VASP (vasodilator stimulated phosphoprotein) - Rat Genome Database

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Gene: VASP (vasodilator stimulated phosphoprotein) Homo sapiens
Analyze
Symbol: VASP
Name: vasodilator stimulated phosphoprotein
RGD ID: 1323055
HGNC Page HGNC:12652
Description: Enables profilin binding activity. Involved in positive regulation of actin filament polymerization. Located in cytosol; focal adhesion; and plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: vasodilator-stimulated phosphoprotein
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
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381945,507,479 - 45,526,983 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1945,506,579 - 45,526,989 (+)EnsemblGRCh38hg38GRCh38
GRCh371946,010,737 - 46,030,241 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361950,702,528 - 50,722,081 (+)NCBINCBI36Build 36hg18NCBI36
Build 341950,702,527 - 50,722,078NCBI
Celera1942,816,794 - 42,836,352 (+)NCBICelera
Cytogenetic Map19q13.32NCBI
HuRef1942,440,143 - 42,459,463 (+)NCBIHuRef
CHM1_11946,013,932 - 46,033,484 (+)NCBICHM1_1
T2T-CHM13v2.01948,334,741 - 48,354,257 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,1-dichloroethene  (ISO)
1,2-dimethylhydrazine  (ISO)
1-naphthyl isothiocyanate  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (ISO)
17beta-hydroxy-5alpha-androstan-3-one  (EXP)
1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4,6-tribromophenol  (EXP)
3,3',5,5'-tetrabromobisphenol A  (EXP)
3-chloropropane-1,2-diol  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (EXP)
4-hydroxyphenyl retinamide  (ISO)
5-fluorouracil  (ISO)
6-propyl-2-thiouracil  (ISO)
8-(4-chlorophenylthio)-cGMP  (EXP,ISO)
acetaldehyde  (ISO)
acetamide  (ISO)
ADP  (EXP)
all-trans-retinoic acid  (EXP)
amitrole  (ISO)
antirheumatic drug  (EXP)
aristolochic acid A  (EXP)
atrazine  (EXP)
benomyl  (ISO)
benzatropine  (EXP)
benzo[a]pyrene  (EXP,ISO)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (EXP,ISO)
Bisphenol B  (EXP)
bortezomib  (EXP)
Brodifacoum  (ISO)
butanal  (EXP)
cadmium atom  (EXP)
caffeine  (EXP)
cannabidiol  (EXP)
carbamazepine  (ISO)
carbon monoxide  (ISO)
carbon nanotube  (ISO)
chlorpyrifos  (ISO)
choline  (ISO)
chromium atom  (ISO)
clopidogrel  (EXP)
cobalt dichloride  (EXP)
colforsin daropate hydrochloride  (EXP,ISO)
copper(II) sulfate  (EXP)
Cuprizon  (ISO)
curcumin  (EXP)
cycloheximide  (ISO)
cyclosporin A  (EXP)
cyproconazole  (ISO)
DDE  (EXP)
dexamethasone  (EXP,ISO)
dibutyl phthalate  (ISO)
dioxygen  (ISO)
doxorubicin  (EXP,ISO)
endosulfan  (ISO)
epoxiconazole  (ISO)
ethanol  (EXP)
fipronil  (ISO)
flusilazole  (ISO)
flutamide  (ISO)
folic acid  (ISO)
genistein  (EXP)
gentamycin  (ISO)
hemin  (ISO)
indometacin  (EXP)
isoprenaline  (ISO)
ivermectin  (EXP)
L-methionine  (ISO)
lead diacetate  (ISO)
mercury atom  (ISO)
mercury(0)  (ISO)
methimazole  (ISO)
methylmercury chloride  (ISO)
microcystin-LR  (EXP)
N-[2-(4-bromocinnamylamino)ethyl]isoquinoline-5-sulfonamide  (EXP)
N-nitrosodiethylamine  (ISO)
N-nitrosodimethylamine  (ISO)
nebivolol  (ISO)
nickel atom  (EXP)
nitroglycerin  (EXP,ISO)
oxycodone  (ISO)
paracetamol  (ISO)
paraquat  (ISO)
pentachlorophenol  (ISO)
pentaerythritol tetranitrate  (ISO)
perfluorohexanesulfonic acid  (ISO)
phenobarbital  (ISO)
progesterone  (EXP)
propiconazole  (ISO)
prostaglandin E1  (EXP)
prostaglandin E2  (ISO)
resveratrol  (EXP,ISO)
S-nitroso-N-acetyl-D-penicillamine  (ISO)
SB 203580  (EXP)
SB 431542  (EXP)
silibinin  (EXP)
Silidianin  (EXP)
silychristin  (EXP)
simvastatin  (ISO)
sodium arsenite  (ISO)
Soman  (ISO)
staurosporine  (ISO)
sucrose  (ISO)
sulfadimethoxine  (ISO)
sulindac sulfone  (EXP)
sunitinib  (EXP)
tacrolimus hydrate  (EXP)
tamibarotene  (EXP)
testosterone  (ISO)
testosterone enanthate  (EXP)
tetrachloromethane  (ISO)
thimerosal  (EXP)
thioacetamide  (ISO)
tremolite asbestos  (ISO)
