMID:29971782   PMID:30021884   PMID:30027561  
PMID:30236477   PMID:30360368   PMID:30362630   PMID:30378132   PMID:30378769   PMID:30456845   PMID:30717262   PMID:30767669   PMID:30806307   PMID:30811684   PMID:30841447   PMID:30909144  
PMID:30978940   PMID:31030100   PMID:31060904   PMID:31282408   PMID:31369989   PMID:31379809   PMID:31420553   PMID:31533337   PMID:31539113   PMID:31572401   PMID:31664117   PMID:31740486  
PMID:31809209   PMID:31894269   PMID:31898520   PMID:31944572   PMID:32046395   PMID:32062451   PMID:32069143   PMID:32102436   PMID:32183142   PMID:32274611   PMID:32305590   PMID:32472711  
PMID:32657612   PMID:32707033   PMID:32801339   PMID:32869019   PMID:32904674   PMID:32945351   PMID:32951327   PMID:32988865   PMID:32988871   PMID:33000221   PMID:33002021   PMID:33005016  
PMID:33009246   PMID:33014187   PMID:33070092   PMID:33082294   PMID:33118184   PMID:33212964   PMID:33246692   PMID:33262463   PMID:33350850   PMID:33387827   PMID:33395426   PMID:33432783  
PMID:33461580   PMID:33528717   PMID:33647793   PMID:33753480   PMID:33761321   PMID:33858046   PMID:33858750   PMID:33876574   PMID:33884469   PMID:33942999   PMID:33961781   PMID:33987449  
PMID:34079125   PMID:34168096   PMID:34212534   PMID:34252269   PMID:34374639   PMID:34434074   PMID:34635175   PMID:34636164   PMID:34647407   PMID:34698100   PMID:34709727   PMID:34843522  
PMID:34903696   PMID:34961486   PMID:35041031   PMID:35078508   PMID:35384245   PMID:35696571   PMID:36043525   PMID:36069030   PMID:36157881   PMID:36193963   PMID:36215168   PMID:36244648  
PMID:36333630   PMID:36376373   PMID:36430655   PMID:36449624   PMID:36653359   PMID:36811396   PMID:36841806   PMID:36898370   PMID:37169211   PMID:37175499   PMID:37302087   PMID:37499664  
PMID:37511358   PMID:37513474   PMID:37656811   PMID:37702613   PMID:37823194   PMID:37875691   PMID:37878035   PMID:37943081   PMID:38220212   PMID:38324585  


Genomics

Comparative Map Data
NRP1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381033,177,493 - 33,334,667 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1033,177,492 - 33,336,262 (-)EnsemblGRCh38hg38GRCh38
GRCh371033,466,421 - 33,623,595 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361033,506,432 - 33,663,839 (-)NCBINCBI36Build 36hg18NCBI36
Build 341033,506,432 - 33,663,476NCBI
Celera1033,231,763 - 33,389,179 (-)NCBICelera
Cytogenetic Map10p11.22NCBI
HuRef1033,186,444 - 33,343,500 (-)NCBIHuRef
CHM1_11033,468,091 - 33,625,451 (-)NCBICHM1_1
T2T-CHM13v2.01033,206,293 - 33,375,463 (-)NCBIT2T-CHM13v2.0
Nrp1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm398129,085,553 - 129,231,957 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl8129,085,085 - 129,229,844 (+)EnsemblGRCm39 Ensembl
GRCm388128,358,591 - 128,505,476 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl8128,358,604 - 128,503,363 (+)EnsemblGRCm38mm10GRCm38
MGSCv378130,882,973 - 131,029,376 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv368131,228,923 - 131,389,437 (+)NCBIMGSCv36mm8
Celera8132,685,332 - 132,831,714 (+)NCBICelera
Cytogenetic Map8E2NCBI
cM Map875.78NCBI
Nrp1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81973,256,557 - 73,411,705 (+)NCBIGRCr8
mRatBN7.21956,359,455 - 56,514,628 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1956,359,455 - 56,513,633 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1963,149,364 - 63,302,459 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01964,009,290 - 64,162,389 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01966,091,958 - 66,245,057 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01961,332,351 - 61,486,166 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1961,332,351 - 61,485,858 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01971,984,687 - 72,138,092 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41958,332,004 - 58,487,686 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11958,337,063 - 58,492,741 (+)NCBI
Celera1955,693,756 - 55,846,090 (+)NCBICelera
Cytogenetic Map19q12NCBI
Nrp1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554624,101,999 - 4,241,012 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554624,101,997 - 4,241,012 (+)NCBIChiLan1.0ChiLan1.0
NRP1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2845,819,786 - 45,977,758 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11045,825,106 - 45,982,734 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01033,298,918 - 33,456,466 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11033,883,162 - 34,039,645 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1033,883,173 - 34,039,648 (-)Ensemblpanpan1.1panPan2
NRP1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.123,416,062 - 3,553,929 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl23,413,821 - 3,552,483 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha23,515,185 - 3,653,323 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.023,710,166 - 3,848,420 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl23,710,304 - 3,848,417 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.123,489,029 - 3,627,209 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.023,524,020 - 3,661,782 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.023,642,794 - 3,780,784 (+)NCBIUU_Cfam_GSD_1.0
Nrp1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934412,194,941 - 12,335,217 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365741,694,336 - 1,834,720 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365741,694,433 - 1,834,720 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NRP1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1056,280,665 - 56,430,777 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11056,280,673 - 56,430,832 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21061,651,758 - 61,802,358 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NRP1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1932,474,787 - 32,632,746 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl932,474,309 - 32,633,101 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605641,535,637 - 41,695,579 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nrp1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248058,438,498 - 8,574,508 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248058,438,485 - 8,574,845 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NRP1
98 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_003873.5(NRP1):c.1470G>A (p.Gly490=) single nucleotide variant Malignant melanoma [RCV000068922] Chr10:33213530 [GRCh38]
Chr10:33502458 [GRCh37]
Chr10:33542464 [NCBI36]
Chr10:10p11.22		 not provided
NM_003873.5(NRP1):c.957G>A (p.Glu319=) single nucleotide variant Malignant melanoma [RCV000068923] Chr10:33254052 [GRCh38]
Chr10:33542980 [GRCh37]
Chr10:33582986 [NCBI36]
Chr10:10p11.22		 not provided
NM_003873.5(NRP1):c.2363G>A (p.Gly788Glu) single nucleotide variant Malignant melanoma [RCV000062033] Chr10:33185696 [GRCh38]
Chr10:33474624 [GRCh37]
Chr10:33514630 [NCBI36]
Chr10:10p11.22		 not provided
NM_003873.5(NRP1):c.248+4988G>T single nucleotide variant Lung cancer [RCV000108952] Chr10:33325720 [GRCh38]
Chr10:33614648 [GRCh37]
Chr10:10p11.22		 uncertain significance
GRCh38/hg38 10p11.22-11.1(chr10:31999920-38119681)x3 copy number gain See cases [RCV000135414] Chr10:31999920..38119681 [GRCh38]
Chr10:32288848..38408609 [GRCh37]
Chr10:32328854..38448615 [NCBI36]
Chr10:10p11.22-11.1		 pathogenic
GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3 copy number gain See cases [RCV000141497] Chr10:4604734..48074662 [GRCh38]
Chr10:4646926..47531169 [GRCh37]
Chr10:4636926..47125152 [NCBI36]
Chr10:10p15.1-q11.22		 benign
NM_003873.7(NRP1):c.248+2T>G single nucleotide variant not provided [RCV000185633] Chr10:33330706 [GRCh38]
Chr10:33619634 [GRCh37]
Chr10:10p11.22		 uncertain significance
GRCh37/hg19 10p11.22-11.21(chr10:32323692-37520394)x3 copy number gain Breast ductal adenocarcinoma [RCV000207153] Chr10:32323692..37520394 [GRCh37]
Chr10:10p11.22-11.21		 uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3 copy number gain See cases [RCV000448750] Chr10:93297..135378918 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143) copy number gain See cases [RCV000511389] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic|uncertain significance
GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3 copy number gain See cases [RCV000510893] Chr10:100026..50961640 [GRCh37]
Chr10:10p15.3-q11.23		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3 copy number gain See cases [RCV000510861] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_003873.7(NRP1):c.2522A>G (p.Lys841Arg) single nucleotide variant Inborn genetic diseases [RCV003282398] Chr10:33180326 [GRCh38]
Chr10:33469254 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2518G>A (p.Asp840Asn) single nucleotide variant Inborn genetic diseases [RCV003249729] Chr10:33180330 [GRCh38]
Chr10:33469258 [GRCh37]
Chr10:10p11.22		 uncertain significance
Single allele deletion not provided [RCV000677961] Chr10:33254302..35641435 [GRCh38]
Chr10:33543230..35930363 [GRCh37]
Chr10:10p11.22-11.21		 uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3 copy number gain not provided [RCV000749464] Chr10:73232..135524321 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3 copy number gain not provided [RCV000749465] Chr10:98087..135477883 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_003873.7(NRP1):c.2349C>A (p.Gly783=) single nucleotide variant NRP1-related condition [RCV003913293]|not provided [RCV000949963] Chr10:33185710 [GRCh38]
Chr10:33474638 [GRCh37]
Chr10:10p11.22		 benign|likely benign
NM_003873.7(NRP1):c.1571C>T (p.Ser524Leu) single nucleotide variant NRP1-related condition [RCV003962874]|not provided [RCV000970713] Chr10:33213429 [GRCh38]
Chr10:33502357 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.2500G>A (p.Glu834Lys) single nucleotide variant NRP1-related condition [RCV003910734]|not provided [RCV000900265] Chr10:33180348 [GRCh38]
Chr10:33469276 [GRCh37]
Chr10:10p11.22		 benign|likely benign
NM_003873.7(NRP1):c.549A>G (p.Ser183=) single nucleotide variant NRP1-related condition [RCV003943106]|not provided [RCV000961166] Chr10:33263755 [GRCh38]
Chr10:33552683 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1467G>C (p.Leu489=) single nucleotide variant NRP1-related condition [RCV003928606]|not provided [RCV000976535] Chr10:33213533 [GRCh38]
Chr10:33502461 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.2645C>A (p.Ala882Asp) single nucleotide variant Inborn genetic diseases [RCV003271228] Chr10:33180203 [GRCh38]
Chr10:33469131 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.936G>C (p.Glu312Asp) single nucleotide variant NRP1-related condition [RCV003392914] Chr10:33254073 [GRCh38]
Chr10:33543001 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2483-3T>C single nucleotide variant NRP1-related condition [RCV003943020]|not provided [RCV000950186] Chr10:33180368 [GRCh38]
Chr10:33469296 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.418A>C (p.Ile140Leu) single nucleotide variant not provided [RCV000931194] Chr10:33270687 [GRCh38]
Chr10:33559615 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.800G>A (p.Ser267Asn) single nucleotide variant NRP1-related condition [RCV003970844]|not provided [RCV000964200] Chr10:33256330 [GRCh38]
Chr10:33545258 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.243C>T (p.Asp81=) single nucleotide variant NRP1-related condition [RCV003928498]|not provided [RCV000970860] Chr10:33330713 [GRCh38]
Chr10:33619641 [GRCh37]
Chr10:10p11.22		 benign
GRCh37/hg19 10p11.23-11.22(chr10:30624523-33688350)x1 copy number loss not provided [RCV001795544] Chr10:30624523..33688350 [GRCh37]
Chr10:10p11.23-11.22		 pathogenic
GRCh37/hg19 10p15.3-q11.22(chr10:135655-47688677)x4 copy number gain Mosaic supernumerary isodicentric chromosome 10 [RCV001825164] Chr10:135655..47688677 [GRCh37]
Chr10:10p15.3-q11.22		 not provided
GRCh37/hg19 10p15.1-11.21(chr10:6273934-34732521) copy number gain not specified [RCV002052863] Chr10:6273934..34732521 [GRCh37]
Chr10:10p15.1-11.21		 pathogenic
NM_003873.7(NRP1):c.1637A>T (p.Tyr546Phe) single nucleotide variant Inborn genetic diseases [RCV003282073] Chr10:33207694 [GRCh38]
Chr10:33496622 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1894C>T (p.Pro632Ser) single nucleotide variant Inborn genetic diseases [RCV002968343] Chr10:33197680 [GRCh38]
Chr10:33486608 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.235G>C (p.Asp79His) single nucleotide variant Inborn genetic diseases [RCV002729303] Chr10:33330721 [GRCh38]
Chr10:33619649 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1009A>G (p.Thr337Ala) single nucleotide variant Inborn genetic diseases [RCV002993210]|NRP1-related condition [RCV003420504] Chr10:33226262 [GRCh38]
Chr10:33515190 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2471T>C (p.Ile824Thr) single nucleotide variant Inborn genetic diseases [RCV002946935]|NRP1-related condition [RCV003963761] Chr10:33182709 [GRCh38]
Chr10:33471637 [GRCh37]
Chr10:10p11.22		 likely benign|uncertain significance
NM_003873.7(NRP1):c.2317T>C (p.Ser773Pro) single nucleotide variant Inborn genetic diseases [RCV002799745] Chr10:33186234 [GRCh38]
Chr10:33475162 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1483G>A (p.Val495Met) single nucleotide variant Inborn genetic diseases [RCV002661086] Chr10:33213517 [GRCh38]
Chr10:33502445 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.58G>A (p.Gly20Ser) single nucleotide variant Inborn genetic diseases [RCV002910840] Chr10:33334325 [GRCh38]
Chr10:33623253 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.475A>G (p.Lys159Glu) single nucleotide variant Inborn genetic diseases [RCV002911712] Chr10:33263829 [GRCh38]
Chr10:33552757 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2335G>C (p.Val779Leu) single nucleotide variant Inborn genetic diseases [RCV002910382] Chr10:33185724 [GRCh38]
Chr10:33474652 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1717G>A (p.Gly573Arg) single nucleotide variant Inborn genetic diseases [RCV002805234] Chr10:33207614 [GRCh38]
Chr10:33496542 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2120G>T (p.Arg707Leu) single nucleotide variant Inborn genetic diseases [RCV002673314] Chr10:33186431 [GRCh38]
Chr10:33475359 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.44T>C (p.Val15Ala) single nucleotide variant Inborn genetic diseases [RCV002668922] Chr10:33334339 [GRCh38]
Chr10:33623267 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1403G>A (p.Arg468His) single nucleotide variant Inborn genetic diseases [RCV002670547] Chr10:33213597 [GRCh38]
Chr10:33502525 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1684A>C (p.Ile562Leu) single nucleotide variant Inborn genetic diseases [RCV002898037] Chr10:33207647 [GRCh38]
Chr10:33496575 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1549A>G (p.Ile517Val) single nucleotide variant Inborn genetic diseases [RCV002897051] Chr10:33213451 [GRCh38]
Chr10:33502379 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1604G>C (p.Arg535Pro) single nucleotide variant Inborn genetic diseases [RCV003010552] Chr10:33213396 [GRCh38]
Chr10:33502324 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.194A>G (p.Gln65Arg) single nucleotide variant Inborn genetic diseases [RCV002655263]|NRP1-related condition [RCV003410144] Chr10:33330762 [GRCh38]
Chr10:33619690 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1654C>T (p.Arg552Trp) single nucleotide variant Inborn genetic diseases [RCV002725131]|NRP1-related condition [RCV003946411] Chr10:33207677 [GRCh38]
Chr10:33496605 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1076A>T (p.Lys359Met) single nucleotide variant Inborn genetic diseases [RCV003206235] Chr10:33226195 [GRCh38]
Chr10:33515123 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2299C>T (p.Arg767Cys) single nucleotide variant Inborn genetic diseases [RCV003213314] Chr10:33186252 [GRCh38]
Chr10:33475180 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1567G>A (p.Gly523Ser) single nucleotide variant Inborn genetic diseases [RCV003195347] Chr10:33213433 [GRCh38]
Chr10:33502361 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1552G>A (p.Gly518Arg) single nucleotide variant Inborn genetic diseases [RCV003201307] Chr10:33213448 [GRCh38]
