PVT1 (Pvt1 oncogene) - Rat Genome Database

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Gene: PVT1 (Pvt1 oncogene) Homo sapiens
Analyze
Symbol: PVT1
Name: Pvt1 oncogene
RGD ID: 1348372
HGNC Page HGNC
Description: Predicted to be involved in response to wounding.
Type: ncrna
RefSeq Status: REVIEWED
Also known as: LINC00079; MGC21751; MIR1204HG; MYC; NCRNA00079; onco-lncRNA-100; Pvt1 oncogene (non-protein coding)
RGD Orthologs
Mouse
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
GRCh38.p13 Ensembl8127,794,526 - 128,187,101 (+)EnsemblGRCh38hg38GRCh38
GRCh388127,794,533 - 128,101,253 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh378128,806,779 - 129,113,499 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 368128,875,961 - 129,182,681 (+)NCBINCBI36hg18NCBI36
Celera8124,987,142 - 125,293,818 (+)NCBI
Cytogenetic Map8q24.21NCBI
HuRef8124,224,893 - 124,436,191 (+)NCBIHuRef
CHM1_18128,847,026 - 129,153,800 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

References

Additional References at PubMed
PMID:2181290   PMID:2470097   PMID:2725491   PMID:3024964   PMID:12477932   PMID:14702039   PMID:16341674   PMID:17395743   PMID:17503467   PMID:17881614   PMID:17908964   PMID:19270707  
PMID:19549893   PMID:20694011   PMID:21037568   PMID:21316338   PMID:21526116   PMID:21814516   PMID:21833088   PMID:22110125   PMID:22869583   PMID:23547836   PMID:23801869   PMID:23817571  
PMID:23934736   PMID:24132900   PMID:24196785   PMID:24204837   PMID:24220699   PMID:24390342   PMID:24529757   PMID:24709693   PMID:24780616   PMID:24821155   PMID:24861552   PMID:24926545  
PMID:25043044   PMID:25043274   PMID:25086665   PMID:25245984   PMID:25261932   PMID:25279986   PMID:25400777   PMID:25624916   PMID:25864709   PMID:25883951   PMID:25890171   PMID:25956062  
PMID:26097562   PMID:26427660   PMID:26490983   PMID:26517688   PMID:26545364   PMID:26850852   PMID:26908628   PMID:26925791   PMID:27028998   PMID:27232880   PMID:27272214   PMID:27366943  
PMID:27484035   PMID:27588491   PMID:27756785   PMID:27794184   PMID:27813492   PMID:27928058   PMID:27986464   PMID:28187158   PMID:28235236   PMID:28258379   PMID:28265576   PMID:28276314  
PMID:28296507   PMID:28351322   PMID:28381186   PMID:28404954   PMID:28409552   PMID:28520497   PMID:28534994   PMID:28602700   PMID:28611215   PMID:28656879   PMID:28657147   PMID:28731781  
PMID:28800314   PMID:28848163   PMID:28866116   PMID:28874676   PMID:28882595   PMID:28972861   PMID:29035442   PMID:29046366   PMID:29050519   PMID:29081406   PMID:29115513   PMID:29117863  
PMID:29193797   PMID:29244840   PMID:29262850   PMID:29277611   PMID:29280051   PMID:29286144   PMID:29417297   PMID:29445147   PMID:29452232   PMID:29467491   PMID:29501773   PMID:29505758  
PMID:29510227   PMID:29512788   PMID:29552759   PMID:29620147   PMID:29693171   PMID:29693417   PMID:29706652   PMID:29715456   PMID:29731168   PMID:29739059   PMID:29749550   PMID:29760406  
PMID:29803929   PMID:29845201   PMID:29948619   PMID:29957467   PMID:29975928   PMID:30001707   PMID:30076414   PMID:30076714   PMID:30083911   PMID:30141114   PMID:30205391   PMID:30222365  
PMID:30252166   PMID:30295989   PMID:30304557   PMID:30317572   PMID:30347597   PMID:30371726   PMID:30504754   PMID:30590312   PMID:30649422   PMID:30661902   PMID:30679629   PMID:30794914  