valproic acid  (EXP,ISO)
vancomycin  (ISO)
vinclozolin  (ISO)
vincristine  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1318192   PMID:1319722   PMID:7644520   PMID:7737110   PMID:7828592   PMID:7925440   PMID:8182057   PMID:8812448   PMID:8836115   PMID:10087267   PMID:10438535   PMID:10637295  
PMID:10747096   PMID:10801818   PMID:10851246   PMID:10882740   PMID:10892742   PMID:10922374   PMID:10990454   PMID:11093254   PMID:11313394   PMID:11598004   PMID:11756574   PMID:12087107  
PMID:12220179   PMID:12372613   PMID:12397215   PMID:12477932   PMID:12492113   PMID:12566781   PMID:12571287   PMID:12576312   PMID:12652017   PMID:12665801   PMID:12695497   PMID:12805219  
PMID:14506234   PMID:14557252   PMID:14592989   PMID:14679200   PMID:14706852   PMID:14744259   PMID:15148305   PMID:15158464   PMID:15178555   PMID:15469845   PMID:15469846   PMID:15489334  
PMID:15569942   PMID:15592455   PMID:15634270   PMID:15642358   PMID:15939738   PMID:16046415   PMID:16055720   PMID:16189514   PMID:16197368   PMID:16336193   PMID:16376568   PMID:16531412  
PMID:16631741   PMID:16940418   PMID:17082196   PMID:17167837   PMID:17351763   PMID:17412998   PMID:17488353   PMID:17599063   PMID:17684063   PMID:17914456   PMID:17938817   PMID:18029348  
PMID:18064332   PMID:18217157   PMID:18278200   PMID:18559661   PMID:18569864   PMID:18680720   PMID:18813837   PMID:18832777   PMID:18845790   PMID:18923426   PMID:19056867   PMID:19059569  
PMID:19060904   PMID:19081821   PMID:19115233   PMID:19380743   PMID:19435808   PMID:19463377   PMID:19542561   PMID:19608861   PMID:19690214   PMID:19738201   PMID:19798690   PMID:19825941  
PMID:19885626   PMID:19902490   PMID:19943879   PMID:20044140   PMID:20110575   PMID:20195357   PMID:20458337   PMID:20467437   PMID:20589315   PMID:20618440   PMID:20624010   PMID:20695985  
PMID:20802179   PMID:20822337   PMID:20826790   PMID:20945373   PMID:21041447   PMID:21158099   PMID:21163344   PMID:21398369   PMID:21423176   PMID:21423205   PMID:21451103   PMID:21702043  
PMID:21814501   PMID:21827504   PMID:21873635   PMID:21874265   PMID:21911467   PMID:22014333   PMID:22210825   PMID:22212857   PMID:22320863   PMID:22623428   PMID:22658674   PMID:22863883  
PMID:22939629   PMID:23153535   PMID:23402259   PMID:23436459   PMID:23443559   PMID:23469931   PMID:23685951   PMID:23846685   PMID:24076653   PMID:24496446   PMID:24732788   PMID:24857403  
PMID:24927568   PMID:24963131   PMID:25051011   PMID:25117404   PMID:25241761   PMID:25246528   PMID:25298072   PMID:25355952   PMID:25416956   PMID:25450970   PMID:25457586   PMID:25468996  
PMID:25543053   PMID:25759389   PMID:25814554   PMID:26186194   PMID:26295568   PMID:26336132   PMID:26344197   PMID:26496610   PMID:26576037   PMID:26611125   PMID:26673895   PMID:26760575  
PMID:26777405   PMID:26871637   PMID:27173435   PMID:27684187   PMID:27711191   PMID:28209486   PMID:28376489   PMID:28378594   PMID:28514442   PMID:28526707   PMID:28667124   PMID:29117863  
PMID:29426014   PMID:29460479   PMID:29497031   PMID:29507755   PMID:29509190   PMID:29540532   PMID:29892012   PMID:30021884   PMID:30196744   PMID:30279729   PMID:30282752   PMID:30397336  
PMID:30463566   PMID:30773093   PMID:30814249   PMID:30816548   PMID:30890647   PMID:31093978   PMID:31257464   PMID:31270029   PMID:31478661   PMID:31987909   PMID:32141559   PMID:32200035  
PMID:32296183   PMID:32397169   PMID:32460013   PMID:32470361   PMID:32687490   PMID:32780723   PMID:32997728   PMID:33184177   PMID:33845483   PMID:33961781   PMID:34079125   PMID:34299191  
PMID:34316702   PMID:35044719   PMID:35256949   PMID:35271311   PMID:35384245   PMID:35411049   PMID:35562734   PMID:35831314   PMID:35944360   PMID:36215168   PMID:36217030   PMID:36238292  
PMID:36307841   PMID:36543142   PMID:37120454   PMID:37890607  


Genomics

Comparative Map Data
VASP
