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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:KIAA1033-PCDH9

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: KIAA1033-PCDH9
FusionPDB ID: 42217
FusionGDB2.0 ID: 42217
HgeneTgene
Gene symbol

KIAA1033

PCDH9

Gene ID

23325

5101

Gene nameWASH complex subunit 4protocadherin 9
SynonymsKIAA1033|MRT43|SWIP-
Cytomap

12q23.3

13q21.32

Type of geneprotein-codingprotein-coding
DescriptionWASH complex subunit 4WASH complex subunit 7WASH complex subunit SWIPstrumpellin and WASH-interacting proteinprotocadherin-9cadherin superfamily protein VR4-11
Modification date2020032020200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000332180, ENST00000547171, 
ENST00000328454, ENST00000377861, 
ENST00000456367, ENST00000377865, 
ENST00000544246, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 5=18013 X 11 X 4=572
# samples 713
** MAII scorelog2(7/180*10)=-1.36257007938471
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/572*10)=-2.13750352374993
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: KIAA1033 [Title/Abstract] AND PCDH9 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)KIAA1033(105534179)-PCDH9(67477737), # samples:1
Anticipated loss of major functional domain due to fusion event.KIAA1033-PCDH9 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
KIAA1033-PCDH9 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
KIAA1033-PCDH9 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
KIAA1033-PCDH9 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
* 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 KIAA1033 (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 PCDH9 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4LUSCTCGA-46-6025-01AKIAA1033chr12

105534179

-PCDH9chr13

67477737

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000332180KIAA1033chr12105534179-ENST00000544246PCDH9chr1367477737-41451647512324757
ENST00000332180KIAA1033chr12105534179-ENST00000377865PCDH9chr1367477737-41431647512324757

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
ENST00000332180ENST00000544246KIAA1033chr12105534179-PCDH9chr1367477737-0.0002938680.9997061
ENST00000332180ENST00000377865KIAA1033chr12105534179-PCDH9chr1367477737-0.0002930780.9997069

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>42217_42217_1_KIAA1033-PCDH9_KIAA1033_chr12_105534179_ENST00000332180_PCDH9_chr13_67477737_ENST00000377865_length(amino acids)=757AA_BP=532
MVGAVSVGGAGVMAVETLSPDWEFDRVDDGSQKIHAEVQLKNYGKFLEEYTSQLRRIEDALDDSIGDVWDFNLDPIALKLLPYEQSSLLE
LIKTENKVLNKVITVYAALCCEIKKLKYEAETKFYNGLLFYGEGATDASMVEGDCQIQMGRFISFLQELSCFVTRCYEVVMNVVHQLAAL
YISNKIAPKIIETTGVHFQTMYEHLGELLTVLLTLDEIIDNHITLKDHWTMYKRLLKSVHHNPSKFGIQEEKLKPFEKFLLKLEGQLLDG
MIFQACIEQQFDSLNGGVSVSKNSTFAEEFAHSIRSIFANVEAKLGEPSEIDQRDKYVGICGLFVLHFQIFRTIDKKFYKSLLDICKKVP
AITLTANIIWFPDNFLIQKIPAAAKLLDRKSLQAIKIHRDTFLQQKAQSLTKDVQSYYVFVSSWMMKMESILSKEQRMDKFAEDLTNRCN
VFIQGFLYAYSISTIIKTTMNLYMSMQKPMTKTSVKALCRLVELLKAIEHMFYRRSMVVADSVSHITQHLQHQALHSISVAKCNSHSKSD
NIPVTPQKCPSSTGFHIQENEESHYESQRRVTFHLPDGSQESCSDSGLGDHEPVGSGTLISHPLPLVQPQDEFYDQASPDKRTEADGNSD
PNSDGPLGPRGLAEATEMCTQECLVLGHSDNCWMPPGLGPYQHPKSPLSTFAPQKEWVKKDKLVNGHTLTRAWKEDSNRNQFNDRKQYGS

--------------------------------------------------------------

>42217_42217_2_KIAA1033-PCDH9_KIAA1033_chr12_105534179_ENST00000332180_PCDH9_chr13_67477737_ENST00000544246_length(amino acids)=757AA_BP=532
MVGAVSVGGAGVMAVETLSPDWEFDRVDDGSQKIHAEVQLKNYGKFLEEYTSQLRRIEDALDDSIGDVWDFNLDPIALKLLPYEQSSLLE
LIKTENKVLNKVITVYAALCCEIKKLKYEAETKFYNGLLFYGEGATDASMVEGDCQIQMGRFISFLQELSCFVTRCYEVVMNVVHQLAAL
YISNKIAPKIIETTGVHFQTMYEHLGELLTVLLTLDEIIDNHITLKDHWTMYKRLLKSVHHNPSKFGIQEEKLKPFEKFLLKLEGQLLDG
MIFQACIEQQFDSLNGGVSVSKNSTFAEEFAHSIRSIFANVEAKLGEPSEIDQRDKYVGICGLFVLHFQIFRTIDKKFYKSLLDICKKVP
AITLTANIIWFPDNFLIQKIPAAAKLLDRKSLQAIKIHRDTFLQQKAQSLTKDVQSYYVFVSSWMMKMESILSKEQRMDKFAEDLTNRCN
VFIQGFLYAYSISTIIKTTMNLYMSMQKPMTKTSVKALCRLVELLKAIEHMFYRRSMVVADSVSHITQHLQHQALHSISVAKCNSHSKSD
NIPVTPQKCPSSTGFHIQENEESHYESQRRVTFHLPDGSQESCSDSGLGDHEPVGSGTLISHPLPLVQPQDEFYDQASPDKRTEADGNSD
PNSDGPLGPRGLAEATEMCTQECLVLGHSDNCWMPPGLGPYQHPKSPLSTFAPQKEWVKKDKLVNGHTLTRAWKEDSNRNQFNDRKQYGS