Chr10:33502376 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1041A>C (p.Lys347Asn) single nucleotide variant Inborn genetic diseases [RCV003203831] Chr10:33226230 [GRCh38]
Chr10:33515158 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1445A>G (p.Asn482Ser) single nucleotide variant Inborn genetic diseases [RCV003283242] Chr10:33213555 [GRCh38]
Chr10:33502483 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1789G>A (p.Gly597Arg) single nucleotide variant Inborn genetic diseases [RCV003207963] Chr10:33202966 [GRCh38]
Chr10:33491894 [GRCh37]
Chr10:10p11.22		 uncertain significance
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143) copy number gain Distal trisomy 10q [RCV003319593] Chr10:11138692..135427143 [GRCh37]
Chr10:10p14-q26.3		 pathogenic
NM_003873.7(NRP1):c.2502A>T (p.Glu834Asp) single nucleotide variant Inborn genetic diseases [RCV003309259] Chr10:33180346 [GRCh38]
Chr10:33469274 [GRCh37]
Chr10:10p11.22		 uncertain significance
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143) copy number loss Distal 10q deletion syndrome [RCV003319583] Chr10:12829206..135427143 [GRCh37]
Chr10:10p13-q26.3		 pathogenic
NM_003873.7(NRP1):c.2762C>T (p.Ser921Leu) single nucleotide variant Inborn genetic diseases [RCV003358818] Chr10:33180086 [GRCh38]
Chr10:33469014 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.466G>A (p.Gly156Arg) single nucleotide variant NRP1-related condition [RCV003420766] Chr10:33263838 [GRCh38]
Chr10:33552766 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.49G>T (p.Ala17Ser) single nucleotide variant NRP1-related condition [RCV003393243] Chr10:33334334 [GRCh38]
Chr10:33623262 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2629G>T (p.Val877Phe) single nucleotide variant Inborn genetic diseases [RCV003366348] Chr10:33180219 [GRCh38]
Chr10:33469147 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.92T>C (p.Ile31Thr) single nucleotide variant NRP1-related condition [RCV003405934] Chr10:33330864 [GRCh38]
Chr10:33619792 [GRCh37]
Chr10:10p11.22		 uncertain significance
GRCh37/hg19 10p11.22-11.21(chr10:32617120-36913676)x1 copy number loss not provided [RCV003483089] Chr10:32617120..36913676 [GRCh37]
Chr10:10p11.22-11.21		 uncertain significance
NM_003873.7(NRP1):c.1759+1317G>A single nucleotide variant not provided [RCV003456702] Chr10:33206255 [GRCh38]
Chr10:33495183 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.920G>T (p.Arg307Leu) single nucleotide variant NRP1-related condition [RCV003399694] Chr10:33254089 [GRCh38]
Chr10:33543017 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1000C>T (p.Arg334Cys) single nucleotide variant NRP1-related condition [RCV003402857] Chr10:33226271 [GRCh38]
Chr10:33515199 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1626C>T (p.Gly542=) single nucleotide variant NRP1-related condition [RCV003399470] Chr10:33207705 [GRCh38]
Chr10:33496633 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1459A>G (p.Ile487Val) single nucleotide variant NRP1-related condition [RCV003429044] Chr10:33213541 [GRCh38]
Chr10:33502469 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1096G>A (p.Gly366Arg) single nucleotide variant NRP1-related condition [RCV003419155] Chr10:33226175 [GRCh38]
Chr10:33515103 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1010C>T (p.Thr337Met) single nucleotide variant NRP1-related condition [RCV003402866] Chr10:33226261 [GRCh38]
Chr10:33515189 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.605G>C (p.Gly202Ala) single nucleotide variant NRP1-related condition [RCV003412089] Chr10:33263699 [GRCh38]
Chr10:33552627 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.465T>A (p.Ser155Arg) single nucleotide variant NRP1-related condition [RCV003427766] Chr10:33263839 [GRCh38]
Chr10:33552767 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.664C>T (p.Pro222Ser) single nucleotide variant NRP1-related condition [RCV003414267] Chr10:33256466 [GRCh38]
Chr10:33545394 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.248+3_248+6del microsatellite NRP1-related condition [RCV003402723] Chr10:33330702..33330705 [GRCh38]
Chr10:33619630..33619633 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2632G>A (p.Val878Met) single nucleotide variant NRP1-related condition [RCV003402846] Chr10:33180216 [GRCh38]
Chr10:33469144 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1609G>A (p.Ala537Thr) single nucleotide variant NRP1-related condition [RCV003405801] Chr10:33213391 [GRCh38]
Chr10:33502319 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1676C>T (p.Thr559Met) single nucleotide variant NRP1-related condition [RCV003414514] Chr10:33207655 [GRCh38]
Chr10:33496583 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1517G>A (p.Arg506Gln) single nucleotide variant NRP1-related condition [RCV003410666] Chr10:33213483 [GRCh38]
Chr10:33502411 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1214G>A (p.Arg405Gln) single nucleotide variant NRP1-related condition [RCV003418772] Chr10:33221787 [GRCh38]
Chr10:33510715 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2571C>G (p.Ile857Met) single nucleotide variant NRP1-related condition [RCV003418747] Chr10:33180277 [GRCh38]
Chr10:33469205 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.127G>A (p.Gly43Ser) single nucleotide variant NRP1-related condition [RCV003429071] Chr10:33330829 [GRCh38]
Chr10:33619757 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2222G>A (p.Arg741His) single nucleotide variant NRP1-related condition [RCV003410593] Chr10:33186329 [GRCh38]
Chr10:33475257 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2696A>G (p.Tyr899Cys) single nucleotide variant NRP1-related condition [RCV003410683] Chr10:33180152 [GRCh38]
Chr10:33469080 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.365A>C (p.Lys122Thr) single nucleotide variant NRP1-related condition [RCV003417160] Chr10:33270740 [GRCh38]
Chr10:33559668 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.914G>A (p.Arg305His) single nucleotide variant NRP1-related condition [RCV003399592] Chr10:33254095 [GRCh38]
Chr10:33543023 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.602C>T (p.Pro201Leu) single nucleotide variant NRP1-related condition [RCV003402955] Chr10:33263702 [GRCh38]
Chr10:33552630 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.*6G>A single nucleotide variant NRP1-related condition [RCV003939574] Chr10:33180070 [GRCh38]
Chr10:33468998 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.271G>A (p.Asp91Asn) single nucleotide variant NRP1-related condition [RCV003892243] Chr10:33270834 [GRCh38]
Chr10:33559762 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2631C>A (p.Val877=) single nucleotide variant NRP1-related condition [RCV003971379] Chr10:33180217 [GRCh38]
Chr10:33469145 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.249-6T>C single nucleotide variant NRP1-related condition [RCV003894759] Chr10:33270862 [GRCh38]
Chr10:33559790 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2197G>A (p.Val733Ile) single nucleotide variant NRP1-related condition [RCV003972184] Chr10:33186354 [GRCh38]
Chr10:33475282 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.456A>G (p.Thr152=) single nucleotide variant NRP1-related condition [RCV003967081] Chr10:33263848 [GRCh38]
Chr10:33552776 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.720G>C (p.Ser240=) single nucleotide variant NRP1-related condition [RCV003902260] Chr10:33256410 [GRCh38]
Chr10:33545338 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2595T>C (p.Ser865=) single nucleotide variant NRP1-related condition [RCV003974329] Chr10:33180253 [GRCh38]
Chr10:33469181 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.867C>T (p.Asp289=) single nucleotide variant NRP1-related condition [RCV003904422] Chr10:33254142 [GRCh38]
Chr10:33543070 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2040G>A (p.Thr680=) single nucleotide variant NRP1-related condition [RCV003947333] Chr10:33192303 [GRCh38]
Chr10:33481231 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.381C>T (p.Tyr127=) single nucleotide variant NRP1-related condition [RCV003956914] Chr10:33270724 [GRCh38]
Chr10:33559652 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.747C>T (p.Thr249=) single nucleotide variant NRP1-related condition [RCV003979197] Chr10:33256383 [GRCh38]
