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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:APOH-C1S

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: APOH-C1S
FusionPDB ID: 5603
FusionGDB2.0 ID: 5603
HgeneTgene
Gene symbol

APOH

C1S

Gene ID

350

716

Gene nameapolipoprotein Hcomplement C1s
SynonymsB2G1|B2GP1|BGEDSPD2
Cytomap

17q24.2

12p13.31

Type of geneprotein-codingprotein-coding
Descriptionbeta-2-glycoprotein 1APC inhibitorB2GPIactivated protein C-binding proteinanticardiolipin cofactorapo-Hapolipoprotein H (beta-2-glycoprotein I)beta(2)GPIepididymis secretory sperm binding proteincomplement C1s subcomponentC1 esterasebasic proline-rich peptide IB-1complement component 1 subcomponent scomplement component 1, s subcomponent
Modification date2020031320200313
UniProtAcc

P02749

P09871

Ensembl transtripts involved in fusion geneENST idsENST00000205948, ENST00000402681, 
ENST00000495061, ENST00000328916, 
ENST00000360817, ENST00000406697, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score5 X 4 X 2=4010 X 11 X 3=330
# samples 510
** MAII scorelog2(5/40*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(10/330*10)=-1.72246602447109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: APOH [Title/Abstract] AND C1S [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)APOH(64216672)-C1S(7171571), # samples:1
Anticipated loss of major functional domain due to fusion event.APOH-C1S 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.
APOH-C1S 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.
APOH-C1S 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.
APOH-C1S 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
HgeneAPOH

GO:0001937

negative regulation of endothelial cell proliferation

17872974

HgeneAPOH

GO:0006641

triglyceride metabolic process

7417307

HgeneAPOH

GO:0007597

blood coagulation, intrinsic pathway

4052628

HgeneAPOH

GO:0010596

negative regulation of endothelial cell migration

17872974

HgeneAPOH

GO:0016525

negative regulation of angiogenesis

17872974

HgeneAPOH

GO:0030195

negative regulation of blood coagulation

4052628

HgeneAPOH

GO:0031639

plasminogen activation

16480936

HgeneAPOH

GO:0033033

negative regulation of myeloid cell apoptotic process

15534879

HgeneAPOH

GO:0034392

negative regulation of smooth muscle cell apoptotic process

15534879

HgeneAPOH

GO:0051006

positive regulation of lipoprotein lipase activity

7417307

HgeneAPOH

GO:0051917

regulation of fibrinolysis

16480936

HgeneAPOH

GO:0051918

negative regulation of fibrinolysis

14726399


check buttonFusion gene breakpoints across APOH (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 C1S (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
ChimerDB4LIHCTCGA-BC-A10U-01AAPOHchr17

64216672

-C1Schr12

7171571

+


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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)
ENST00000205948APOHchr1764216672-ENST00000406697C1Schr127171571+2699642382317759
ENST00000205948APOHchr1764216672-ENST00000328916C1Schr127171571+2699642382317759
ENST00000205948APOHchr1764216672-ENST00000360817C1Schr127171571+2610642382317759

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
ENST00000205948ENST00000406697APOHchr1764216672-C1Schr127171571+0.0001917830.99980825
ENST00000205948ENST00000328916APOHchr1764216672-C1Schr127171571+0.0001917830.99980825
ENST00000205948ENST00000360817APOHchr1764216672-C1Schr127171571+0.0002187580.9997813

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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