PMID:30820968   PMID:30825877   PMID:30832754   PMID:30909189   PMID:30914434   PMID:30943439   PMID:30993787   PMID:31002139   PMID:31028131   PMID:31222482   PMID:31277104   PMID:31297833  
PMID:31309249   PMID:31322217   PMID:31326971   PMID:31369196   PMID:31371698   PMID:31485648   PMID:31509024   PMID:31577719   PMID:31601234   PMID:31604907   PMID:31626590   PMID:31627090  
PMID:31677796   PMID:31696483   PMID:31699956   PMID:31707347   PMID:31755246   PMID:31850702   PMID:31877167   PMID:31894346   PMID:31957871   PMID:31986409   PMID:32003019   PMID:32196583  
PMID:32202906   PMID:32293498   PMID:32385030   PMID:32428696   PMID:32441301   PMID:32499447   PMID:32572930   PMID:32689767   PMID:32812642   PMID:32827544   PMID:32918701   PMID:32992461  
PMID:33188158   PMID:33453148   PMID:33600954  


Genomics

Comparative Map Data
PVT1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8127,794,526 - 128,187,101 (+)EnsemblGRCh38hg38GRCh38
GRCh388127,794,533 - 128,101,253 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh378128,806,779 - 129,113,499 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 368128,875,961 - 129,182,681 (+)NCBINCBI36hg18NCBI36
Celera8124,987,142 - 125,293,818 (+)NCBI
Cytogenetic Map8q24.21NCBI
HuRef8124,224,893 - 124,436,191 (+)NCBIHuRef
CHM1_18128,847,026 - 129,153,800 (+)NCBICHM1_1
Pvt1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391561,909,835 - 62,132,064 (+)NCBIGRCm39mm39
GRCm39 Ensembl1561,909,835 - 62,249,945 (+)Ensembl
GRCm381562,037,986 - 62,260,215 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1562,037,986 - 62,378,096 (+)EnsemblGRCm38mm10GRCm38
MGSCv371561,869,542 - 62,082,530 (+)NCBIGRCm37mm9NCBIm37
MGSCv361561,869,542 - 62,082,530 (+)NCBImm8
Celera1563,612,668 - 63,756,556 (+)NCBICelera
Cytogenetic Map15D1NCBI
cM Map1526.24NCBI
Pvt1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2793,656,249 - 93,879,938 (+)NCBI
Rnor_6.07102,648,394 - 102,871,316 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.07103,219,764 - 103,441,799 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera790,324,385 - 90,542,415 (+)NCBICelera
Cytogenetic Map7q33NCBI

Position Markers
D8S1720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378128,949,753 - 128,949,884UniSTSGRCh37
Build 368129,018,935 - 129,019,066RGDNCBI36
Celera8125,130,542 - 125,130,675RGD
Cytogenetic Map8q24UniSTS
HuRef8124,272,137 - 124,272,272UniSTS
Marshfield Genetic Map8140.61RGD
Marshfield Genetic Map8140.61UniSTS
Genethon Genetic Map8139.7UniSTS
deCODE Assembly Map8137.06UniSTS
Whitehead-YAC Contig Map8 UniSTS
SGC34443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378128,994,985 - 128,995,111UniSTSGRCh37
Build 368129,064,167 - 129,064,293RGDNCBI36
Celera8125,175,783 - 125,175,909RGD
Cytogenetic Map8q24UniSTS
HuRef8124,317,392 - 124,317,518UniSTS
GeneMap99-GB4 RH Map8496.14UniSTS
Whitehead-RH Map8653.1UniSTS
RH68431  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378128,995,025 - 128,995,191UniSTSGRCh37
Build 368129,064,207 - 129,064,373RGDNCBI36
Celera8125,175,823 - 125,175,989RGD
Cytogenetic Map8q24UniSTS
HuRef8124,317,432 - 124,317,598UniSTS
GeneMap99-GB4 RH Map8493.61UniSTS
SHGC-82342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378129,064,182 - 129,064,392UniSTSGRCh37
Build 368129,133,364 - 129,133,574RGDNCBI36