Chr10:33545311 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.1572G>T (p.Ser524=) single nucleotide variant NRP1-related condition [RCV003983618] Chr10:33213428 [GRCh38]
Chr10:33502356 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1109T>C (p.Ile370Thr) single nucleotide variant NRP1-related condition [RCV003901946] Chr10:33226162 [GRCh38]
Chr10:33515090 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1925-3A>C single nucleotide variant NRP1-related condition [RCV003901975] Chr10:33192421 [GRCh38]
Chr10:33481349 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1611G>A (p.Ala537=) single nucleotide variant NRP1-related condition [RCV003967303] Chr10:33213389 [GRCh38]
Chr10:33502317 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1788C>T (p.Asn596=) single nucleotide variant NRP1-related condition [RCV003959030] Chr10:33202967 [GRCh38]
Chr10:33491895 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1161C>T (p.Pro387=) single nucleotide variant NRP1-related condition [RCV003984703] Chr10:33221840 [GRCh38]
Chr10:33510768 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.2355C>T (p.Ile785=) single nucleotide variant NRP1-related condition [RCV003904756] Chr10:33185704 [GRCh38]
Chr10:33474632 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1760C>T (p.Ala587Val) single nucleotide variant NRP1-related condition [RCV003977090] Chr10:33202995 [GRCh38]
Chr10:33491923 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1263A>G (p.Val421=) single nucleotide variant NRP1-related condition [RCV003921745] Chr10:33221738 [GRCh38]
Chr10:33510666 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1704A>G (p.Arg568=) single nucleotide variant NRP1-related condition [RCV003952266] Chr10:33207627 [GRCh38]
Chr10:33496555 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1029C>T (p.Gly343=) single nucleotide variant NRP1-related condition [RCV003937322] Chr10:33226242 [GRCh38]
Chr10:33515170 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.620G>A (p.Arg207His) single nucleotide variant NRP1-related condition [RCV003894367] Chr10:33263684 [GRCh38]
Chr10:33552612 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.2262G>A (p.Met754Ile) single nucleotide variant NRP1-related condition [RCV003921598] Chr10:33186289 [GRCh38]
Chr10:33475217 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.74-4G>C single nucleotide variant NRP1-related condition [RCV003921722] Chr10:33330886 [GRCh38]
Chr10:33619814 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.258C>T (p.Tyr86=) single nucleotide variant NRP1-related condition [RCV003962258] Chr10:33270847 [GRCh38]
Chr10:33559775 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.687A>G (p.Gly229=) single nucleotide variant NRP1-related condition [RCV003927124] Chr10:33256443 [GRCh38]
Chr10:33545371 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2192C>T (p.Ser731Phe) single nucleotide variant NRP1-related condition [RCV003901425] Chr10:33186359 [GRCh38]
Chr10:33475287 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.29C>T (p.Ala10Val) single nucleotide variant NRP1-related condition [RCV003901813] Chr10:33334354 [GRCh38]
Chr10:33623282 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1683C>G (p.Phe561Leu) single nucleotide variant NRP1-related condition [RCV003932206] Chr10:33207648 [GRCh38]
Chr10:33496576 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.1938T>C (p.Tyr646=) single nucleotide variant NRP1-related condition [RCV003896298] Chr10:33192405 [GRCh38]
Chr10:33481333 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1095C>T (p.Asn365=) single nucleotide variant NRP1-related condition [RCV003979796] Chr10:33226176 [GRCh38]
Chr10:33515104 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1497C>A (p.Ile499=) single nucleotide variant NRP1-related condition [RCV003911364] Chr10:33213503 [GRCh38]
Chr10:33502431 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1720C>G (p.Leu574Val) single nucleotide variant NRP1-related condition [RCV003904701] Chr10:33207611 [GRCh38]
Chr10:33496539 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2343C>T (p.Phe781=) single nucleotide variant NRP1-related condition [RCV003976515] Chr10:33185716 [GRCh38]
Chr10:33474644 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.2196C>A (p.His732Gln) single nucleotide variant NRP1-related condition [RCV003954805] Chr10:33186355 [GRCh38]
Chr10:33475283 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1797G>A (p.Leu599=) single nucleotide variant NRP1-related condition [RCV003964303] Chr10:33202958 [GRCh38]
Chr10:33491886 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1011G>A (p.Thr337=) single nucleotide variant NRP1-related condition [RCV003954936] Chr10:33226260 [GRCh38]
Chr10:33515188 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2431+3A>G single nucleotide variant NRP1-related condition [RCV003952200] Chr10:33185625 [GRCh38]
Chr10:33474553 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1898C>T (p.Thr633Met) single nucleotide variant NRP1-related condition [RCV003899375] Chr10:33197676 [GRCh38]
Chr10:33486604 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.60C>T (p.Gly20=) single nucleotide variant NRP1-related condition [RCV003964445] Chr10:33334323 [GRCh38]
Chr10:33623251 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.531C>A (p.Val177=) single nucleotide variant NRP1-related condition [RCV003929696] Chr10:33263773 [GRCh38]
Chr10:33552701 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2349C>T (p.Gly783=) single nucleotide variant NRP1-related condition [RCV003981359] Chr10:33185710 [GRCh38]
Chr10:33474638 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1815C>T (p.Asp605=) single nucleotide variant NRP1-related condition [RCV003904653] Chr10:33202940 [GRCh38]
Chr10:33491868 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.227A>G (p.Asp76Gly) single nucleotide variant NRP1-related condition [RCV003907252] Chr10:33330729 [GRCh38]
Chr10:33619657 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1062T>C (p.Tyr354=) single nucleotide variant NRP1-related condition [RCV003934453] Chr10:33226209 [GRCh38]
Chr10:33515137 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1266C>T (p.Tyr422=) single nucleotide variant NRP1-related condition [RCV003982434] Chr10:33221735 [GRCh38]
Chr10:33510663 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.249-9G>C single nucleotide variant NRP1-related condition [RCV003943910] Chr10:33270865 [GRCh38]
Chr10:33559793 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1566C>T (p.Asn522=) single nucleotide variant NRP1-related condition [RCV003911416] Chr10:33213434 [GRCh38]
Chr10:33502362 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1551C>T (p.Ile517=) single nucleotide variant NRP1-related condition [RCV003947126] Chr10:33213449 [GRCh38]
Chr10:33502377 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1800G>A (p.Val600=) single nucleotide variant NRP1-related condition [RCV003944001] Chr10:33202955 [GRCh38]
Chr10:33491883 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.72C>T (p.Asn24=) single nucleotide variant NRP1-related condition [RCV003911740] Chr10:33334311 [GRCh38]
Chr10:33623239 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2490G>A (p.Thr830=) single nucleotide variant NRP1-related condition [RCV003919723] Chr10:33180358 [GRCh38]
Chr10:33469286 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.1572G>A (p.Ser524=) single nucleotide variant NRP1-related condition [RCV003899038] Chr10:33213428 [GRCh38]
Chr10:33502356 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2562A>G (p.Leu854=) single nucleotide variant NRP1-related condition [RCV003893863] Chr10:33180286 [GRCh38]
Chr10:33469214 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.720G>A (p.Ser240=) single nucleotide variant NRP1-related condition [RCV003894023] Chr10:33256410 [GRCh38]
Chr10:33545338 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2088A>G (p.Gln696=) single nucleotide variant NRP1-related condition [RCV003971941] Chr10:33186463 [GRCh38]
Chr10:33475391 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.2062+5C>T single nucleotide variant NRP1-related condition [RCV003957241] Chr10:33192276 [GRCh38]