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381945,507,479 - 45,526,983 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1945,506,579 - 45,526,989 (+)EnsemblGRCh38hg38GRCh38
GRCh371946,010,737 - 46,030,241 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361950,702,528 - 50,722,081 (+)NCBINCBI36Build 36hg18NCBI36
Build 341950,702,527 - 50,722,078NCBI
Celera1942,816,794 - 42,836,352 (+)NCBICelera
Cytogenetic Map19q13.32NCBI
HuRef1942,440,143 - 42,459,463 (+)NCBIHuRef
CHM1_11946,013,932 - 46,033,484 (+)NCBICHM1_1
T2T-CHM13v2.01948,334,741 - 48,354,257 (+)NCBIT2T-CHM13v2.0
Vasp
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39718,990,854 - 19,005,779 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl718,990,854 - 19,005,742 (-)EnsemblGRCm39 Ensembl
GRCm38719,256,929 - 19,271,854 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl719,256,929 - 19,271,817 (-)EnsemblGRCm38mm10GRCm38
MGSCv37719,842,278 - 19,857,203 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36718,416,239 - 18,431,669 (-)NCBIMGSCv36mm8
Celera716,669,928 - 16,684,971 (-)NCBICelera
Cytogenetic Map7A3NCBI
cM Map79.51NCBI
Vasp
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8188,038,026 - 88,053,783 (-)NCBIGRCr8
mRatBN7.2178,910,009 - 78,925,791 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl178,910,011 - 78,925,061 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx184,299,066 - 84,313,957 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0192,856,629 - 92,871,541 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0186,054,149 - 86,069,040 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0180,170,608 - 80,185,882 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl180,170,619 - 80,185,882 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0181,437,091 - 81,452,900 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4178,621,494 - 78,636,762 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1178,699,598 - 78,715,028 (-)NCBI
Celera173,372,332 - 73,387,227 (-)NCBICelera
Cytogenetic Map1q21NCBI
Vasp
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495557421,911 - 34,197 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495557421,569 - 33,705 (+)NCBIChiLan1.0ChiLan1.0
VASP
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22051,668,472 - 51,688,796 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11953,540,746 - 53,560,217 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01942,457,222 - 42,476,688 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11951,053,567 - 51,072,551 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1951,053,567 - 51,072,553 (+)Ensemblpanpan1.1panPan2
VASP
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11110,050,154 - 110,063,125 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1110,050,154 - 110,062,827 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1109,534,415 - 109,547,108 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01110,582,754 - 110,595,760 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1110,582,757 - 110,595,733 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11110,258,575 - 110,271,274 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01109,892,681 - 109,905,376 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01110,762,040 - 110,774,746 (-)NCBIUU_Cfam_GSD_1.0
LOC101973767
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934917,575,109 - 17,597,696 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367061,923,602 - 1,928,630 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049367061,923,172 - 1,945,046 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
VASP
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl651,872,812 - 51,886,724 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1651,872,810 - 51,886,729 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
VASP