>5603_5603_1_APOH-C1S_APOH_chr17_64216672_ENST00000205948_C1S_chr12_7171571_ENST00000328916_length(amino acids)=759AA_BP=201
MISPVLILFSSFLCHVAIAGRTCPKPDDLPFSTVVPLKTFYEPGEEITYSCKPGYVSRGGMRKFICPLTGLWPINTLKCTPRVCPFAGIL
ENGAVRYTTFEYPNTISFSCNTGFYLNGADSAKCTEEGKWSPELPVCAPIICPPPSIPTFATLRVYKPSAGNNSLYRDTAVFECLPQHAM
FGNDTITCTTHGNWTKLPECRDINECTDFVDVPCSHFCNNFIGGYFCSCPPEYFLHDDMKNCGVNCSGDVFTALIGEIASPNYPKPYPEN
SRCEYQIRLEKGFQVVVTLRREDFDVEAADSAGNCLDSLVFVAGDRQFGPYCGHGFPGPLNIETKSNALDIIFQTDLTGQKKGWKLRYHG
DPMPCPKEDTPNSVWEPAKAKYVFRDVVQITCLDGFEVVEGRVGATSFYSTCQSNGKWSNSKLKCQPVDCGIPESIENGKVEDPESTLFG
SVIRYTCEEPYYYMENGGGGEYHCAGNGSWVNEVLGPELPKCVPVCGVPREPFEEKQRIIGGSDADIKNFPWQVFFDNPWAGGALINEYW
VLTAAHVVEGNREPTMYVGSTSVQTSRLAKSKMLTPEHVFIHPGWKLLEVPEGRTNFDNDIALVRLKDPVKMGPTVSPICLPGTSSDYNL
MDGDLGLISGWGRTEKRDRAVRLKAARLPVAPLRKCKEVKVEKPTADAEAYVFTPNMICAGGEKGMDSCKGDSGGAFAVQDPNDKTKFYA

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

>5603_5603_2_APOH-C1S_APOH_chr17_64216672_ENST00000205948_C1S_chr12_7171571_ENST00000360817_length(amino acids)=759AA_BP=201
MISPVLILFSSFLCHVAIAGRTCPKPDDLPFSTVVPLKTFYEPGEEITYSCKPGYVSRGGMRKFICPLTGLWPINTLKCTPRVCPFAGIL
ENGAVRYTTFEYPNTISFSCNTGFYLNGADSAKCTEEGKWSPELPVCAPIICPPPSIPTFATLRVYKPSAGNNSLYRDTAVFECLPQHAM
FGNDTITCTTHGNWTKLPECRDINECTDFVDVPCSHFCNNFIGGYFCSCPPEYFLHDDMKNCGVNCSGDVFTALIGEIASPNYPKPYPEN
SRCEYQIRLEKGFQVVVTLRREDFDVEAADSAGNCLDSLVFVAGDRQFGPYCGHGFPGPLNIETKSNALDIIFQTDLTGQKKGWKLRYHG
DPMPCPKEDTPNSVWEPAKAKYVFRDVVQITCLDGFEVVEGRVGATSFYSTCQSNGKWSNSKLKCQPVDCGIPESIENGKVEDPESTLFG
SVIRYTCEEPYYYMENGGGGEYHCAGNGSWVNEVLGPELPKCVPVCGVPREPFEEKQRIIGGSDADIKNFPWQVFFDNPWAGGALINEYW
VLTAAHVVEGNREPTMYVGSTSVQTSRLAKSKMLTPEHVFIHPGWKLLEVPEGRTNFDNDIALVRLKDPVKMGPTVSPICLPGTSSDYNL
MDGDLGLISGWGRTEKRDRAVRLKAARLPVAPLRKCKEVKVEKPTADAEAYVFTPNMICAGGEKGMDSCKGDSGGAFAVQDPNDKTKFYA

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

>5603_5603_3_APOH-C1S_APOH_chr17_64216672_ENST00000205948_C1S_chr12_7171571_ENST00000406697_length(amino acids)=759AA_BP=201
MISPVLILFSSFLCHVAIAGRTCPKPDDLPFSTVVPLKTFYEPGEEITYSCKPGYVSRGGMRKFICPLTGLWPINTLKCTPRVCPFAGIL
ENGAVRYTTFEYPNTISFSCNTGFYLNGADSAKCTEEGKWSPELPVCAPIICPPPSIPTFATLRVYKPSAGNNSLYRDTAVFECLPQHAM
FGNDTITCTTHGNWTKLPECRDINECTDFVDVPCSHFCNNFIGGYFCSCPPEYFLHDDMKNCGVNCSGDVFTALIGEIASPNYPKPYPEN
SRCEYQIRLEKGFQVVVTLRREDFDVEAADSAGNCLDSLVFVAGDRQFGPYCGHGFPGPLNIETKSNALDIIFQTDLTGQKKGWKLRYHG
DPMPCPKEDTPNSVWEPAKAKYVFRDVVQITCLDGFEVVEGRVGATSFYSTCQSNGKWSNSKLKCQPVDCGIPESIENGKVEDPESTLFG
SVIRYTCEEPYYYMENGGGGEYHCAGNGSWVNEVLGPELPKCVPVCGVPREPFEEKQRIIGGSDADIKNFPWQVFFDNPWAGGALINEYW
VLTAAHVVEGNREPTMYVGSTSVQTSRLAKSKMLTPEHVFIHPGWKLLEVPEGRTNFDNDIALVRLKDPVKMGPTVSPICLPGTSSDYNL
MDGDLGLISGWGRTEKRDRAVRLKAARLPVAPLRKCKEVKVEKPTADAEAYVFTPNMICAGGEKGMDSCKGDSGGAFAVQDPNDKTKFYA

