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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:TEK-MAN1A1 (FusionGDB2 ID:89397)

Fusion Gene Summary for TEK-MAN1A1

check button Fusion gene summary
Fusion gene informationFusion gene name: TEK-MAN1A1
Fusion gene ID: 89397
HgeneTgene
Gene symbol

TEK

MAN1A1

Gene ID

7010

4121

Gene nameTEK receptor tyrosine kinasemannosidase alpha class 1A member 1
SynonymsCD202B|GLC3E|TIE-2|TIE2|VMCM|VMCM1HUMM3|HUMM9|MAN9
Cytomap

9p21.2

6q22.31

Type of geneprotein-codingprotein-coding
Descriptionangiopoietin-1 receptorTEK tyrosine kinase, endothelialendothelial tyrosine kinasetunica interna endothelial cell kinasetyrosine kinase with Ig and EGF homology domains-2tyrosine-protein kinase receptor TEKtyrosine-protein kinase receptor TIE-2mannosyl-oligosaccharide 1,2-alpha-mannosidase IAMan9-mannosidasealpha-1,2-mannosidase IAman(9)-alpha-mannosidaseprocessing alpha-1,2-mannosidase IA
Modification date2020032220200313
UniProtAcc.

P33908

Ensembl transtripts involved in fusion geneENST00000519097, ENST00000380036, 
ENST00000406359, 
ENST00000368468, 
ENST00000368466, 
Fusion gene scores* DoF score3 X 3 X 1=98 X 6 X 2=96
# samples 38
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(8/96*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TEK [Title/Abstract] AND MAN1A1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTEK(27160653)-MAN1A1(119670089), # 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
HgeneTEK

GO:0001934

positive regulation of protein phosphorylation

15284220

HgeneTEK

GO:0007169

transmembrane receptor protein tyrosine kinase signaling pathway

15284220

HgeneTEK

GO:0010595

positive regulation of endothelial cell migration

15284220

HgeneTEK

GO:0018108

peptidyl-tyrosine phosphorylation

11513602

HgeneTEK

GO:0045766

positive regulation of angiogenesis

15284220

HgeneTEK

GO:0046777

protein autophosphorylation

11513602

HgeneTEK

GO:0048014

Tie signaling pathway

15284220|19223473

HgeneTEK

GO:0051897

positive regulation of protein kinase B signaling

19615361

HgeneTEK

GO:0070374

positive regulation of ERK1 and ERK2 cascade

19615361


check buttonFusion gene breakpoints across TEK (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 MAN1A1 (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/AX74837TEKchr9

27160653

-MAN1A1chr6

119670089

-


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Fusion Gene ORF analysis for TEK-MAN1A1

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-3CDSENST00000519097ENST00000368468TEKchr9

27160653

-MAN1A1chr6

119670089

-
intron-3CDSENST00000519097ENST00000368466TEKchr9

27160653

-MAN1A1chr6

119670089

-
intron-3CDSENST00000380036ENST00000368468TEKchr9

27160653

-MAN1A1chr6

119670089

-
intron-3CDSENST00000380036ENST00000368466TEKchr9

27160653

-MAN1A1chr6

119670089

-
intron-3CDSENST00000406359ENST00000368468TEKchr9

27160653

-MAN1A1chr6

119670089

-
intron-3CDSENST00000406359ENST00000368466TEKchr9

27160653

-MAN1A1chr6

119670089

-

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 TEK-MAN1A1


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 TEK-MAN1A1


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
.MAN1A1

P33908

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: Involved in the maturation of Asn-linked oligosaccharides. Progressively trim alpha-1,2-linked mannose residues from Man(9)GlcNAc(2) to produce Man(5)GlcNAc(2).

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 TEK-MAN1A1


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 TEK-MAN1A1


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 TEK-MAN1A1


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 TEK-MAN1A1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTEKC1838437VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL5CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneTEKC0014556Epilepsy, Temporal Lobe1CTD_human
HgeneTEKC0014558Uncinate Epilepsy1CTD_human
HgeneTEKC0018923Hemangiosarcoma1CTD_human
HgeneTEKC0019207Hepatoma, Morris1CTD_human
HgeneTEKC0019208Hepatoma, Novikoff1CTD_human
HgeneTEKC0020302Hydrophthalmos1ORPHANET
HgeneTEKC0023904Liver Neoplasms, Experimental1CTD_human
HgeneTEKC0027686Pathologic Neovascularization1CTD_human
HgeneTEKC0086404Experimental Hepatoma1CTD_human
HgeneTEKC0346072Blue rubber bleb nevus syndrome1ORPHANET
HgeneTEKC0393672Epilepsy, Benign Psychomotor, Childhood1CTD_human
HgeneTEKC0393682Epilepsy, Lateral Temporal1CTD_human
HgeneTEKC4310639GLAUCOMA 3, PRIMARY CONGENITAL, E1CTD_human;UNIPROT