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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:PKM-VCAM1 (FusionGDB2 ID:65344)

Fusion Gene Summary for PKM-VCAM1

check button Fusion gene summary
Fusion gene informationFusion gene name: PKM-VCAM1
Fusion gene ID: 65344
HgeneTgene
Gene symbol

PKM

VCAM1

Gene ID

5315

7412

Gene namepyruvate kinase M1/2vascular cell adhesion molecule 1
SynonymsCTHBP|HEL-S-30|OIP3|PK3|PKM2|TCB|THBP1|p58CD106|INCAM-100
Cytomap

15q23

1p21.2

Type of geneprotein-codingprotein-coding
Descriptionpyruvate kinase PKMOPA-interacting protein 3PK, muscle typecytosolic thyroid hormone-binding proteinepididymis secretory protein Li 30pyruvate kinase 2/3pyruvate kinase isozymes M1/M2pyruvate kinase muscle isozymepyruvate kinase, musclethyroid hovascular cell adhesion protein 1CD106 antigen
Modification date2020032920200322
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000319622, ENST00000565184, 
ENST00000389093, ENST00000335181, 
ENST00000568883, ENST00000449901, 
ENST00000565154, ENST00000568459, 
ENST00000370119, ENST00000347652, 
ENST00000294728, ENST00000370115, 
Fusion gene scores* DoF score35 X 35 X 7=85754 X 4 X 1=16
# samples 414
** MAII scorelog2(41/8575*10)=-4.38644085644209
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/16*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: PKM [Title/Abstract] AND VCAM1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPKM(72499482)-VCAM1(101188620), # samples:1
Anticipated loss of major functional domain due to fusion event.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgenePKM

GO:0012501

programmed cell death

17308100

TgeneVCAM1

GO:0007155

cell adhesion

16809613

TgeneVCAM1

GO:0007157

heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules

1715889

TgeneVCAM1

GO:0007159

leukocyte cell-cell adhesion

1381355|1715889|2688898

TgeneVCAM1

GO:0007160

cell-matrix adhesion

18308860

TgeneVCAM1

GO:0009308

amine metabolic process

23474851

TgeneVCAM1

GO:0042102

positive regulation of T cell proliferation

1381355

TgeneVCAM1

GO:0050901

leukocyte tethering or rolling

18308860


check buttonFusion gene breakpoints across PKM (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across VCAM1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ABQ328230PKMchr15

72499482

-VCAM1chr1

101188620

+


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Fusion Gene ORF analysis for PKM-VCAM1

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
intron-3CDSENST00000319622ENST00000370119PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000319622ENST00000347652PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000319622ENST00000294728PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000319622ENST00000370115PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000565184ENST00000370119PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000565184ENST00000347652PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000565184ENST00000294728PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000565184ENST00000370115PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000389093ENST00000370119PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000389093ENST00000347652PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000389093ENST00000294728PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000389093ENST00000370115PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000335181ENST00000370119PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000335181ENST00000347652PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000335181ENST00000294728PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000335181ENST00000370115PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000568883ENST00000370119PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000568883ENST00000347652PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000568883ENST00000294728PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000568883ENST00000370115PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000449901ENST00000370119PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000449901ENST00000347652PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000449901ENST00000294728PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000449901ENST00000370115PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000565154ENST00000370119PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000565154ENST00000347652PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000565154ENST00000294728PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000565154ENST00000370115PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000568459ENST00000370119PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000568459ENST00000347652PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000568459ENST00000294728PKMchr15

72499482

-VCAM1chr1

101188620

+
intron-3CDSENST00000568459ENST00000370115PKMchr15

72499482

-VCAM1chr1

101188620

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for PKM-VCAM1


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for PKM-VCAM1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for PKM-VCAM1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for PKM-VCAM1


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for PKM-VCAM1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for PKM-VCAM1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePKMC0027626Neoplasm Invasiveness2CTD_human
HgenePKMC0001787Osteoporosis, Age-Related1CTD_human
HgenePKMC0007097Carcinoma1CTD_human
HgenePKMC0024667Animal Mammary Neoplasms1CTD_human
HgenePKMC0024668Mammary Neoplasms, Experimental1CTD_human
HgenePKMC0029456Osteoporosis1CTD_human
HgenePKMC0029459Osteoporosis, Senile1CTD_human
HgenePKMC0205696Anaplastic carcinoma1CTD_human
HgenePKMC0205697Carcinoma, Spindle-Cell1CTD_human
HgenePKMC0205698Undifferentiated carcinoma1CTD_human
HgenePKMC0205699Carcinomatosis1CTD_human
HgenePKMC0751406Post-Traumatic Osteoporosis1CTD_human
HgenePKMC1257925Mammary Carcinoma, Animal1CTD_human
HgenePKMC2239176Liver carcinoma1CTD_human
TgeneVCAM1C0007222Cardiovascular Diseases2CTD_human
TgeneVCAM1C0020538Hypertensive disease2CTD_human
TgeneVCAM1C0002895Anemia, Sickle Cell1CTD_human
TgeneVCAM1C0004153Atherosclerosis1CTD_human
TgeneVCAM1C0008370Cholestasis1CTD_human
TgeneVCAM1C0009324Ulcerative Colitis1CTD_human
TgeneVCAM1C0011603Dermatitis1CTD_human
TgeneVCAM1C0019284Diaphragmatic Hernia1CTD_human
TgeneVCAM1C0020443Hypercholesterolemia1CTD_human
TgeneVCAM1C0026769Multiple Sclerosis1CTD_human
TgeneVCAM1C0041948Uremia1CTD_human
TgeneVCAM1C0042109Urticaria1CTD_human
TgeneVCAM1C0151744Myocardial Ischemia1CTD_human
TgeneVCAM1C0268318Cholestasis of pregnancy1CTD_human
TgeneVCAM1C0751324Multiple Sclerosis, Acute Fulminating1CTD_human
TgeneVCAM1C1563937Atherogenesis1CTD_human
TgeneVCAM1C2239176Liver carcinoma1CTD_human
TgeneVCAM1C3489728Familial intrahepatic cholestasis of pregnancy1CTD_human