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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:HNRNPM-CERS4 (FusionGDB2 ID:37270)

Fusion Gene Summary for HNRNPM-CERS4

check button Fusion gene summary
Fusion gene informationFusion gene name: HNRNPM-CERS4
Fusion gene ID: 37270
HgeneTgene
Gene symbol

HNRNPM

CERS4

Gene ID

4670

79603

Gene nameheterogeneous nuclear ribonucleoprotein Mceramide synthase 4
SynonymsCEAR|HNRNPM4|HNRPM|HNRPM4|HTGR1|NAGR1|hnRNP MLASS4|Trh1
Cytomap

19p13.2

19p13.2

Type of geneprotein-codingprotein-coding
Descriptionheterogeneous nuclear ribonucleoprotein MCEA receptorN-acetylglucosamine receptor 1heterogenous nuclear ribonucleoprotein M4hnRNA-binding protein M4ceramide synthase 4LAG1 homolog, ceramide synthase 4LAG1 longevity assurance homolog 4sphingosine N-acyltransferase CERS4
Modification date2020032220200320
UniProtAcc

P52272

Q9HA82

Ensembl transtripts involved in fusion geneENST00000325495, ENST00000348943, 
ENST00000602219, 		ENST00000251363, 
ENST00000559336, ENST00000559450, 
ENST00000558331, ENST00000595722, 
Fusion gene scores* DoF score16 X 12 X 10=192011 X 14 X 5=770
# samples 1915
** MAII scorelog2(19/1920*10)=-3.33703498727757
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(15/770*10)=-2.35989594508638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HNRNPM [Title/Abstract] AND CERS4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHNRNPM(8509995)-CERS4(8315960), # samples:3
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
TgeneCERS4

GO:0046513

ceramide biosynthetic process

17977534|29632068


check buttonFusion gene breakpoints across HNRNPM (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 CERS4 (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
ChimerDB4BRCATCGA-A8-A09Q-01AHNRNPMchr19

8509995

-CERS4chr19

8315960

+
ChimerDB4BRCATCGA-A8-A09Q-01AHNRNPMchr19

8509995

+CERS4chr19

8315960

+
ChimerDB4BRCATCGA-A8-A09QHNRNPMchr19

8509995

+CERS4chr19

8315959

+


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Fusion Gene ORF analysis for HNRNPM-CERS4

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
5CDS-5UTRENST00000325495ENST00000251363HNRNPMchr19

8509995

+CERS4chr19

8315960

+
5CDS-5UTRENST00000325495ENST00000251363HNRNPMchr19

8509995

+CERS4chr19

8315959

+
5CDS-5UTRENST00000325495ENST00000559336HNRNPMchr19

8509995

+CERS4chr19

8315960

+
5CDS-5UTRENST00000325495ENST00000559336HNRNPMchr19

8509995

+CERS4chr19

8315959

+
5CDS-5UTRENST00000325495ENST00000559450HNRNPMchr19

8509995

+CERS4chr19

8315960

+
5CDS-5UTRENST00000325495ENST00000559450HNRNPMchr19

8509995

+CERS4chr19

8315959

+
5CDS-5UTRENST00000348943ENST00000251363HNRNPMchr19

8509995

+CERS4chr19

8315960

+
5CDS-5UTRENST00000348943ENST00000251363HNRNPMchr19

8509995

+CERS4chr19

8315959

+
5CDS-5UTRENST00000348943ENST00000559336HNRNPMchr19

8509995

+CERS4chr19

8315960

+
5CDS-5UTRENST00000348943ENST00000559336HNRNPMchr19

8509995

+CERS4chr19

8315959

+
5CDS-5UTRENST00000348943ENST00000559450HNRNPMchr19

8509995

+CERS4chr19

8315960

+
5CDS-5UTRENST00000348943ENST00000559450HNRNPMchr19

8509995

+CERS4chr19

8315959

+
5CDS-intronENST00000325495ENST00000558331HNRNPMchr19

8509995

+CERS4chr19

8315960

+
5CDS-intronENST00000325495ENST00000558331HNRNPMchr19

8509995

+CERS4chr19

8315959

+
5CDS-intronENST00000325495ENST00000595722HNRNPMchr19

8509995

+CERS4chr19

8315960

+
5CDS-intronENST00000325495ENST00000595722HNRNPMchr19

8509995

+CERS4chr19

8315959

+
5CDS-intronENST00000348943ENST00000558331HNRNPMchr19

8509995

+CERS4chr19

8315960

+
5CDS-intronENST00000348943ENST00000558331HNRNPMchr19

8509995

+CERS4chr19

8315959

+
5CDS-intronENST00000348943ENST00000595722HNRNPMchr19

8509995

+CERS4chr19

8315960

+
5CDS-intronENST00000348943ENST00000595722HNRNPMchr19

8509995

+CERS4chr19

8315959

+
intron-5UTRENST00000602219ENST00000251363HNRNPMchr19

8509995

+CERS4chr19

8315960

+
intron-5UTRENST00000602219ENST00000251363HNRNPMchr19

8509995

+CERS4chr19

8315959

+
intron-5UTRENST00000602219ENST00000559336HNRNPMchr19

8509995

+CERS4chr19

8315960

+
intron-5UTRENST00000602219ENST00000559336HNRNPMchr19

8509995

+CERS4chr19

8315959

+
intron-5UTRENST00000602219ENST00000559450HNRNPMchr19

8509995

+CERS4chr19

8315960

+
intron-5UTRENST00000602219ENST00000559450HNRNPMchr19

8509995

+CERS4chr19

8315959

+
intron-intronENST00000602219ENST00000558331HNRNPMchr19

8509995

+CERS4chr19

8315960

+
intron-intronENST00000602219ENST00000558331HNRNPMchr19

8509995

+CERS4chr19

8315959

+
intron-intronENST00000602219ENST00000595722HNRNPMchr19

8509995

+CERS4chr19

8315960

+
intron-intronENST00000602219ENST00000595722HNRNPMchr19

8509995

+CERS4chr19

8315959

+

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 HNRNPM-CERS4


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)
HNRNPMchr198509995+CERS4chr198315959+6.19E-101
HNRNPMchr198509995+CERS4chr198315959+6.19E-101
HNRNPMchr198509995+CERS4chr198315959+6.19E-101
HNRNPMchr198509995+CERS4chr198315959+6.19E-101

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.
genomic feature of top 1%

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Fusion Protein Features for HNRNPM-CERS4


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/:8509995/:8315960)
- 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
HNRNPM

P52272

CERS4

Q9HA82

FUNCTION: Pre-mRNA binding protein in vivo, binds avidly to poly(G) and poly(U) RNA homopolymers in vitro. Involved in splicing. Acts as a receptor for carcinoembryonic antigen in Kupffer cells, may initiate a series of signaling events leading to tyrosine phosphorylation of proteins and induction of IL-1 alpha, IL-6, IL-10 and tumor necrosis factor alpha cytokines.FUNCTION: Ceramide synthase that catalyzes formation of ceramide from sphinganine and acyl-CoA substrates, with high selectivity toward long and very-long chains (C18:0-C22:0) as acyl donor. {ECO:0000269|PubMed:17977534, ECO:0000269|PubMed:23530041, ECO:0000269|PubMed:26887952, ECO:0000269|PubMed:29632068, ECO:0000269|PubMed:31916624}.

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 HNRNPM-CERS4


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 HNRNPM-CERS4


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 HNRNPM-CERS4


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 HNRNPM-CERS4


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