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1638,954,212 - 38,974,680 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl638,954,014 - 38,975,108 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607318,575,539 - 18,596,231 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Vasp
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248327,619,134 - 7,630,943 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248327,619,211 - 7,631,576 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in VASP
22 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.32(chr19:45481858-45710518)x1 copy number loss See cases [RCV000052095] Chr19:45481858..45710518 [GRCh38]
Chr19:45985116..46213776 [GRCh37]
Chr19:50676956..50905616 [NCBI36]
Chr19:19q13.32
uncertain significance
GRCh38/hg38 19q13.32(chr19:45287256-45734078)x3 copy number gain See cases [RCV000054152] Chr19:45287256..45734078 [GRCh38]
Chr19:45790514..46237336 [GRCh37]
Chr19:50482354..50929176 [NCBI36]
Chr19:19q13.32
uncertain significance
GRCh38/hg38 19q13.32-13.33(chr19:44971420-48257402)x3 copy number gain See cases [RCV000136578] Chr19:44971420..48257402 [GRCh38]
Chr19:45474677..48760659 [GRCh37]
Chr19:50166517..53452471 [NCBI36]
Chr19:19q13.32-13.33
pathogenic
GRCh38/hg38 19q13.32(chr19:45387389-46831000)x1 copy number loss See cases [RCV000137832] Chr19:45387389..46831000 [GRCh38]
Chr19:45890647..47334257 [GRCh37]
Chr19:50582487..52026097 [NCBI36]
Chr19:19q13.32
likely pathogenic
GRCh37/hg19 19q13.2-13.32(chr19:43013365-47241534)x1 copy number loss See cases [RCV000240182] Chr19:43013365..47241534 [GRCh37]
Chr19:19q13.2-13.32
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic|uncertain significance
NM_003370.4(VASP):c.605G>A (p.Gly202Glu) single nucleotide variant Inborn genetic diseases [RCV003308558] Chr19:45522466 [GRCh38]
Chr19:46025724 [GRCh37]
Chr19:19q13.32
uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19q13.32(chr19:45945375-46215558)x3 copy number gain not provided [RCV000684077] Chr19:45945375..46215558 [GRCh37]
Chr19:19q13.32
uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
NM_003370.4(VASP):c.910+9_910+10del microsatellite not provided [RCV000970359] Chr19:45523884..45523885 [GRCh38]
Chr19:46027142..46027143 [GRCh37]
Chr19:19q13.32
benign
NM_003370.4(VASP):c.310G>A (p.Ala104Thr) single nucleotide variant not provided [RCV000970358] Chr19:45518061 [GRCh38]
Chr19:46021319 [GRCh37]
Chr19:19q13.32
benign
GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3 copy number gain not provided [RCV001007050] Chr19:44738088..53621561 [GRCh37]
Chr19:19q13.31-13.42
pathogenic
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3 copy number gain not provided [RCV000845733] Chr19:28271106..49213832 [GRCh37]
Chr19:19q11-13.33
pathogenic
NM_003370.4(VASP):c.29G>A (p.Arg10Gln) single nucleotide variant Inborn genetic diseases [RCV003249588] Chr19:45517686 [GRCh38]
Chr19:46020944 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.726G>C (p.Glu242Asp) single nucleotide variant Inborn genetic diseases [RCV003249861] Chr19:45522723 [GRCh38]
Chr19:46025981 [GRCh37]
Chr19:19q13.32
uncertain significance
GRCh37/hg19 19q13.32-13.33(chr19:45531056-48174177)x3 copy number gain not provided [RCV001007051] Chr19:45531056..48174177 [GRCh37]
Chr19:19q13.32-13.33
uncertain significance
GRCh37/hg19 19q13.31-13.32(chr19:45074342-46133841) copy number gain not specified [RCV002052686] Chr19:45074342..46133841 [GRCh37]
Chr19:19q13.31-13.32
uncertain significance
NM_003370.4(VASP):c.473A>G (p.Asn158Ser) single nucleotide variant Inborn genetic diseases [RCV003257445] Chr19:45522212 [GRCh38]
Chr19:46025470 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.420G>T (p.Gln140His) single nucleotide variant Inborn genetic diseases [RCV002991078] Chr19:45521398 [GRCh38]
Chr19:46024656 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.551C>T (p.Pro184Leu) single nucleotide variant Inborn genetic diseases [RCV002684605] Chr19:45522412 [GRCh38]