Celera8125,244,489 - 125,244,699RGD
Cytogenetic Map8q24UniSTS
HuRef8124,386,676 - 124,386,886UniSTS
SHGC-151203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378128,949,764 - 128,950,061UniSTSGRCh37
Build 368129,018,946 - 129,019,243RGDNCBI36
Celera8125,130,553 - 125,130,852RGD
Cytogenetic Map8q24UniSTS
HuRef8124,272,148 - 124,272,449UniSTS
TNG Radiation Hybrid Map5709.0UniSTS
TNG Radiation Hybrid Map862621.0UniSTS
SHGC-144185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378128,859,640 - 128,859,910UniSTSGRCh37
Build 368128,928,822 - 128,929,092RGDNCBI36
Celera8125,040,418 - 125,040,688RGD
Cytogenetic Map8q24UniSTS
HuRef8124,181,183 - 124,181,453UniSTS
TNG Radiation Hybrid Map862667.0UniSTS
STS-T95511  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378129,113,252 - 129,113,489UniSTSGRCh37
Build 368129,182,434 - 129,182,671RGDNCBI36
Celera8125,293,571 - 125,293,808RGD
Cytogenetic Map8q24UniSTS
HuRef8124,435,944 - 124,436,181UniSTS
GeneMap99-GB4 RH Map8489.94UniSTS
G17834  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378128,986,445 - 128,986,598UniSTSGRCh37
Build 368129,055,627 - 129,055,780RGDNCBI36
Celera8125,167,244 - 125,167,397RGD
Cytogenetic Map8q24UniSTS
HuRef8124,308,853 - 124,309,006UniSTS
SHGC-152351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378128,949,805 - 128,950,106UniSTSGRCh37
GRCh378128,949,795 - 128,950,106UniSTSGRCh37
Build 368129,018,977 - 129,019,288RGDNCBI36
Celera8125,130,594 - 125,130,897UniSTS
Celera8125,130,584 - 125,130,897RGD
Cytogenetic Map8q24UniSTS
HuRef8124,272,179 - 124,272,494UniSTS
HuRef8124,272,189 - 124,272,494UniSTS
TNG Radiation Hybrid Map1714915.0UniSTS
G31084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378129,008,730 - 129,008,861UniSTSGRCh37
Build 368129,077,912 - 129,078,043RGDNCBI36
Celera8125,189,528 - 125,189,659RGD
Cytogenetic Map8q24UniSTS
HuRef8124,331,128 - 124,331,259UniSTS
AFMB299YE9  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378129,055,938 - 129,056,144UniSTSGRCh37
Build 368129,125,120 - 129,125,326RGDNCBI36
Celera8125,236,246 - 125,236,452RGD
Cytogenetic Map8q24UniSTS
HuRef1161,164,280 - 61,165,111UniSTS
HuRef8124,378,435 - 124,378,639UniSTS
Whitehead-YAC Contig Map8 UniSTS
D8S1087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378128,957,099 - 128,957,406UniSTSGRCh37
Build 368129,026,281 - 129,026,588RGDNCBI36
Celera8125,137,891 - 125,138,198RGD
Cytogenetic Map8q24UniSTS
HuRef8124,279,488 - 124,279,795UniSTS
Whitehead-YAC Contig Map8 UniSTS
L17705  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11q12UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21.3UniSTS
D11S2977  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3q29UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic MapXp11.3UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4054
Count of miRNA genes:1001
Interacting mature miRNAs:1244
Transcripts:ENST00000504719, ENST00000512617, ENST00000513868, ENST00000517525, ENST00000517790, ENST00000517838, ENST00000518528, ENST00000519481, ENST00000520913, ENST00000521122, ENST00000521600, ENST00000521951, ENST00000522414, ENST00000522875, ENST00000522963, ENST00000523068, ENST00000523190, ENST00000523328, ENST00000523427, ENST00000524165
Prediction methods:Microtar, Miranda, Rnahybrid
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.