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Fusion Protein Functional Features


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/chr12:105534179/chr13:67477737)
- 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
..
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: 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.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgenePCDH9chr12:105534179chr13:67477737ENST0000032845403143_2520.01204.0DomainCadherin 2
TgenePCDH9chr12:105534179chr13:67477737ENST0000032845403253_3580.01204.0DomainCadherin 3
TgenePCDH9chr12:105534179chr13:67477737ENST000003284540326_1420.01204.0DomainCadherin 1
TgenePCDH9chr12:105534179chr13:67477737ENST0000032845403365_4690.01204.0DomainCadherin 4
TgenePCDH9chr12:105534179chr13:67477737ENST0000032845403470_5720.01204.0DomainCadherin 5
TgenePCDH9chr12:105534179chr13:67477737ENST0000032845403573_6750.01204.0DomainCadherin 6
TgenePCDH9chr12:105534179chr13:67477737ENST0000032845403679_7840.01204.0DomainCadherin 7
TgenePCDH9chr12:105534179chr13:67477737ENST0000045636704143_25201204.0DomainCadherin 2
TgenePCDH9chr12:105534179chr13:67477737ENST0000045636704253_35801204.0DomainCadherin 3
TgenePCDH9chr12:105534179chr13:67477737ENST000004563670426_14201204.0DomainCadherin 1
TgenePCDH9chr12:105534179chr13:67477737ENST0000045636704365_46901204.0DomainCadherin 4
TgenePCDH9chr12:105534179chr13:67477737ENST0000045636704470_57201204.0DomainCadherin 5
TgenePCDH9chr12:105534179chr13:67477737ENST0000045636704573_67501204.0DomainCadherin 6
TgenePCDH9chr12:105534179chr13:67477737ENST0000045636704679_78401204.0DomainCadherin 7
TgenePCDH9chr12:105534179chr13:67477737ENST000003284540324_8140.01204.0Topological domainExtracellular
TgenePCDH9chr12:105534179chr13:67477737ENST0000032845403836_12370.01204.0Topological domainCytoplasmic
TgenePCDH9chr12:105534179chr13:67477737ENST000004563670424_81401204.0Topological domainExtracellular
TgenePCDH9chr12:105534179chr13:67477737ENST0000045636704836_123701204.0Topological domainCytoplasmic
TgenePCDH9chr12:105534179chr13:67477737ENST0000032845403815_8350.01204.0TransmembraneHelical
TgenePCDH9chr12:105534179chr13:67477737ENST0000045636704815_83501204.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneKIAA1033chr12:105534179chr13:67477737ENST00000332180-16331135_1161520.01174.0Coiled coilOntology_term=ECO:0000255
TgenePCDH9chr12:105534179chr13:67477737ENST0000037786504143_2521012.01238.0DomainCadherin 2
TgenePCDH9chr12:105534179chr13:67477737ENST0000037786504253_3581012.01238.0DomainCadherin 3
TgenePCDH9chr12:105534179chr13:67477737ENST000003778650426_1421012.01238.0DomainCadherin 1
TgenePCDH9chr12:105534179chr13:67477737ENST0000037786504365_4691012.01238.0DomainCadherin 4
TgenePCDH9chr12:105534179chr13:67477737ENST0000037786504470_5721012.01238.0DomainCadherin 5
TgenePCDH9chr12:105534179chr13:67477737ENST0000037786504573_6751012.01238.0DomainCadherin 6
TgenePCDH9chr12:105534179chr13:67477737ENST0000037786504679_7841012.01238.0DomainCadherin 7
TgenePCDH9chr12:105534179chr13:67477737ENST0000054424615143_2521012.01238.0DomainCadherin 2
TgenePCDH9chr12:105534179chr13:67477737ENST0000054424615253_3581012.01238.0DomainCadherin 3
TgenePCDH9chr12:105534179chr13:67477737ENST000005442461526_1421012.01238.0DomainCadherin 1
TgenePCDH9chr12:105534179chr13:67477737ENST0000054424615365_4691012.01238.0DomainCadherin 4
TgenePCDH9chr12:105534179chr13:67477737ENST0000054424615470_5721012.01238.0DomainCadherin 5
TgenePCDH9chr12:105534179chr13:67477737ENST0000054424615573_6751012.01238.0DomainCadherin 6
TgenePCDH9chr12:105534179chr13:67477737ENST0000054424615679_7841012.01238.0DomainCadherin 7
TgenePCDH9chr12:105534179chr13:67477737ENST000003778650424_8141012.01238.0Topological domainExtracellular
TgenePCDH9chr12:105534179chr13:67477737ENST0000037786504836_12371012.01238.0Topological domainCytoplasmic
TgenePCDH9chr12:105534179chr13:67477737ENST000005442461524_8141012.01238.0Topological domainExtracellular
TgenePCDH9chr12:105534179chr13:67477737ENST0000054424615836_12371012.01238.0Topological domainCytoplasmic
TgenePCDH9chr12:105534179chr13:67477737ENST0000037786504815_8351012.01238.0TransmembraneHelical
TgenePCDH9chr12:105534179chr13:67477737ENST0000054424615815_8351012.01238.0TransmembraneHelical


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
KIAA1033
PCDH9


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to KIAA1033-PCDH9


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to KIAA1033-PCDH9


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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