Chr19:46025670 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.833C>T (p.Thr278Met) single nucleotide variant Inborn genetic diseases [RCV002945482] Chr19:45523655 [GRCh38]
Chr19:46026913 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.632C>T (p.Pro211Leu) single nucleotide variant Inborn genetic diseases [RCV002978270] Chr19:45522493 [GRCh38]
Chr19:46025751 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.851C>T (p.Thr284Ile) single nucleotide variant Inborn genetic diseases [RCV002854341] Chr19:45523673 [GRCh38]
Chr19:46026931 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.439G>A (p.Gly147Ser) single nucleotide variant Inborn genetic diseases [RCV002875036] Chr19:45522178 [GRCh38]
Chr19:46025436 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.404C>T (p.Pro135Leu) single nucleotide variant Inborn genetic diseases [RCV002930578] Chr19:45521382 [GRCh38]
Chr19:46024640 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.928T>C (p.Trp310Arg) single nucleotide variant Inborn genetic diseases [RCV002917038] Chr19:45524114 [GRCh38]
Chr19:46027372 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.280G>C (p.Gly94Arg) single nucleotide variant Inborn genetic diseases [RCV002878062] Chr19:45518031 [GRCh38]
Chr19:46021289 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.650G>C (p.Gly217Ala) single nucleotide variant Inborn genetic diseases [RCV003010888] Chr19:45522511 [GRCh38]
Chr19:46025769 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.551C>A (p.Pro184Gln) single nucleotide variant Inborn genetic diseases [RCV002963807] Chr19:45522412 [GRCh38]
Chr19:46025670 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.1050G>T (p.Glu350Asp) single nucleotide variant Inborn genetic diseases [RCV002793154] Chr19:45525948 [GRCh38]
Chr19:46029206 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.383C>G (p.Ser128Trp) single nucleotide variant Inborn genetic diseases [RCV002680480] Chr19:45521361 [GRCh38]
Chr19:46024619 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.914C>G (p.Ser305Cys) single nucleotide variant Inborn genetic diseases [RCV003214340] Chr19:45524100 [GRCh38]
Chr19:46027358 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.488C>T (p.Pro163Leu) single nucleotide variant Inborn genetic diseases [RCV003265650] Chr19:45522349 [GRCh38]
Chr19:46025607 [GRCh37]
Chr19:19q13.32
uncertain significance
NM_003370.4(VASP):c.403C>G (p.Pro135Ala) single nucleotide variant Inborn genetic diseases [RCV003361900] Chr19:45521381 [GRCh38]
Chr19:46024639 [GRCh37]
Chr19:19q13.32
uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR610hsa-miR-610Mirtarbaseexternal_infoLuciferase reporter assay//Western blotFunctional MTI22189055
MIR610hsa-miR-610OncomiRDBexternal_infoNANA22189055
MIR193Bhsa-miR-193b-3pTarbaseexternal_infoProteomicsPOSITIVE

Predicted Target Of
Summary Value
Count of predictions:4157
Count of miRNA genes:987
Interacting mature miRNAs:1246
Transcripts:ENST00000245932, ENST00000586014, ENST00000586619, ENST00000587444, ENST00000588273, ENST00000588463, ENST00000588482, ENST00000589627, ENST00000590459, ENST00000590603, ENST00000592139
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
D19S1038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371946,029,889 - 46,030,231UniSTSGRCh37
Build 361950,721,729 - 50,722,071RGDNCBI36
Celera1942,836,000 - 42,836,342RGD
Cytogenetic Map19q13.32UniSTS
VASP_8715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371946,029,502 - 46,030,258UniSTSGRCh37
Build 361950,721,342 - 50,722,098RGDNCBI36
Celera1942,835,613 - 42,836,369RGD
UniSTS:235612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371946,020,918 - 46,021,003UniSTSGRCh37
Build 361950,712,758 - 50,712,843RGDNCBI36
Celera1942,827,028 - 42,827,113RGD
HuRef1942,450,402 - 42,450,487UniSTS


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 33 33