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 adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 104 7 41 18 655 21 71 42 25 62 271 151 4 12 4
Low 2192 2046 1356 363 1224 201 3822 1406 1347 223 1182 1441 168 1173 2335 5 1
Below cutoff 139 932 327 242 71 243 463 743 2327 130 3 17 1 19 449

Sequence

Nucleotide Sequences
RefSeq Transcripts NR_003367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC026248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC084123 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC103705 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC103819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128687 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129745 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY336081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC033263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC041065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM821521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX280136 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D79458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M25802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M25803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M26714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M31519 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M34428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M34431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125228 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125230 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125231 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125234 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MF125263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MG562504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MG562505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MG562506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MG562507 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MG562508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  MG562509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA989217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA989218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA989219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X04620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000504719
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,535 - 127,932,706 (+)Ensembl
RefSeq Acc Id: ENST00000512617
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,004 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000513868
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,890,628 - 128,101,253 (+)Ensembl
RefSeq Acc Id: ENST00000517525
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,538 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000517790
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,209 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000517838
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,890,587 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000518528
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,139 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000519481
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,854,398 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000520913
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,854,396 - 127,932,696 (+)Ensembl
RefSeq Acc Id: ENST00000521122
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,854,396 - 127,932,708 (+)Ensembl
RefSeq Acc Id: ENST00000521600
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,989,217 - 128,096,578 (+)Ensembl
RefSeq Acc Id: ENST00000521951
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,557 - 127,940,454 (+)Ensembl
RefSeq Acc Id: ENST00000522414
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,388 - 128,099,890 (+)Ensembl
RefSeq Acc Id: ENST00000522875
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,989,261 - 128,096,656 (+)Ensembl
RefSeq Acc Id: ENST00000522963
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,221 - 127,932,720 (+)Ensembl
RefSeq Acc Id: ENST00000523068
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,796,033 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000523190
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,009,614 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000523328
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,565 - 127,932,709 (+)Ensembl
RefSeq Acc Id: ENST00000523427
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,567 - 127,891,257 (+)Ensembl
RefSeq Acc Id: ENST00000524165
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,557 - 127,932,710 (+)Ensembl
RefSeq Acc Id: ENST00000612011
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,939,508 - 127,939,676 (+)Ensembl
RefSeq Acc Id: ENST00000613916
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,096,518 - 128,096,654 (+)Ensembl
RefSeq Acc Id: ENST00000615125
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,541 - 127,794,734 (+)Ensembl
RefSeq Acc Id: ENST00000615442
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,855,155 - 127,855,319 (+)Ensembl
RefSeq Acc Id: ENST00000616386
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,070,160 - 128,070,272 (+)Ensembl
RefSeq Acc Id: ENST00000617087
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,989,162 - 127,989,291 (+)Ensembl
RefSeq Acc Id: ENST00000650846
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,120,269 - 128,187,031 (+)Ensembl
RefSeq Acc Id: ENST00000650930
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,230 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000651568
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,854,400 - 127,932,712 (+)Ensembl
RefSeq Acc Id: ENST00000651587
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,541 - 128,187,101 (+)Ensembl
RefSeq Acc Id: ENST00000651664
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,890,226 - 127,932,712 (+)Ensembl
RefSeq Acc Id: ENST00000652492
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,027,509 - 128,101,099 (+)Ensembl
RefSeq Acc Id: ENST00000652695
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,859,787 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000652728
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,351 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000652816
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,537 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000652883
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,233 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000652993
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,046,371 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000653406
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,891,959 - 127,932,708 (+)Ensembl
RefSeq Acc Id: ENST00000653497
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,994,949 - 128,101,254 (+)Ensembl
RefSeq Acc Id: ENST00000653522
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,527 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000653608
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,367 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000653845
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,538 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000653853
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,008,879 - 128,101,252 (+)Ensembl
RefSeq Acc Id: ENST00000653990
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,983,878 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000654091
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,565 - 127,999,334 (+)Ensembl
RefSeq Acc Id: ENST00000654105
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,683 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000654324
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,550 - 128,101,252 (+)Ensembl
RefSeq Acc Id: ENST00000654369
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,346 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000655099
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,004 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000655148
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,409 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000655594
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,846,054 - 127,852,712 (+)Ensembl
RefSeq Acc Id: ENST00000655783
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,000 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000656077
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,046,604 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000656168
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,409 - 127,820,382 (+)Ensembl
RefSeq Acc Id: ENST00000656396
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,967 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000656402
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,590 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000656411
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,004 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000656491
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,609 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000656532
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,358 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000656693
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,802 - 127,990,365 (+)Ensembl
RefSeq Acc Id: ENST00000656880
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,537 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000656948
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,854,709 - 127,932,706 (+)Ensembl
RefSeq Acc Id: ENST00000656999
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,998,029 - 128,101,255 (+)Ensembl
RefSeq Acc Id: ENST00000657112
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,559 - 128,083,366 (+)Ensembl
RefSeq Acc Id: ENST00000657183
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,542 - 127,932,696 (+)Ensembl
RefSeq Acc Id: ENST00000657211
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,538 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000657289
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,533 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000657297
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,559 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000657356
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,567 - 128,099,887 (+)Ensembl
RefSeq Acc Id: ENST00000657384
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,198 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000657449
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,575 - 128,101,254 (+)Ensembl
RefSeq Acc Id: ENST00000657451
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,763 - 128,101,254 (+)Ensembl
RefSeq Acc Id: ENST00000657517
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,535 - 127,852,712 (+)Ensembl
RefSeq Acc Id: ENST00000657596
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,346 - 127,932,700 (+)Ensembl
RefSeq Acc Id: ENST00000657667
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,754 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000657682
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,406 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000657693
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,555 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000657844
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,233 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000657945
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,408 - 128,099,677 (+)Ensembl
RefSeq Acc Id: ENST00000658018
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,317 - 128,101,250 (+)Ensembl
RefSeq Acc Id: ENST00000658065
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,409 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000658158
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,152 - 128,096,763 (+)Ensembl
RefSeq Acc Id: ENST00000658242
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,912,004 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000658305
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,046,599 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000658350
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,997,754 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000658429
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,039,647 - 128,101,252 (+)Ensembl
RefSeq Acc Id: ENST00000658556
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,550 - 127,932,708 (+)Ensembl
RefSeq Acc Id: ENST00000658840
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,997,045 - 127,999,334 (+)Ensembl
RefSeq Acc Id: ENST00000659106
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,997,045 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000659326
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,196 - 127,996,681 (+)Ensembl
RefSeq Acc Id: ENST00000659625
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,802 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000659666
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,004 - 128,101,252 (+)Ensembl
RefSeq Acc Id: ENST00000659892
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,171 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000659912
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,820 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000660069
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,048,250 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000660122
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,004 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000660146
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,285 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000660200
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,537 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000660438
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,155 - 128,017,217 (+)Ensembl
RefSeq Acc Id: ENST00000660456
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,773 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000660631
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,565 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000660659
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,282 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000660781
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,193 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000660896
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,928 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000660912
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,204 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000661160
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,180 - 127,932,708 (+)Ensembl
RefSeq Acc Id: ENST00000661205
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,796 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000661391
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,285 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000661625
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,346 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000661830
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,533 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000661988
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,413 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000662061
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,590 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000662410
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,560 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000662413
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,565 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000662709
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,004 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000662766
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,537 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000663059
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,799 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000663461
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,890,601 - 128,101,252 (+)Ensembl
RefSeq Acc Id: ENST00000663715
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,230 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000663753
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,559 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000664139
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,531 - 127,932,708 (+)Ensembl
RefSeq Acc Id: ENST00000664214
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,527 - 127,932,707 (+)Ensembl
RefSeq Acc Id: ENST00000664265
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,563 - 128,083,335 (+)Ensembl
RefSeq Acc Id: ENST00000664293
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,559 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000664299
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,808 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000664610
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,998,216 - 128,070,873 (+)Ensembl
RefSeq Acc Id: ENST00000664742
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,004 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000664924
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,854,728 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000664995
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,353 - 128,101,247 (+)Ensembl
RefSeq Acc Id: ENST00000665166
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,854,635 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000665175
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,082,378 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000665246
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,196 - 127,932,708 (+)Ensembl
RefSeq Acc Id: ENST00000665372
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,565 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000665698
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,559 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000665721
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,700 - 127,995,300 (+)Ensembl
RefSeq Acc Id: ENST00000665737
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,559 - 128,101,254 (+)Ensembl
RefSeq Acc Id: ENST00000665856
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,538 - 127,943,442 (+)Ensembl
RefSeq Acc Id: ENST00000666039
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,046,607 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000666076
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,004 - 127,995,613 (+)Ensembl
RefSeq Acc Id: ENST00000666080
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,555 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000666105
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,409 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000666147
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,997,046 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000666223
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,409 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000666353
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,542 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000666452
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,984,004 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000666776
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,808 - 128,099,890 (+)Ensembl
RefSeq Acc Id: ENST00000666777
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,600 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000666842
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,200 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000666878
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,332 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000667149
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,932 - 127,942,997 (+)Ensembl
RefSeq Acc Id: ENST00000667204