Chr10:33481204 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.221A>T (p.His74Leu) single nucleotide variant NRP1-related condition [RCV003901662] Chr10:33330735 [GRCh38]
Chr10:33619663 [GRCh37]
Chr10:10p11.22		 uncertain significance
NM_003873.7(NRP1):c.1295C>T (p.Ser432Phe) single nucleotide variant NRP1-related condition [RCV003921970] Chr10:33213705 [GRCh38]
Chr10:33502633 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.1425C>T (p.Pro475=) single nucleotide variant NRP1-related condition [RCV003896985] Chr10:33213575 [GRCh38]
Chr10:33502503 [GRCh37]
Chr10:10p11.22		 likely benign
NM_003873.7(NRP1):c.537G>A (p.Val179=) single nucleotide variant NRP1-related condition [RCV003974623] Chr10:33263767 [GRCh38]
Chr10:33552695 [GRCh37]
Chr10:10p11.22		 benign
NM_003873.7(NRP1):c.1738C>T (p.Leu580=) single nucleotide variant NRP1-related condition [RCV003976621] Chr10:33207593 [GRCh38]
Chr10:33496521 [GRCh37]
Chr10:10p11.22		 benign
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR320Ahsa-miR-320aOncomiRDBexternal_infoNANA22134529

Predicted Target Of
Summary Value
Count of predictions:5703
Count of miRNA genes:1308
Interacting mature miRNAs:1670
Transcripts:ENST00000265371, ENST00000374816, ENST00000374821, ENST00000374822, ENST00000374823, ENST00000374867, ENST00000374875, ENST00000395995, ENST00000413802, ENST00000418675, ENST00000431894, ENST00000432372, ENST00000455749, ENST00000466932
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
D10S1654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,527,692 - 33,527,946UniSTSGRCh37
Build 361033,567,698 - 33,567,952RGDNCBI36
Celera1033,293,041 - 33,293,295RGD
Cytogenetic Map10p12UniSTS
HuRef1033,247,714 - 33,247,968UniSTS
Marshfield Genetic Map1062.23RGD
Marshfield Genetic Map1062.23UniSTS
Genethon Genetic Map1062.0UniSTS
deCODE Assembly Map1060.46UniSTS
Whitehead-YAC Contig Map10 UniSTS
RH45612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,549,130 - 33,549,250UniSTSGRCh37
Build 361033,589,136 - 33,589,256RGDNCBI36
Celera1033,314,477 - 33,314,597RGD
Cytogenetic Map10p12UniSTS
HuRef1033,269,163 - 33,269,283UniSTS
GeneMap99-GB4 RH Map10183.94UniSTS
NCBI RH Map10429.9UniSTS
G20549  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,466,465 - 33,466,612UniSTSGRCh37
Build 361033,506,471 - 33,506,618RGDNCBI36
Celera1033,231,809 - 33,231,956RGD
Cytogenetic Map10p12UniSTS
HuRef1033,186,490 - 33,186,637UniSTS
A005W14  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,466,465 - 33,466,612UniSTSGRCh37
Build 361033,506,471 - 33,506,618RGDNCBI36
Celera1033,231,809 - 33,231,956RGD
Cytogenetic Map10p12UniSTS
HuRef1033,186,490 - 33,186,637UniSTS
GeneMap99-GB4 RH Map10196.22UniSTS
NCBI RH Map10501.1UniSTS
G48212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,530,085 - 33,530,190UniSTSGRCh37
Build 361033,570,091 - 33,570,196RGDNCBI36
Celera1033,295,434 - 33,295,539RGD
Cytogenetic Map10p12UniSTS
HuRef1033,250,107 - 33,250,212UniSTS
TNG Radiation Hybrid Map1017335.0UniSTS
RH120752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,500,205 - 33,500,492UniSTSGRCh37
Build 361033,540,211 - 33,540,498RGDNCBI36
Celera1033,265,557 - 33,265,844RGD
Cytogenetic Map10p12UniSTS
HuRef1033,220,236 - 33,220,523UniSTS
TNG Radiation Hybrid Map1017362.0UniSTS
RH122665  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,592,373 - 33,592,650UniSTSGRCh37
Build 361033,632,379 - 33,632,656RGDNCBI36
Celera1033,357,720 - 33,357,997RGD
Cytogenetic Map10p12UniSTS
HuRef1033,312,168 - 33,312,445UniSTS
TNG Radiation Hybrid Map1017285.0UniSTS
RH118801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,554,880 - 33,555,209UniSTSGRCh37
Build 361033,594,886 - 33,595,215RGDNCBI36
Celera1033,320,229 - 33,320,558RGD
Cytogenetic Map10p12UniSTS
HuRef1033,274,914 - 33,275,243UniSTS
TNG Radiation Hybrid Map1017327.0UniSTS
RH65747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,481,975 - 33,482,149UniSTSGRCh37
Build 361033,521,981 - 33,522,155RGDNCBI36
Celera1033,247,324 - 33,247,498RGD
Cytogenetic Map10p12UniSTS
HuRef1033,202,005 - 33,202,179UniSTS
GeneMap99-GB4 RH Map10194.71UniSTS
NCBI RH Map10501.1UniSTS
RH70034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,486,919 - 33,487,155UniSTSGRCh37
Build 361033,526,925 - 33,527,161RGDNCBI36
Celera1033,252,268 - 33,252,505RGD
Cytogenetic Map10p12UniSTS
GeneMap99-GB4 RH Map10195.03UniSTS
NCBI RH Map10501.1UniSTS
SHGC-56598  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,579,330 - 33,579,419UniSTSGRCh37
Build 361033,619,336 - 33,619,425RGDNCBI36
Celera1033,344,677 - 33,344,766RGD
Cytogenetic Map10p12UniSTS
HuRef1033,299,125 - 33,299,214UniSTS
TNG Radiation Hybrid Map1017302.0UniSTS
RH46501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371033,524,794 - 33,524,924UniSTSGRCh37
Build 361033,564,800 - 33,564,930RGDNCBI36
Celera1033,290,143 - 33,290,273RGD
Cytogenetic Map10p12UniSTS
HuRef1033,244,813 - 33,244,943UniSTS
GeneMap99-GB4 RH Map10194.71UniSTS
NCBI RH Map10501.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1546 2029 1179 312 383 225 2619 1273 842 337 869 1505 101 1204 1693 4
Low 875 290 545 312 326 240 1719 915 2718 81 575 90 73 1 1095 1 2
Below cutoff 13 664 1 828 16 8 173 1 12 12

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_030328 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001024628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001024629 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001244972 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001244973 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001330068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003873 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_045259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006717521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006717522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006717524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006717525 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006717526 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519755 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016865 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425976 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425977 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425978 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367071 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367072 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367074 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367075 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367076 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367078 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367079 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367080 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA973607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB209641 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF016050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF018956 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF086016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF145712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF268691 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF280547 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF482431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH010078 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL121748 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL353600 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL698999 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833608 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY249243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC007533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC007737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT006995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU858030 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX510902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648250 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471072 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749333 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA702852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU332859 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JC231892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782865 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782867 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782870 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782871 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782872 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782873 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782874 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782903 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782908 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782909 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC782911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784282 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784288 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784294 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC784296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MW962304 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000265371   ⟹   ENSP00000265371