Medium 2439 2908 1676 575 1914 416 3778 1566 1736 409 1460 1612 174 1 1204 2209 6 2
Low 50 50 49 4 49 579 631 1998 10 1 1 579
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_003370 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005259199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005259200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054321941 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054321942 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054321943 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC006117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK314812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL556269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC026019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC038224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG751094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG825983 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ451671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178383 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X98476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X98533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X98534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z46389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000245932   ⟹   ENSP00000245932
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,507,479 - 45,526,983 (+)Ensembl
RefSeq Acc Id: ENST00000586014   ⟹   ENSP00000467005
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,507,506 - 45,526,942 (+)Ensembl
RefSeq Acc Id: ENST00000586619
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,507,510 - 45,522,217 (+)Ensembl
RefSeq Acc Id: ENST00000587444
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,525,794 - 45,526,169 (+)Ensembl
RefSeq Acc Id: ENST00000588273
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,524,037 - 45,526,202 (+)Ensembl
RefSeq Acc Id: ENST00000588463
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,522,789 - 45,524,413 (+)Ensembl
RefSeq Acc Id: ENST00000588482   ⟹   ENSP00000466319
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,522,556 - 45,526,332 (+)Ensembl
RefSeq Acc Id: ENST00000589627   ⟹   ENSP00000467061
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,506,579 - 45,517,834 (+)Ensembl
RefSeq Acc Id: ENST00000590459
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,522,734 - 45,523,963 (+)Ensembl
RefSeq Acc Id: ENST00000590603   ⟹   ENSP00000467773
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,507,491 - 45,522,391 (+)Ensembl
RefSeq Acc Id: ENST00000592139   ⟹   ENSP00000464742
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,507,488 - 45,522,581 (+)Ensembl
RefSeq Acc Id: ENST00000705986   ⟹   ENSP00000516196
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,517,929 - 45,526,983 (+)Ensembl
RefSeq Acc Id: ENST00000705987   ⟹   ENSP00000516197
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1945,522,532 - 45,526,989 (+)Ensembl
RefSeq Acc Id: NM_003370   ⟹   NP_003361
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381945,507,479 - 45,526,983 (+)NCBI
GRCh371946,010,688 - 46,030,247 (+)NCBI
Build 361950,702,528 - 50,722,081 (+)NCBI Archive
HuRef1942,440,143 - 42,459,463 (+)ENTREZGENE
CHM1_11946,013,932 - 46,033,484 (+)NCBI
T2T-CHM13v2.01948,334,741 - 48,354,257 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005259199   ⟹   XP_005259256
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381945,507,479 - 45,526,983 (+)NCBI
GRCh371946,010,688 - 46,030,247 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005259200   ⟹   XP_005259257
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381945,507,479 - 45,526,983 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017027200   ⟹   XP_016882689
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381945,507,479 - 45,526,983 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054321941   ⟹   XP_054177916
