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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:MKLN1-HNRNPD (FusionGDB2 ID:54084)

Fusion Gene Summary for MKLN1-HNRNPD

check button Fusion gene summary
Fusion gene informationFusion gene name: MKLN1-HNRNPD
Fusion gene ID: 54084
HgeneTgene
Gene symbol

MKLN1

HNRNPD

Gene ID

4289

3184

Gene namemuskelin 1heterogeneous nuclear ribonucleoprotein D
SynonymsTWA2AUF1|AUF1A|HNRPD|P37|hnRNPD0
Cytomap

7q32.3

4q21.22

Type of geneprotein-codingprotein-coding
Descriptionmuskelinmuskelin 1, intracellular mediator containing kelch motifsheterogeneous nuclear ribonucleoprotein D0ARE-binding protein AUFI, type AAU-rich element RNA binding protein 1, 37kDahnRNP D0
Modification date2020031320200329
UniProtAcc.

O14979

Ensembl transtripts involved in fusion geneENST00000421797, ENST00000352689, 
ENST00000429546, ENST00000498778, 
ENST00000313899, ENST00000352301, 
ENST00000353341, ENST00000543098, 
ENST00000508119, ENST00000541060, 
Fusion gene scores* DoF score15 X 15 X 7=157519 X 13 X 8=1976
# samples 1619
** MAII scorelog2(16/1575*10)=-3.29920801838728
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(19/1976*10)=-3.37851162325373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MKLN1 [Title/Abstract] AND HNRNPD [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMKLN1(130827700)-HNRNPD(83280792), # 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

check buttonFusion gene breakpoints across MKLN1 (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 HNRNPD (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
ChimerDB4GBMTCGA-27-2526-01AMKLN1chr7

130827700

+HNRNPDchr4

83280792

-


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Fusion Gene ORF analysis for MKLN1-HNRNPD

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
5UTR-3CDSENST00000421797ENST00000313899MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
5UTR-3CDSENST00000421797ENST00000352301MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
5UTR-3CDSENST00000421797ENST00000353341MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
5UTR-3CDSENST00000421797ENST00000543098MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
5UTR-intronENST00000421797ENST00000508119MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
5UTR-intronENST00000421797ENST00000541060MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000352689ENST00000313899MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000352689ENST00000352301MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000352689ENST00000353341MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000352689ENST00000543098MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000429546ENST00000313899MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000429546ENST00000352301MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000429546ENST00000353341MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000429546ENST00000543098MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000498778ENST00000313899MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000498778ENST00000352301MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000498778ENST00000353341MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-3CDSENST00000498778ENST00000543098MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-intronENST00000352689ENST00000508119MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-intronENST00000352689ENST00000541060MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-intronENST00000429546ENST00000508119MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-intronENST00000429546ENST00000541060MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-intronENST00000498778ENST00000508119MKLN1chr7

130827700

+HNRNPDchr4

83280792

-
intron-intronENST00000498778ENST00000541060MKLN1chr7

130827700

+HNRNPDchr4

83280792

-

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 MKLN1-HNRNPD


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 MKLN1-HNRNPD


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/:130827700/:83280792)
- 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
.HNRNPD

O14979

FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Acts as a transcriptional regulator. Promotes transcription repression. Promotes transcription activation in differentiated myotubes (By similarity). Binds to double- and single-stranded DNA sequences. Binds to the transcription suppressor CATR sequence of the COX5B promoter (By similarity). Binds with high affinity to RNA molecules that contain AU-rich elements (AREs) found within the 3'-UTR of many proto-oncogenes and cytokine mRNAs. Binds both to nuclear and cytoplasmic poly(A) mRNAs. Binds to poly(G) and poly(A), but not to poly(U) or poly(C) RNA homopolymers. Binds to the 5'-ACUAGC-3' RNA consensus sequence. {ECO:0000250, ECO:0000269|PubMed:9538234}.

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 MKLN1-HNRNPD


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 MKLN1-HNRNPD


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 MKLN1-HNRNPD


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 MKLN1-HNRNPD


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