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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:SLX4IP-CEP89 (FusionGDB2 ID:83747)

Fusion Gene Summary for SLX4IP-CEP89

check button Fusion gene summary
Fusion gene informationFusion gene name: SLX4IP-CEP89
Fusion gene ID: 83747
HgeneTgene
Gene symbol

SLX4IP

CEP89

Gene ID

128710

84902

Gene nameSLX4 interacting proteincentrosomal protein 89
SynonymsC20orf94|bA204H22.1|bA254M13.1|dJ1099D15.3CCDC123|CEP123
Cytomap

20p12.2

19q13.11

Type of geneprotein-codingprotein-coding
Descriptionprotein SLX4IPcentrosomal protein of 89 kDacentrosomal protein 123centrosomal protein 89kDacoiled-coil domain containing 123coiled-coil domain-containing protein 123, mitochondrial
Modification date2020031320200313
UniProtAcc

Q5VYV7

Q96ST8

Ensembl transtripts involved in fusion geneENST00000334534, ENST00000590597, 
ENST00000591863, ENST00000305768, 
Fusion gene scores* DoF score13 X 9 X 5=58511 X 11 X 7=847
# samples 1315
** MAII scorelog2(13/585*10)=-2.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/847*10)=-2.49739946883632
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SLX4IP [Title/Abstract] AND CEP89 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSLX4IP(10438879)-CEP89(33378747), # samples:2
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 SLX4IP (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across CEP89 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4OVTCGA-20-1683-01ASLX4IPchr20

10438879

+CEP89chr19

33378747

-


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Fusion Gene ORF analysis for SLX4IP-CEP89

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-intronENST00000334534ENST00000590597SLX4IPchr20

10438879

+CEP89chr19

33378747

-
5CDS-intronENST00000334534ENST00000591863SLX4IPchr20

10438879

+CEP89chr19

33378747

-
In-frameENST00000334534ENST00000305768SLX4IPchr20

10438879

+CEP89chr19

33378747

-

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)
ENST00000334534SLX4IPchr2010438879+ENST00000305768CEP89chr1933378747-850207803279174

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
ENST00000334534ENST00000305768SLX4IPchr2010438879+CEP89chr1933378747-0.0052690980.99473083

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Fusion Genomic Features for SLX4IP-CEP89


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.
genomic feature

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 SLX4IP-CEP89


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/chr20:10438879/chr19:33378747)
- 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
SLX4IP

Q5VYV7

CEP89

Q96ST8

FUNCTION: Required for ciliogenesis. Also plays a role in mitochondrial metabolism where it may modulate complex IV activity. {ECO:0000269|PubMed:23348840, ECO:0000269|PubMed:23575228}.

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
TgeneCEP89chr20:10438879chr19:33378747ENST0000059059709234_3330357.0Coiled coilOntology_term=ECO:0000255
TgeneCEP89chr20:10438879chr19:33378747ENST0000059059709369_7190357.0Coiled coilOntology_term=ECO:0000255

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneCEP89chr20:10438879chr19:33378747ENST000003057681519234_333625784.0Coiled coilOntology_term=ECO:0000255
TgeneCEP89chr20:10438879chr19:33378747ENST000003057681519369_719625784.0Coiled coilOntology_term=ECO:0000255


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Fusion Gene Sequence for SLX4IP-CEP89


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.
>83747_83747_1_SLX4IP-CEP89_SLX4IP_chr20_10438879_ENST00000334534_CEP89_chr19_33378747_ENST00000305768_length(transcript)=850nt_BP=207nt
GCGAAAGTGCTTCCCTTAAGCTTCTGAAGGTTGGCTGCAGTTCCGGCTACCTGTGTAGTCCGAGTTTCCACAGCCAGGTACTACTCCGCC
AGTGACCCTGGACAGTAACAAAACATATAAAGCCCGAGCCCAAACCCCGCCACCATCATAGGTCTGTAGTTACTGTGGAATCAATAAGCC
ATGGCATCTAAGAAATTTGCTGTTAAAGCAAAATGTTTAGAAAGTGAGAAGGATGGAGTGCTTAATAAAGTCATAAAAAGCAACATTCGC
CTGGGAAAGTTAGAGGAAAAAGTCAAGGGCTACAAGAAGCAGGCAGCACTGAAGCTGGGGGACATCAGTCACCGTCTGCTGGAGCAGCAG
GAGGACTTCGCCGGCAAGACAGCCCAGTACCGGCAGGAGATGCGGCACCTGCACCAGGTGCTGAAGGACAAGCAGGAGGTGCTGGACCAG
GCGCTGCAGCAGAACAGAGAAATGGAAGGTGAACTTGAAGTTATTTGGGAATCTACCTTCAGGGAAAACCGAAGAATCCGAGAACTTCTC
CAGGACACACTCACGAGGACAGGCGTGCAGGACAACCCCAGAGCTCTGGTTGCCCCCAGCCTCAATGGCGTCTCTCAGGCAGACCTGCTG
GACGGCTGCGATGTCTGCTCCTATGACCTGAAGTCTCATGCCCCCACCTGCTAGAATCTGCGGGAGCCCGTGGTGTAGCCTCCTCTGGCC
TGAAAGGTCTGCCTCACACAGGCCTTCCCTGCAGGGCAGCCCATGGTGGCAGCCGGAGGTGCGTAAGCCCACTGAACGCTGCAGGGCAGG

>83747_83747_1_SLX4IP-CEP89_SLX4IP_chr20_10438879_ENST00000334534_CEP89_chr19_33378747_ENST00000305768_length(amino acids)=174AA_BP=
MQRSVGLRTSGCHHGLPCREGLCEADLSGQRRLHHGLPQILAGGGMRLQVIGADIAAVQQVCLRDAIEAGGNQSSGVVLHACPRECVLEK

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Fusion Gene PPI Analysis for SLX4IP-CEP89


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 SLX4IP-CEP89


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 SLX4IP-CEP89


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