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01948,334,741 - 48,354,257 (+)NCBI
RefSeq Acc Id: XM_054321942   ⟹   XP_054177917
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01948,334,741 - 48,354,257 (+)NCBI
RefSeq Acc Id: XM_054321943   ⟹   XP_054177918
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01948,334,741 - 48,354,257 (+)NCBI
Protein Sequences
Protein RefSeqs NP_003361 (Get FASTA)   NCBI Sequence Viewer  
  XP_005259256 (Get FASTA)   NCBI Sequence Viewer  
  XP_005259257 (Get FASTA)   NCBI Sequence Viewer  
  XP_016882689 (Get FASTA)   NCBI Sequence Viewer  
  XP_054177916 (Get FASTA)   NCBI Sequence Viewer  
  XP_054177917 (Get FASTA)   NCBI Sequence Viewer  
  XP_054177918 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH26019 (Get FASTA)   NCBI Sequence Viewer  
  AAH38224 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33839 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33840 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33841 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33842 (Get FASTA)   NCBI Sequence Viewer  
  ALQ33843 (Get FASTA)   NCBI Sequence Viewer  
  BAG37336 (Get FASTA)   NCBI Sequence Viewer  
  CAA67109 (Get FASTA)   NCBI Sequence Viewer  
  CAA67147 (Get FASTA)   NCBI Sequence Viewer  
  CAA86523 (Get FASTA)   NCBI Sequence Viewer  
  EAW57362 (Get FASTA)   NCBI Sequence Viewer  
  EAW57363 (Get FASTA)   NCBI Sequence Viewer  
  EAW57364 (Get FASTA)   NCBI Sequence Viewer  
  EAW57365 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000245932
  ENSP00000245932.5
  ENSP00000464742.1
  ENSP00000466319.1
  ENSP00000467005.1
  ENSP00000467061.1
  ENSP00000467773.1
  ENSP00000516196
  ENSP00000516196.1
  ENSP00000516197.1
GenBank Protein P50552 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_003361   ⟸   NM_003370
- UniProtKB: Q93035 (UniProtKB/Swiss-Prot),   P50552 (UniProtKB/Swiss-Prot),   Q6PIZ1 (UniProtKB/Swiss-Prot),   B2RBT9 (UniProtKB/Swiss-Prot),   A0A024R0V4 (UniProtKB/TrEMBL),   A0A0S2Z4I9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005259257   ⟸   XM_005259200
- Peptide Label: isoform X2
- UniProtKB: A0A0S2Z4I9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005259256   ⟸   XM_005259199
- Peptide Label: isoform X1
- UniProtKB: A0A0S2Z4I9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016882689   ⟸   XM_017027200
- Peptide Label: isoform X3
- UniProtKB: A0A0S2Z4I9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000467005   ⟸   ENST00000586014
RefSeq Acc Id: ENSP00000466319   ⟸   ENST00000588482
RefSeq Acc Id: ENSP00000245932   ⟸   ENST00000245932
RefSeq Acc Id: ENSP00000467061   ⟸   ENST00000589627
RefSeq Acc Id: ENSP00000467773   ⟸   ENST00000590603
RefSeq Acc Id: ENSP00000464742   ⟸   ENST00000592139
RefSeq Acc Id: ENSP00000516197   ⟸   ENST00000705987
RefSeq Acc Id: ENSP00000516196   ⟸   ENST00000705986
RefSeq Acc Id: XP_054177917   ⟸   XM_054321942
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054177916   ⟸   XM_054321941
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054177918   ⟸   XM_054321943
- Peptide Label: isoform X3
Protein Domains
VASP tetramerisation   WH1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P50552-F1-model_v2 AlphaFold P50552 1-380 view protein structure

Promoters
RGD ID:7240433
Promoter ID:EPDNEW_H25962
Type:initiation region
Name:VASP_1
Description:vasodilator-stimulated phosphoprotein
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381945,507,487 - 45,507,547EPDNEW
RGD ID:6796234
Promoter ID:HG_KWN:30285
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000377786,   NM_003370,   UC010EKI.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361950,701,701 - 50,702,692 (+)MPROMDB
RGD ID:6851596
Promoter ID:EP73600
Type:initiation region
Name:HS_VASP
Description:Vasodilator-stimulated phosphoprotein.
