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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:HEATR1-MKNK2 (FusionGDB2 ID:35945)

Fusion Gene Summary for HEATR1-MKNK2

check button Fusion gene summary
Fusion gene informationFusion gene name: HEATR1-MKNK2
Fusion gene ID: 35945
HgeneTgene
Gene symbol

HEATR1

MKNK2

Gene ID

55127

2872

Gene nameHEAT repeat containing 1MAPK interacting serine/threonine kinase 2
SynonymsBAP28|UTP10GPRK7|MNK2
Cytomap

1q43

19p13.3

Type of geneprotein-codingprotein-coding
DescriptionHEAT repeat-containing protein 1U3 small nucleolar RNA-associated protein 10 homologUTP10, small subunit (SSU) processome component, homologprotein BAP28MAP kinase-interacting serine/threonine-protein kinase 2G protein-coupled receptor kinase 7MAP kinase interacting serine/threonine kinase 2MAP kinase signal-integrating kinase 2MAPK signal-integrating kinase 2
Modification date2020031320200313
UniProtAcc

Q9H583

Q9HBH9

Ensembl transtripts involved in fusion geneENST00000366579, ENST00000366581, 
ENST00000366582, ENST00000483073, 
ENST00000591142, ENST00000250896, 
ENST00000309340, ENST00000591601, 
ENST00000541165, ENST00000588014, 
ENST00000591588, 
Fusion gene scores* DoF score6 X 7 X 5=2108 X 7 X 3=168
# samples 78
** MAII scorelog2(7/210*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/168*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HEATR1 [Title/Abstract] AND MKNK2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHEATR1(236713872)-MKNK2(2037806), # 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
TgeneMKNK2

GO:0006468

protein phosphorylation

11463832

TgeneMKNK2

GO:0030097

hemopoiesis

21149447

TgeneMKNK2

GO:0035556

intracellular signal transduction

11463832

TgeneMKNK2

GO:0071243

cellular response to arsenic-containing substance

18299328


check buttonFusion gene breakpoints across HEATR1 (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 MKNK2 (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
ChimerDB4Non-CancerERR315460HEATR1chr1

236713872

-MKNK2chr19

2037806

-


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Fusion Gene ORF analysis for HEATR1-MKNK2

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-3CDSENST00000366579ENST00000591142HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3CDSENST00000366581ENST00000591142HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3CDSENST00000366582ENST00000591142HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3CDSENST00000483073ENST00000591142HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000366579ENST00000250896HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000366579ENST00000309340HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000366579ENST00000591601HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000366581ENST00000250896HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000366581ENST00000309340HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000366581ENST00000591601HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000366582ENST00000250896HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000366582ENST00000309340HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000366582ENST00000591601HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000483073ENST00000250896HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000483073ENST00000309340HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-3UTRENST00000483073ENST00000591601HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000366579ENST00000541165HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000366579ENST00000588014HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000366579ENST00000591588HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000366581ENST00000541165HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000366581ENST00000588014HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000366581ENST00000591588HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000366582ENST00000541165HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000366582ENST00000588014HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000366582ENST00000591588HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000483073ENST00000541165HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000483073ENST00000588014HEATR1chr1

236713872

-MKNK2chr19

2037806

-
intron-intronENST00000483073ENST00000591588HEATR1chr1

236713872

-MKNK2chr19

2037806

-

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 HEATR1-MKNK2


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 HEATR1-MKNK2


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:236713872/:2037806)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
HEATR1

Q9H583

MKNK2

Q9HBH9

FUNCTION: Ribosome biogenesis factor. Involved in nucleolar processing of pre-18S ribosomal RNA. Required for optimal pre-ribosomal RNA transcription by RNA polymerase I. {ECO:0000269|PubMed:17699751}.FUNCTION: Serine/threonine-protein kinase that phosphorylates SFPQ/PSF, HNRNPA1 and EIF4E. May play a role in the response to environmental stress and cytokines. Appears to regulate translation by phosphorylating EIF4E, thus increasing the affinity of this protein for the 7-methylguanosine-containing mRNA cap. Required for mediating PP2A-inhibition-induced EIF4E phosphorylation. Triggers EIF4E shuttling from cytoplasm to nucleus. Isoform 1 displays a high basal kinase activity, but isoform 2 exhibits a very low kinase activity. Acts as a mediator of the suppressive effects of IFNgamma on hematopoiesis. Negative regulator for signals that control generation of arsenic trioxide As(2)O(3)-dependent apoptosis and anti-leukemic responses. Involved in anti-apoptotic signaling in response to serum withdrawal. {ECO:0000269|PubMed:11154262, ECO:0000269|PubMed:11463832, ECO:0000269|PubMed:12897141, ECO:0000269|PubMed:16111636, ECO:0000269|PubMed:17965020, ECO:0000269|PubMed:18299328, ECO:0000269|PubMed:20823271, ECO:0000269|PubMed:20927323, ECO:0000269|PubMed:21149447}.

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 HEATR1-MKNK2


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 HEATR1-MKNK2


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 HEATR1-MKNK2


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 HEATR1-MKNK2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource