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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:CDH17-ESRP1 (FusionGDB2 ID:15076)

Fusion Gene Summary for CDH17-ESRP1

check button Fusion gene summary
Fusion gene informationFusion gene name: CDH17-ESRP1
Fusion gene ID: 15076
HgeneTgene
Gene symbol

CDH17

ESRP1

Gene ID

1015

54845

Gene namecadherin 17epithelial splicing regulatory protein 1
SynonymsCDH16|HPT-1|HPT1DFNB109|RBM35A|RMB35A
Cytomap

8q22.1

8q22.1

Type of geneprotein-codingprotein-coding
Descriptioncadherin-17HPT-1 cadherinLI cadherincadherin 17, LI cadherin (liver-intestine)cadherin-16human intestinal peptide-associated transporter HPT-1human peptide transporter 1intestinal peptide-associated transporter HPT-1liver-intestine cadherinepithelial splicing regulatory protein 1RNA-binding motif protein 35ARNA-binding protein 35A
Modification date2020031320200313
UniProtAcc.

Q6NXG1

Ensembl transtripts involved in fusion geneENST00000027335, ENST00000441892, 
ENST00000450165, 
ENST00000423620, 
ENST00000433389, ENST00000358397, 
ENST00000454170, ENST00000523347, 
Fusion gene scores* DoF score6 X 6 X 4=14414 X 16 X 7=1568
# samples 715
** MAII scorelog2(7/144*10)=-1.04064198449735
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/1568*10)=-3.38589115361933
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CDH17 [Title/Abstract] AND ESRP1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCDH17(95220711)-ESRP1(95718153), # 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
TgeneESRP1

GO:0043484

regulation of RNA splicing

19285943


check buttonFusion gene breakpoints across CDH17 (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 ESRP1 (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
ChimerDB4STADTCGA-BR-8077-01ACDH17chr8

95220711

-ESRP1chr8

95718153

+


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Fusion Gene ORF analysis for CDH17-ESRP1

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-3CDSENST00000027335ENST00000423620CDH17chr8

95220711

-ESRP1chr8

95718153

+
5UTR-3UTRENST00000027335ENST00000433389CDH17chr8

95220711

-ESRP1chr8

95718153

+
5UTR-3UTRENST00000027335ENST00000358397CDH17chr8

95220711

-ESRP1chr8

95718153

+
5UTR-3UTRENST00000027335ENST00000454170CDH17chr8

95220711

-ESRP1chr8

95718153

+
5UTR-3UTRENST00000027335ENST00000523347CDH17chr8

95220711

-ESRP1chr8

95718153

+
5UTR-3CDSENST00000441892ENST00000423620CDH17chr8

95220711

-ESRP1chr8

95718153

+
5UTR-3UTRENST00000441892ENST00000433389CDH17chr8

95220711

-ESRP1chr8

95718153

+
5UTR-3UTRENST00000441892ENST00000358397CDH17chr8

95220711

-ESRP1chr8

95718153

+
5UTR-3UTRENST00000441892ENST00000454170CDH17chr8

95220711

-ESRP1chr8

95718153

+
5UTR-3UTRENST00000441892ENST00000523347CDH17chr8

95220711

-ESRP1chr8

95718153

+
intron-3CDSENST00000450165ENST00000423620CDH17chr8

95220711

-ESRP1chr8

95718153

+
intron-3UTRENST00000450165ENST00000433389CDH17chr8

95220711

-ESRP1chr8

95718153

+
intron-3UTRENST00000450165ENST00000358397CDH17chr8

95220711

-ESRP1chr8

95718153

+
intron-3UTRENST00000450165ENST00000454170CDH17chr8

95220711

-ESRP1chr8

95718153

+
intron-3UTRENST00000450165ENST00000523347CDH17chr8

95220711

-ESRP1chr8

95718153

+

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 CDH17-ESRP1


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)
CDH17chr895220710-ESRP1chr895718152+0.0005389190.9994611
CDH17chr895220710-ESRP1chr895718152+0.0005389190.9994611

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 CDH17-ESRP1


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
.ESRP1

Q6NXG1

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: mRNA splicing factor that regulates the formation of epithelial cell-specific isoforms. Specifically regulates the expression of FGFR2-IIIb, an epithelial cell-specific isoform of FGFR2. Also regulates the splicing of CD44, CTNND1, ENAH, 3 transcripts that undergo changes in splicing during the epithelial-to-mesenchymal transition (EMT). Acts by directly binding specific sequences in mRNAs. Binds the GU-rich sequence motifs in the ISE/ISS-3, a cis-element regulatory region present in the mRNA of FGFR2 (PubMed:19285943). Regulates splicing and expression of genes involved in inner ear development, auditory hair cell differentiation, and cell fate specification in the cochlear epithelium (By similarity). {ECO:0000250|UniProtKB:Q3US41, ECO:0000269|PubMed:19285943}.

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 CDH17-ESRP1


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 CDH17-ESRP1


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 CDH17-ESRP1


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 CDH17-ESRP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCDH17C0005586Bipolar Disorder2PSYGENET
HgeneCDH17C0033975Psychotic Disorders1PSYGENET
HgeneCDH17C0264423Asthma, Occupational1CTD_human
HgeneCDH17C0349204Nonorganic psychosis1PSYGENET
HgeneCDH17C1839839MAJOR AFFECTIVE DISORDER 21PSYGENET
TgeneESRP1C4693935DEAFNESS, AUTOSOMAL RECESSIVE 1091GENOMICS_ENGLAND;UNIPROT