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 361950,702,597 - 50,702,657EPD

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:12652 AgrOrtholog
COSMIC VASP COSMIC
Ensembl Genes ENSG00000125753 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000245932 ENTREZGENE
  ENST00000245932.11 UniProtKB/Swiss-Prot
  ENST00000586014.5 UniProtKB/TrEMBL
  ENST00000588482.5 UniProtKB/TrEMBL
  ENST00000589627.1 UniProtKB/TrEMBL
  ENST00000590603.1 UniProtKB/TrEMBL
  ENST00000592139.1 UniProtKB/TrEMBL
  ENST00000705986 ENTREZGENE
  ENST00000705986.1 UniProtKB/TrEMBL
  ENST00000705987.1 UniProtKB/TrEMBL
Gene3D-CATH 2.30.29.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Vasodilator-stimulated phosphoprotein UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000125753 GTEx
HGNC ID HGNC:12652 ENTREZGENE
Human Proteome Map VASP Human Proteome Map
InterPro PH-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VASP/EVL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VASP_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  VASP_tetra UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WH1/EVH1_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:7408 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 7408 ENTREZGENE
OMIM 601703 OMIM
PANTHER PTHR11202:SF12 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SPROUTY-RELATED, EVH1 DOMAIN-CONTAINING PROTEIN FAMILY MEMBER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam VASP_tetra UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WH1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37276 PharmGKB
PIRSF Vasodilator_Phospo UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE WH1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART WH1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP PH domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF118370 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R0V4 ENTREZGENE, UniProtKB/TrEMBL
  A0A0S2Z4H6_HUMAN UniProtKB/TrEMBL
  A0A0S2Z4I7_HUMAN UniProtKB/TrEMBL
  A0A0S2Z4I9 ENTREZGENE, UniProtKB/TrEMBL
  A0A0S2Z4N8_HUMAN UniProtKB/TrEMBL
  A0A994J508_HUMAN UniProtKB/TrEMBL
  A0A994J7X3_HUMAN UniProtKB/TrEMBL
  B2RBT9 ENTREZGENE
  K7EIG8_HUMAN UniProtKB/TrEMBL
  K7EM16_HUMAN UniProtKB/TrEMBL
  K7ENL7_HUMAN UniProtKB/TrEMBL
  K7ENR7_HUMAN UniProtKB/TrEMBL
  K7EQD0_HUMAN UniProtKB/TrEMBL
  P50552 ENTREZGENE
  Q6PIZ1 ENTREZGENE
  Q93035 ENTREZGENE
  VASP_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B2RBT9 UniProtKB/Swiss-Prot
  Q6PIZ1 UniProtKB/Swiss-Prot
  Q93035 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-06-20 VASP  vasodilator stimulated phosphoprotein  VASP  vasodilator-stimulated phosphoprotein  Symbol and/or name change 5135510 APPROVED