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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:SLC39A11-C17orf80 (FusionGDB2 ID:83132)

Fusion Gene Summary for SLC39A11-C17orf80

check button Fusion gene summary
Fusion gene informationFusion gene name: SLC39A11-C17orf80
Fusion gene ID: 83132
HgeneTgene
Gene symbol

SLC39A11

C17orf80

Gene ID

201266

55028

Gene namesolute carrier family 39 member 11chromosome 17 open reading frame 80
SynonymsC17orf26|ZIP-11|ZIP11HLC-8|MIG3|SPEP1
Cytomap

17q24.3-q25.1

17q25.1

Type of geneprotein-codingprotein-coding
Descriptionzinc transporter ZIP11Zrt- and Irt-like protein 11solute carrier family 39 (metal ion transporter), member 11uncharacterized protein C17orf80cell migration-inducing gene 3 proteinhuman lung cancer oncogene 8 proteinlung cancer-related protein 8sperm-expressed protein 1
Modification date2020031320200313
UniProtAcc.

Q9BSJ5

Ensembl transtripts involved in fusion geneENST00000255559, ENST00000542342, 
ENST00000579732, ENST00000579988, 
ENST00000255557, ENST00000268942, 
ENST00000359042, ENST00000426147, 
ENST00000535032, ENST00000577615, 
ENST00000582793, 
Fusion gene scores* DoF score28 X 24 X 11=73925 X 5 X 3=75
# samples 355
** MAII scorelog2(35/7392*10)=-4.40053792958373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SLC39A11 [Title/Abstract] AND C17orf80 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSLC39A11(71084796)-C17orf80(71231615), # 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 SLC39A11 (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 C17orf80 (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-AC-A5XU-01ASLC39A11chr17

71084796

-C17orf80chr17

71231615

+


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Fusion Gene ORF analysis for SLC39A11-C17orf80

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-5UTRENST00000255559ENST00000255557SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000255559ENST00000268942SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000255559ENST00000359042SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000255559ENST00000426147SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000255559ENST00000535032SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000255559ENST00000577615SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000542342ENST00000255557SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000542342ENST00000268942SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000542342ENST00000359042SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000542342ENST00000426147SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000542342ENST00000535032SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000542342ENST00000577615SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000579732ENST00000255557SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000579732ENST00000268942SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000579732ENST00000359042SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000579732ENST00000426147SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000579732ENST00000535032SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-5UTRENST00000579732ENST00000577615SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-intronENST00000255559ENST00000582793SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-intronENST00000542342ENST00000582793SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
5CDS-intronENST00000579732ENST00000582793SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
intron-5UTRENST00000579988ENST00000255557SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
intron-5UTRENST00000579988ENST00000268942SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
intron-5UTRENST00000579988ENST00000359042SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
intron-5UTRENST00000579988ENST00000426147SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
intron-5UTRENST00000579988ENST00000535032SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
intron-5UTRENST00000579988ENST00000577615SLC39A11chr17

71084796

-C17orf80chr17

71231615

+
intron-intronENST00000579988ENST00000582793SLC39A11chr17

71084796

-C17orf80chr17

71231615

+

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 SLC39A11-C17orf80


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)
SLC39A11chr1771084795-C17orf80chr1771231614+2.00E-060.999998
SLC39A11chr1771084795-C17orf80chr1771231614+2.00E-060.999998

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 SLC39A11-C17orf80


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/:71084796/:71231615)
- 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
.C17orf80

Q9BSJ5

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}.

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 SLC39A11-C17orf80


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 SLC39A11-C17orf80


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 SLC39A11-C17orf80


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 SLC39A11-C17orf80


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