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,600 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000667305
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,526 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000667418
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,576 - 128,071,539 (+)Ensembl
RefSeq Acc Id: ENST00000667539
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,555 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000667630
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,095,298 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000667714
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,675 - 128,101,255 (+)Ensembl
RefSeq Acc Id: ENST00000668098
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,997,045 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000668123
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,808 - 128,101,255 (+)Ensembl
RefSeq Acc Id: ENST00000668215
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,400 - 128,096,758 (+)Ensembl
RefSeq Acc Id: ENST00000668351
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,401 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000668479
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,048,135 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000668480
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,409 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000668619
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,047,339 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000669082
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,854,500 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000669132
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,537 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000669272
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,813 - 127,942,997 (+)Ensembl
RefSeq Acc Id: ENST00000669407
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,916,559 - 127,943,001 (+)Ensembl
RefSeq Acc Id: ENST00000669416
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,149 - 127,932,710 (+)Ensembl
RefSeq Acc Id: ENST00000669509
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,378 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000669951
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,561 - 127,996,667 (+)Ensembl
RefSeq Acc Id: ENST00000670009
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,400 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000670204
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,855,209 - 128,017,216 (+)Ensembl
RefSeq Acc Id: ENST00000670223
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,537 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000670532
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,926 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000670535
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,049,400 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000670602
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,890,196 - 127,932,701 (+)Ensembl
RefSeq Acc Id: ENST00000670626
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,890,715 - 127,996,670 (+)Ensembl
RefSeq Acc Id: ENST00000670714
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,795,552 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000670795
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,794,561 - 127,995,232 (+)Ensembl
RefSeq Acc Id: ENST00000671088
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,854,724 - 128,101,256 (+)Ensembl
RefSeq Acc Id: ENST00000671092
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8127,998,358 - 128,099,834 (+)Ensembl
RefSeq Acc Id: ENST00000671587
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8128,045,317 - 128,101,256 (+)Ensembl
RefSeq Acc Id: NR_003367
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388127,794,533 - 128,101,253 (+)NCBI
GRCh378128,902,874 - 129,113,499 (+)NCBI
Build 368128,875,961 - 129,182,681 (+)NCBI Archive
HuRef8124,224,893 - 124,436,191 (+)NCBI
CHM1_18128,847,026 - 129,153,800 (+)NCBI
Sequence:
Promoters
RGD ID:15096262
Promoter ID:EPDNEWNC_H1104
Type:multiple initiation site
Name:PVT1_1
Description:Pvt1 oncogene [Source:HGNC Symbol;Acc:HGNC:9709]
SO ACC ID:SO:0000170
Source:EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh388127,794,541 - 127,794,601EPDNEWNC
RGD ID:15096261
Promoter ID:EPDNEWNC_H1105
Type:initiation region
Name:PVT1_2
Description:Pvt1 oncogene [Source:HGNC Symbol;Acc:HGNC:9709]
SO ACC ID:SO:0000170
Source:EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh388127,795,813 - 127,795,873EPDNEWNC
RGD ID:6806978
Promoter ID:HG_KWN:62085
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000398994,   NR_003367,   UC003YSJ.2,   UC010MDP.1
Position:
Human AssemblyChrPosition (strand)Source
Build 368128,875,766 - 128,876,266 (+)MPROMDB
RGD ID:6813495
Promoter ID:HG_ACW:78839
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   Lymphoblastoid,   NB4
Transcripts:PVT1.RAPR07,   PVT1.SAPR07,   PVT1.TAPR07,   PVT1.VFAPR07,   PVT1.VHAPR07,   PVT1.VLAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 368128,876,496 - 128,877,382 (+)MPROMDB
RGD ID:6813497
Promoter ID:HG_ACW:78856
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:PVT1.VNAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 368129,020,786 - 129,021,287 (+)MPROMDB
RGD ID:6813493
Promoter ID:HG_ACW:78860
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid,   NB4
Transcripts:PVT1.AAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 368129,075,074 - 129,075,574 (+)MPROMDB
RGD ID:6813491
Promoter ID:HG_ACW:78867
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562,   Lymphoblastoid,   NB4
Transcripts:PVT1.BAPR07,   PVT1.KAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 368129,129,911 - 129,131,047 (+)MPROMDB
RGD ID:6813494
Promoter ID:HG_ACW:78871
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:PVT1.PAPR07-UNSPLICED
Position:
Human AssemblyChrPosition (strand)Source
Build 368129,163,601 - 129,164,101 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8q23.3-24.3(chr8:113580402-145054634)x3 copy number gain See cases [RCV000050638] Chr8:113580402..145054634 [GRCh38]
Chr8:114592631..146280020 [GRCh37]
Chr8:114661807..146250824 [NCBI36]
Chr8:8q23.3-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:95606052-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|See cases [RCV000053677] Chr8:95606052..145054775 [GRCh38]
Chr8:96618280..146280161 [GRCh37]
Chr8:96687456..146250965 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000053678] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q24.21-24.23(chr8:126626164-137169427)x1 copy number loss See cases [RCV000054306] Chr8:126626164..137169427 [GRCh38]
Chr8:127638409..138181670 [GRCh37]