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,177,492 - 33,336,262 (-)Ensembl
RefSeq Acc Id: ENST00000374816   ⟹   ENSP00000363949
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,205,449 - 33,334,522 (-)Ensembl
RefSeq Acc Id: ENST00000374821   ⟹   ENSP00000363954
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,197,621 - 33,334,522 (-)Ensembl
RefSeq Acc Id: ENST00000374822   ⟹   ENSP00000363955
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,197,621 - 33,334,642 (-)Ensembl
RefSeq Acc Id: ENST00000374823   ⟹   ENSP00000363956
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,201,018 - 33,334,382 (-)Ensembl
RefSeq Acc Id: ENST00000374867   ⟹   ENSP00000364001
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,177,493 - 33,334,667 (-)Ensembl
RefSeq Acc Id: ENST00000374875   ⟹   ENSP00000364009
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,177,492 - 33,334,636 (-)Ensembl
RefSeq Acc Id: ENST00000395995   ⟹   ENSP00000379317
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,177,494 - 33,334,905 (-)Ensembl
RefSeq Acc Id: ENST00000413802   ⟹   ENSP00000390447
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,179,897 - 33,185,655 (-)Ensembl
RefSeq Acc Id: ENST00000418675   ⟹   ENSP00000416147
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,194,367 - 33,202,995 (-)Ensembl
RefSeq Acc Id: ENST00000431894   ⟹   ENSP00000393071
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,195,424 - 33,207,625 (-)Ensembl
RefSeq Acc Id: ENST00000432372   ⟹   ENSP00000408911
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,211,410 - 33,335,078 (-)Ensembl
RefSeq Acc Id: ENST00000455749   ⟹   ENSP00000390567
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,249,414 - 33,263,704 (-)Ensembl
RefSeq Acc Id: ENST00000466932   ⟹   ENSP00000476896
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1033,194,372 - 33,213,561 (-)Ensembl
RefSeq Acc Id: NM_001024628   ⟹   NP_001019799
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,197,621 - 33,334,667 (-)NCBI
GRCh371033,466,419 - 33,623,833 (-)ENTREZGENE
Build 361033,526,557 - 33,663,576 (-)NCBI Archive
HuRef1033,186,444 - 33,343,500 (-)ENTREZGENE
CHM1_11033,488,221 - 33,625,451 (-)NCBI
T2T-CHM13v2.01033,226,424 - 33,363,487 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001024629   ⟹   NP_001019800
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,197,621 - 33,334,667 (-)NCBI
GRCh371033,466,419 - 33,623,833 (-)ENTREZGENE
Build 361033,526,555 - 33,663,456 (-)NCBI Archive
HuRef1033,186,444 - 33,343,500 (-)ENTREZGENE
CHM1_11033,488,221 - 33,625,451 (-)NCBI
T2T-CHM13v2.01033,226,424 - 33,363,487 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001244972   ⟹   NP_001231901
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
GRCh371033,466,419 - 33,623,833 (-)NCBI
HuRef1033,186,444 - 33,343,500 (-)NCBI
CHM1_11033,468,091 - 33,625,451 (-)NCBI
T2T-CHM13v2.01033,206,293 - 33,363,487 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001244973   ⟹   NP_001231902
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
GRCh371033,466,419 - 33,623,833 (-)NCBI
HuRef1033,186,444 - 33,343,500 (-)NCBI
CHM1_11033,468,091 - 33,625,451 (-)NCBI
T2T-CHM13v2.01033,206,293 - 33,363,487 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001330068   ⟹   NP_001316997
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
T2T-CHM13v2.01033,206,293 - 33,363,487 (-)NCBI
Sequence:
RefSeq Acc Id: NM_003873   ⟹   NP_003864
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
GRCh371033,466,419 - 33,623,833 (-)ENTREZGENE
Build 361033,506,432 - 33,663,839 (-)NCBI Archive
HuRef1033,186,444 - 33,343,500 (-)ENTREZGENE
CHM1_11033,468,091 - 33,625,451 (-)NCBI
T2T-CHM13v2.01033,206,293 - 33,363,487 (-)NCBI
Sequence:
RefSeq Acc Id: NR_045259
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
GRCh371033,466,419 - 33,623,833 (-)NCBI
HuRef1033,186,444 - 33,343,500 (-)NCBI
CHM1_11033,468,091 - 33,625,451 (-)NCBI
T2T-CHM13v2.01033,206,293 - 33,363,487 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006717521   ⟹   XP_006717584
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006717522   ⟹   XP_006717585
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006717524   ⟹   XP_006717587
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006717525   ⟹   XP_006717588
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006717526   ⟹   XP_006717589
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,194,383 - 33,334,667 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519755   ⟹   XP_011518057
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,194,383 - 33,334,667 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519756   ⟹   XP_011518058
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,194,383 - 33,334,667 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017016865   ⟹   XP_016872354
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047425976   ⟹   XP_047281932
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
RefSeq Acc Id: XM_047425977   ⟹   XP_047281933
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,334,667 (-)NCBI
RefSeq Acc Id: XM_047425978   ⟹   XP_047281934
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,177,493 - 33,330,846 (-)NCBI
RefSeq Acc Id: XM_054367070   ⟹   XP_054223045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367071   ⟹   XP_054223046
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367072   ⟹   XP_054223047
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,420 (-)NCBI
RefSeq Acc Id: XM_054367073   ⟹   XP_054223048
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,365,079 (-)NCBI
RefSeq Acc Id: XM_054367074   ⟹   XP_054223049
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,348 (-)NCBI
RefSeq Acc Id: XM_054367075   ⟹   XP_054223050
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367076   ⟹   XP_054223051
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,495 (-)NCBI
RefSeq Acc Id: XM_054367077   ⟹   XP_054223052
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,451 (-)NCBI
RefSeq Acc Id: XM_054367078   ⟹   XP_054223053
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,375,463 (-)NCBI
RefSeq Acc Id: XM_054367079   ⟹   XP_054223054
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367080   ⟹   XP_054223055
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367081   ⟹   XP_054223056
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,452 (-)NCBI
RefSeq Acc Id: XM_054367082   ⟹   XP_054223057
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367083   ⟹   XP_054223058
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,385 (-)NCBI
RefSeq Acc Id: XM_054367084   ⟹   XP_054223059
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,363,487 (-)NCBI
RefSeq Acc Id: XM_054367085   ⟹   XP_054223060
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,363,487 (-)NCBI
RefSeq Acc Id: XM_054367086   ⟹   XP_054223061
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367087   ⟹   XP_054223062
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367088   ⟹   XP_054223063
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367089   ⟹   XP_054223064
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,364,385 (-)NCBI
RefSeq Acc Id: XM_054367090   ⟹   XP_054223065
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,206,293 - 33,363,487 (-)NCBI
RefSeq Acc Id: XM_054367091   ⟹   XP_054223066
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,223,170 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367092   ⟹   XP_054223067
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,223,170 - 33,364,044 (-)NCBI
RefSeq Acc Id: XM_054367093   ⟹   XP_054223068
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01033,223,170 - 33,363,487 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001019799 (Get FASTA)   NCBI Sequence Viewer  
  NP_001019800 (Get FASTA)   NCBI Sequence Viewer  
  NP_001231901 (Get FASTA)   NCBI Sequence Viewer  
  NP_001231902 (Get FASTA)   NCBI Sequence Viewer  
  NP_001316997 (Get FASTA)   NCBI Sequence Viewer  
  NP_003864 (Get FASTA)   NCBI Sequence Viewer  
  XP_006717584 (Get FASTA)   NCBI Sequence Viewer  
  XP_006717585 (Get FASTA)   NCBI Sequence Viewer  
  XP_006717587 (Get FASTA)   NCBI Sequence Viewer  
  XP_006717588 (Get FASTA)   NCBI Sequence Viewer  
  XP_006717589 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518057 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518058 (Get FASTA)   NCBI Sequence Viewer  
  XP_016872354 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281932 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281933 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281934 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223045 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223046 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223047 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223048 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223049 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223050 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223051 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223052 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223053 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223054 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223055 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223056 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223057 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223058 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223059 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223060 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223061 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223062 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223063 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223064 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223065 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223066 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223067 (Get FASTA)   NCBI Sequence Viewer  
  XP_054223068 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC12921 (Get FASTA)   NCBI Sequence Viewer  
  AAC51759 (Get FASTA)   NCBI Sequence Viewer  
  AAF44344 (Get FASTA)   NCBI Sequence Viewer  
  AAG41406 (Get FASTA)   NCBI Sequence Viewer  
  AAG41893 (Get FASTA)   NCBI Sequence Viewer  
  AAH07533 (Get FASTA)   NCBI Sequence Viewer  
  AAH07737 (Get FASTA)   NCBI Sequence Viewer  
  AAP35641 (Get FASTA)   NCBI Sequence Viewer  
  AAP78927 (Get FASTA)   NCBI Sequence Viewer  
  AAP80144 (Get FASTA)   NCBI Sequence Viewer  
  AAQ14300 (Get FASTA)   NCBI Sequence Viewer  
  ABY87548 (Get FASTA)   NCBI Sequence Viewer  
  BAD92878 (Get FASTA)   NCBI Sequence Viewer  
  BAF85511 (Get FASTA)   NCBI Sequence Viewer  
  CAD91133 (Get FASTA)   NCBI Sequence Viewer  
  CAH10373 (Get FASTA)   NCBI Sequence Viewer  
  CAH10397 (Get FASTA)   NCBI Sequence Viewer  
  CAH18187 (Get FASTA)   NCBI Sequence Viewer  
  CDM22288 (Get FASTA)   NCBI Sequence Viewer  
  EAW85942 (Get FASTA)   NCBI Sequence Viewer  
  EAW85943 (Get FASTA)   NCBI Sequence Viewer  
  EAW85944 (Get FASTA)   NCBI Sequence Viewer  
  EAW85945 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000265371.3
  ENSP00000363949.3
  ENSP00000363954
  ENSP00000363954.5
  ENSP00000363955
  ENSP00000363955.4
  ENSP00000363956.5
  ENSP00000364001
  ENSP00000364001.2
  ENSP00000364009.1
  ENSP00000379317
  ENSP00000379317.1
  ENSP00000390447.1
  ENSP00000390567.1
  ENSP00000393071.1
  ENSP00000408911.2
  ENSP00000416147.1
  ENSP00000476896.1
GenBank Protein O14786 (Get FASTA)   NCBI Sequence Viewer  
  QUP61929 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_003864   ⟸   NM_003873
- Peptide Label: isoform a precursor
- UniProtKB: Q96I90 (UniProtKB/Swiss-Prot),   Q86T59 (UniProtKB/Swiss-Prot),   Q5T7F3 (UniProtKB/Swiss-Prot),   Q5T7F2 (UniProtKB/Swiss-Prot),   Q5T7F1 (UniProtKB/Swiss-Prot),   O60461 (UniProtKB/Swiss-Prot),   O14786 (UniProtKB/Swiss-Prot),   B0LPG9 (UniProtKB/Swiss-Prot),   Q96IH5 (UniProtKB/Swiss-Prot),   Q68DN3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001019800   ⟸   NM_001024629
- Peptide Label: isoform c precursor
- UniProtKB: E7EX60 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001019799   ⟸   NM_001024628
- Peptide Label: isoform b precursor
- UniProtKB: Q5T7F0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001231902   ⟸   NM_001244973
- Peptide Label: isoform e precursor
- UniProtKB: A8K9V7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001231901   ⟸   NM_001244972
- Peptide Label: isoform d precursor
- UniProtKB: A8K9V7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006717588   ⟸   XM_006717525
- Peptide Label: isoform X6
- UniProtKB: A8K9V7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006717587   ⟸   XM_006717524
- Peptide Label: isoform X5
- UniProtKB: A8K9V7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006717585   ⟸   XM_006717522
- Peptide Label: isoform X2
- UniProtKB: Q6X907 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006717584   ⟸   XM_006717521
- Peptide Label: isoform X1
- UniProtKB: Q68DN3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006717589   ⟸   XM_006717526
- Peptide Label: isoform X8
- UniProtKB: Q5T7F0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518058   ⟸   XM_011519756
- Peptide Label: isoform X10
- UniProtKB: E7EX60 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518057   ⟸   XM_011519755
- Peptide Label: isoform X9
- UniProtKB: Q5T7F0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016872354   ⟸   XM_017016865
- Peptide Label: isoform X4
- UniProtKB: Q6X907 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001316997   ⟸   NM_001330068
- Peptide Label: isoform f precursor
- UniProtKB: E9PEP6 (UniProtKB/TrEMBL),   Q6X907 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000476896   ⟸   ENST00000466932
RefSeq Acc Id: ENSP00000364001   ⟸   ENST00000374867
RefSeq Acc Id: ENSP00000364009   ⟸   ENST00000374875
RefSeq Acc Id: ENSP00000363949   ⟸   ENST00000374816
RefSeq Acc Id: ENSP00000363955   ⟸   ENST00000374822
RefSeq Acc Id: ENSP00000363956   ⟸   ENST00000374823
RefSeq Acc Id: ENSP00000363954   ⟸   ENST00000374821
RefSeq Acc Id: ENSP00000390447   ⟸   ENST00000413802
RefSeq Acc Id: ENSP00000390567   ⟸   ENST00000455749
RefSeq Acc Id: ENSP00000416147   ⟸   ENST00000418675
RefSeq Acc Id: ENSP00000393071   ⟸   ENST00000431894
RefSeq Acc Id: ENSP00000408911   ⟸   ENST00000432372
RefSeq Acc Id: ENSP00000379317   ⟸   ENST00000395995
RefSeq Acc Id: ENSP00000265371   ⟸   ENST00000265371
RefSeq Acc Id: XP_047281933   ⟸   XM_047425977
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047281932   ⟸   XM_047425976
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047281934   ⟸   XM_047425978
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054223053   ⟸   XM_054367078
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054223048   ⟸   XM_054367073
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054223051   ⟸   XM_054367076
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054223056   ⟸   XM_054367081
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054223052   ⟸   XM_054367077
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054223047   ⟸   XM_054367072
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054223064   ⟸   XM_054367089
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054223058   ⟸   XM_054367083
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054223049   ⟸   XM_054367074
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054223062   ⟸   XM_054367087
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054223057   ⟸   XM_054367082
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054223050   ⟸   XM_054367075
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054223046   ⟸   XM_054367071
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054223063   ⟸   XM_054367088
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054223061   ⟸   XM_054367086
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054223055   ⟸   XM_054367080
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054223054   ⟸   XM_054367079
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054223045   ⟸   XM_054367070
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054223065   ⟸   XM_054367090
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054223060   ⟸   XM_054367085
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054223059   ⟸   XM_054367084
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054223067   ⟸   XM_054367092
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054223066   ⟸   XM_054367091
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054223068   ⟸   XM_054367093
- Peptide Label: isoform X10
Protein Domains
CUB   F5/8 type C   MAM   Neuropilin C-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O14786-F1-model_v2 AlphaFold O14786 1-923 view protein structure

Promoters
RGD ID:7217329
Promoter ID:EPDNEW_H14410
Type:initiation region
Name:NRP1_2
Description:neuropilin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H14411  EPDNEW_H14412  EPDNEW_H14413  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,334,321 - 33,334,381EPDNEW
RGD ID:7217331
Promoter ID:EPDNEW_H14411
Type:initiation region
Name:NRP1_1
Description:neuropilin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H14410  EPDNEW_H14412  EPDNEW_H14413  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,334,667 - 33,334,727EPDNEW
RGD ID:7217333
Promoter ID:EPDNEW_H14412
Type:initiation region
Name:NRP1_3
Description:neuropilin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H14410  EPDNEW_H14411  EPDNEW_H14413  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,334,866 - 33,334,926EPDNEW
RGD ID:7217335
Promoter ID:EPDNEW_H14413
Type:initiation region
Name:NRP1_4
Description:neuropilin 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H14410  EPDNEW_H14411  EPDNEW_H14412  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381033,335,113 - 33,335,173EPDNEW
RGD ID:6787934
Promoter ID:HG_KWN:9109
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell
Transcripts:OTTHUMT00000051213
Position:
Human AssemblyChrPosition (strand)Source
Build 361033,593,126 - 33,593,626 (-)MPROMDB
RGD ID:6787551
Promoter ID:HG_KWN:9112
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3
Transcripts:ENST00000374814,   ENST00000374816,   ENST00000374823,   ENST00000374828,   ENST00000374833,   NM_001024628,   NM_001024629,   NM_003873,   UC001IWV.2,   UC001IWW.2,   UC001IWY.2,   UC001IXB.1,   UC001IXC.1,   UC009XLZ.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361033,663,421 - 33,664,952 (-)MPROMDB
RGD ID:6851584
Promoter ID:EP73594
Type:initiation region
Name:HS_NRP1
Description:Neuropilin 1.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:NEDO full length human cDNA sequencing project.; Oligo-capping
Position:
Human AssemblyChrPosition (strand)Source
Build 361033,663,505 - 33,663,565EPD
RGD ID:6787547
Promoter ID:HG_KWN:9113
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:ENST00000265371
Position:
Human AssemblyChrPosition (strand)Source
Build 361033,664,921 - 33,665,421 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8004 AgrOrtholog
COSMIC NRP1 COSMIC
Ensembl Genes ENSG00000099250 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000265371.8 UniProtKB/Swiss-Prot
  ENST00000374816.7 UniProtKB/TrEMBL
  ENST00000374821 ENTREZGENE
  ENST00000374821.9 UniProtKB/Swiss-Prot
  ENST00000374822 ENTREZGENE
  ENST00000374822.8 UniProtKB/Swiss-Prot
  ENST00000374823.9 UniProtKB/TrEMBL
  ENST00000374867 ENTREZGENE
  ENST00000374867.7 UniProtKB/Swiss-Prot
  ENST00000374875 ENTREZGENE
  ENST00000374875.5 UniProtKB/TrEMBL
  ENST00000395995 ENTREZGENE
  ENST00000395995.5 UniProtKB/TrEMBL
  ENST00000413802.1 UniProtKB/TrEMBL
  ENST00000418675.5 UniProtKB/TrEMBL
  ENST00000431894.5 UniProtKB/TrEMBL
  ENST00000432372.6 UniProtKB/TrEMBL
  ENST00000455749.1 UniProtKB/TrEMBL
  ENST00000466932.1 UniProtKB/TrEMBL
Gene3D-CATH 2.60.120.200 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.60.120.290 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Galactose-binding domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000099250 GTEx
HGNC ID HGNC:8004 ENTREZGENE
Human Proteome Map NRP1 Human Proteome Map
InterPro ConA-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CUB_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FA58C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Galactose-bd-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MAM_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Neuropilin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Neuropilin_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sperma_CUB_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:8829 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 8829 ENTREZGENE
OMIM 602069 OMIM
PANTHER APICAL ENDOSOMAL GLYCOPROTEIN PRECURSOR UniProtKB/TrEMBL
  F5/8 TYPE C DOMAIN-CONTAINING PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR46806:SF4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RT07201P-RELATED UniProtKB/TrEMBL
Pfam CUB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DUF3481 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  F5_F8_type_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MAM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA31783 PharmGKB
PIRSF Neuropilin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PRINTS MAMDOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE CUB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FA58C_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FA58C_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FA58C_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MAM_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MAM_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART CUB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FA58C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MAM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF49785 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF49854 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF49899 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8K9V7 ENTREZGENE, UniProtKB/TrEMBL
  B0LPG9 ENTREZGENE
  E7EX60 ENTREZGENE, UniProtKB/TrEMBL
  E9PEP6 ENTREZGENE, UniProtKB/TrEMBL
  H0Y4A0_HUMAN UniProtKB/TrEMBL
  H0Y4N6_HUMAN UniProtKB/TrEMBL
  H0Y7Z2_HUMAN UniProtKB/TrEMBL
  NRP1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  O60461 ENTREZGENE
  Q59F20_HUMAN UniProtKB/TrEMBL
  Q5JWQ2_HUMAN UniProtKB/TrEMBL
  Q5JWQ4_HUMAN UniProtKB/TrEMBL
  Q5JWQ6_HUMAN UniProtKB/TrEMBL
  Q5T7F0 ENTREZGENE, UniProtKB/TrEMBL
  Q5T7F1 ENTREZGENE
  Q5T7F2 ENTREZGENE
  Q5T7F3 ENTREZGENE
  Q68DN3 ENTREZGENE, UniProtKB/TrEMBL
  Q6AWA9_HUMAN UniProtKB/TrEMBL
  Q6X907 ENTREZGENE, UniProtKB/TrEMBL
  Q71SW6_HUMAN UniProtKB/TrEMBL
  Q7Z5M2_HUMAN UniProtKB/TrEMBL
  Q86T59 ENTREZGENE
  Q96I90 ENTREZGENE
  Q96IH5 ENTREZGENE
  Q9H2D7_HUMAN UniProtKB/TrEMBL
  Q9H2D8_HUMAN UniProtKB/TrEMBL
  Q9H2D9_HUMAN UniProtKB/TrEMBL
  Q9H2E0_HUMAN UniProtKB/TrEMBL
  Q9H2E1_HUMAN UniProtKB/TrEMBL
  V9GYL7_HUMAN UniProtKB/TrEMBL
UniProt Secondary B0LPG9 UniProtKB/Swiss-Prot
  O60461 UniProtKB/Swiss-Prot
  Q5T7F1 UniProtKB/Swiss-Prot
  Q5T7F2 UniProtKB/Swiss-Prot
  Q5T7F3 UniProtKB/Swiss-Prot
  Q86T59 UniProtKB/Swiss-Prot
  Q96I90 UniProtKB/Swiss-Prot
  Q96IH5 UniProtKB/Swiss-Prot