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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/chr17:64216672/chr12:7171571)
- 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
APOH

P02749

C1S

P09871

FUNCTION: Binds to various kinds of negatively charged substances such as heparin, phospholipids, and dextran sulfate. May prevent activation of the intrinsic blood coagulation cascade by binding to phospholipids on the surface of damaged cells.FUNCTION: C1s B chain is a serine protease that combines with C1q and C1r to form C1, the first component of the classical pathway of the complement system. C1r activates C1s so that it can, in turn, activate C2 and C4.

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
HgeneAPOHchr17:64216672chr12:7171571ENST00000205948-58140_202201.33333333333334346.0DomainSushi 3
HgeneAPOHchr17:64216672chr12:7171571ENST00000205948-5821_81201.33333333333334346.0DomainSushi 1
HgeneAPOHchr17:64216672chr12:7171571ENST00000205948-5882_139201.33333333333334346.0DomainSushi 2
TgeneC1Schr17:64216672chr12:7171571ENST00000328916312131_172130.33333333333334689.0DomainNote=EGF-like%3B calcium-binding
TgeneC1Schr17:64216672chr12:7171571ENST00000328916312175_290130.33333333333334689.0DomainCUB 2
TgeneC1Schr17:64216672chr12:7171571ENST00000328916312292_356130.33333333333334689.0DomainSushi 1
TgeneC1Schr17:64216672chr12:7171571ENST00000328916312357_423130.33333333333334689.0DomainSushi 2
TgeneC1Schr17:64216672chr12:7171571ENST00000328916312438_680130.33333333333334689.0DomainPeptidase S1
TgeneC1Schr17:64216672chr12:7171571ENST00000360817312131_172130.33333333333334689.0DomainNote=EGF-like%3B calcium-binding
TgeneC1Schr17:64216672chr12:7171571ENST00000360817312175_290130.33333333333334689.0DomainCUB 2
TgeneC1Schr17:64216672chr12:7171571ENST00000360817312292_356130.33333333333334689.0DomainSushi 1
TgeneC1Schr17:64216672chr12:7171571ENST00000360817312357_423130.33333333333334689.0DomainSushi 2
TgeneC1Schr17:64216672chr12:7171571ENST00000360817312438_680130.33333333333334689.0DomainPeptidase S1
TgeneC1Schr17:64216672chr12:7171571ENST00000406697615131_172130.33333333333334689.0DomainNote=EGF-like%3B calcium-binding
TgeneC1Schr17:64216672chr12:7171571ENST00000406697615175_290130.33333333333334689.0DomainCUB 2
TgeneC1Schr17:64216672chr12:7171571ENST00000406697615292_356130.33333333333334689.0DomainSushi 1
TgeneC1Schr17:64216672chr12:7171571ENST00000406697615357_423130.33333333333334689.0DomainSushi 2
TgeneC1Schr17:64216672chr12:7171571ENST00000406697615438_680130.33333333333334689.0DomainPeptidase S1

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneAPOHchr17:64216672chr12:7171571ENST00000205948-58203_262201.33333333333334346.0DomainSushi 4
HgeneAPOHchr17:64216672chr12:7171571ENST00000205948-58263_345201.33333333333334346.0RegionNote=Sushi-like
TgeneC1Schr17:64216672chr12:7171571ENST0000032891631216_130130.33333333333334689.0DomainCUB 1
TgeneC1Schr17:64216672chr12:7171571ENST0000036081731216_130130.33333333333334689.0DomainCUB 1
TgeneC1Schr17:64216672chr12:7171571ENST0000040669761516_130130.33333333333334689.0DomainCUB 1


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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
APOH
C1S


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 APOH-C1S


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 APOH-C1S


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