Chr8:127707591..138250852 [NCBI36]
Chr8:8q24.21-24.23
pathogenic
NR_003367.2(PVT1):n.972-2158A>G single nucleotide variant Lung cancer [RCV000107027] Chr8:128068002 [GRCh38]
Chr8:129080248 [GRCh37]
Chr8:8q24.21
uncertain significance
NR_003367.2(PVT1):n.372-3935A>G single nucleotide variant Lung cancer [RCV000107024] Chr8:127935573 [GRCh38]
Chr8:128947819 [GRCh37]
Chr8:8q24.21
uncertain significance
NR_003367.2(PVT1):n.971+7027A>G single nucleotide variant Lung cancer [RCV000107025] Chr8:127996318 [GRCh38]
Chr8:129008564 [GRCh37]
Chr8:8q24.21
uncertain significance
NR_003367.2(PVT1):n.972-36600G>T single nucleotide variant Lung cancer [RCV000107026] Chr8:128033560 [GRCh38]
Chr8:129045806 [GRCh37]
Chr8:8q24.21
uncertain significance
GRCh38/hg38 8q24.13-24.21(chr8:122454392-128513076)x3 copy number gain See cases [RCV000133620] Chr8:122454392..128513076 [GRCh38]
Chr8:123466631..129525322 [GRCh37]
Chr8:123535812..129594504 [NCBI36]
Chr8:8q24.13-24.21
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3 copy number gain See cases [RCV000134353] Chr8:94682154..145068656 [GRCh38]
Chr8:95694382..146294042 [GRCh37]
Chr8:95763558..146264846 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q21.3-24.23(chr8:86300584-137022587)x3 copy number gain See cases [RCV000135621] Chr8:86300584..137022587 [GRCh38]
Chr8:87312813..138034830 [GRCh37]
Chr8:87381929..138104012 [NCBI36]
Chr8:8q21.3-24.23
pathogenic|likely pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124498498-145068712)x3 copy number gain See cases [RCV000137346] Chr8:124498498..145068712 [GRCh38]
Chr8:125510739..146294098 [GRCh37]
Chr8:125579920..146264902 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8q21.3-24.3(chr8:87931152-145068712)x3 copy number gain See cases [RCV000138551] Chr8:87931152..145068712 [GRCh38]
Chr8:88943380..146294098 [GRCh37]
Chr8:89012496..146264902 [NCBI36]
Chr8:8q21.3-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:97382873-145070385)x3 copy number gain See cases [RCV000140447] Chr8:97382873..145070385 [GRCh38]
Chr8:98395101..146295771 [GRCh37]
Chr8:98464277..146266575 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3 copy number gain See cases [RCV000139539] Chr8:46031340..139285494 [GRCh38]
Chr8:46942962..140297737 [GRCh37]
Chr8:47062127..140366919 [NCBI36]
Chr8:8q11.1-24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:100867343-145070385)x3 copy number gain See cases [RCV000141694] Chr8:100867343..145070385 [GRCh38]
Chr8:101879571..146295771 [GRCh37]
Chr8:101948747..146266575 [NCBI36]
Chr8:8q22.3-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:103306336-145068712)x3 copy number gain See cases [RCV000142810] Chr8:103306336..145068712 [GRCh38]
Chr8:104318564..146294098 [GRCh37]
Chr8:104387740..146264902 [NCBI36]
Chr8:8q22.3-24.3
pathogenic|likely pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.2-24.3(chr8:85765999-145070385)x3 copy number gain See cases [RCV000143659] Chr8:85765999..145070385 [GRCh38]
Chr8:86778228..146295771 [GRCh37]
Chr8:86863079..146266575 [NCBI36]
Chr8:8q21.2-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000148117] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8q24.21(chr8:127118340-127858575)x3 copy number gain See cases [RCV000050763] Chr8:127118340..127858575 [GRCh38]
Chr8:128130585..128870821 [GRCh37]
Chr8:128199767..128940003 [NCBI36]
Chr8:8q24.21
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q22.1-24.3(chr8:98432250-146222672)x4 copy number gain See cases [RCV000448954] Chr8:98432250..146222672 [GRCh37]
Chr8:8q22.1-24.3
pathogenic
GRCh37/hg19 8q24.21-24.22(chr8:128295596-133200773)x1 copy number loss See cases [RCV000448960] Chr8:128295596..133200773 [GRCh37]
Chr8:8q24.21-24.22
likely pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q21.3-24.3(chr8:93047482-141355635)x3 copy number gain See cases [RCV000511761] Chr8:93047482..141355635 [GRCh37]
Chr8:8q21.3-24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841154-146295771)x3 copy number gain See cases [RCV000511002] Chr8:86841154..146295771 [GRCh37]
Chr8:8q21.2-24.3
pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841228-142689874)x3 copy number gain See cases [RCV000510854] Chr8:86841228..142689874 [GRCh37]
Chr8:8q21.2-24.3
pathogenic
GRCh37/hg19 8q23.3-24.3(chr8:114853126-146295771)x3 copy number gain See cases [RCV000512401] Chr8:114853126..146295771 [GRCh37]
Chr8:8q23.3-24.3
pathogenic
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3 copy number gain See cases [RCV000512169] Chr8:12490999..146295771 [GRCh37]
Chr8:8p23.1-q24.3
pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:121694649-146295771)x3 copy number gain not provided [RCV000683044] Chr8:121694649..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic
Single allele deletion Trichorhinophalangeal dysplasia type I [RCV000735900] Chr8:114508086..129040004 [GRCh37]
Chr8:8q23.3-24.21
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q24.13-24.3(chr8:126892814-143750028)x1 copy number loss not provided [RCV001006144] Chr8:126892814..143750028 [GRCh37]
Chr8:8q24.13-24.3
pathogenic
GRCh37/hg19 8q24.13-24.3(chr8:125496223-146295771)x3 copy number gain not provided [RCV000845705] Chr8:125496223..146295771 [GRCh37]
Chr8:8q24.13-24.3
pathogenic
GRCh37/hg19 8q24.13-24.22(chr8:124120772-135265846)x1 copy number loss not provided [RCV000848438] Chr8:124120772..135265846 [GRCh37]
Chr8:8q24.13-24.22
pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:122193546-146295771)x3 copy number gain not provided [RCV000849762] Chr8:122193546..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic
GRCh37/hg19 8q24.13-24.21(chr8:123074293-131113892)x1 copy number loss not provided [RCV000848164] Chr8:123074293..131113892 [GRCh37]
Chr8:8q24.13-24.21
pathogenic
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3 copy number gain not provided [RCV000848192] Chr8:31936551..146295771 [GRCh37]
Chr8:8p12-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q24.21-24.3(chr8:128877995-146295771)x3 copy number gain not provided [RCV001006146] Chr8:128877995..146295771 [GRCh37]
Chr8:8q24.21-24.3
pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:121042467-146295771)x3 copy number gain not provided [RCV001006140] Chr8:121042467..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:9709 AgrOrtholog
COSMIC PVT1 COSMIC
Ensembl Genes ENSG00000249859 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000513868 ENTREZGENE
GTEx ENSG00000249859 GTEx
HGNC ID HGNC:9709 ENTREZGENE
Human Proteome Map PVT1 Human Proteome Map
NCBI Gene 5820 ENTREZGENE
OMIM 165140 OMIM
PharmGKB PA34053 PharmGKB
RNAcentral URS00008E3A67 RNACentral


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-05-22 PVT1  Pvt1 oncogene    Pvt1 oncogene (non-protein coding)  Symbol and/or name change 5135510 APPROVED