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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:ST14-ERBB2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ST14-ERBB2
FusionPDB ID: 86906
FusionGDB2.0 ID: 86906
HgeneTgene
Gene symbol

ST14

ERBB2

Gene ID

6768

2064

Gene namesuppression of tumorigenicity 14erb-b2 receptor tyrosine kinase 2
SynonymsARCI11|HAI|MT-SP1|MTSP1|PRSS14|SNC19|TADG15|TMPRSS14CD340|HER-2|HER-2/neu|HER2|MLN 19|NEU|NGL|TKR1
Cytomap

11q24.3

17q12

Type of geneprotein-codingprotein-coding
Descriptionsuppressor of tumorigenicity 14 proteinmembrane-type serine protease 1prostaminserine protease 14serine protease TADG-15suppression of tumorigenicity 14 (colon carcinoma)suppression of tumorigenicity 14 (colon carcinoma, matriptase, epithin)tumor areceptor tyrosine-protein kinase erbB-2c-erb B2/neu proteinherstatinhuman epidermal growth factor receptor 2metastatic lymph node gene 19 proteinneuro/glioblastoma derived oncogene homologneuroblastoma/glioblastoma derived oncogene homologp185erbB2
Modification date2020031320200329
UniProtAcc.

P04626

Ensembl transtripts involved in fusion geneENST idsENST00000278742, ENST00000584888, 
ENST00000269571, ENST00000406381, 
ENST00000445658, ENST00000540042, 
ENST00000540147, ENST00000541774, 
ENST00000584450, ENST00000584601, 
ENST00000578199, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 8 X 8=64034 X 40 X 10=13600
# samples 1643
** MAII scorelog2(16/640*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(43/13600*10)=-4.9831261814356
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: ST14 [Title/Abstract] AND ERBB2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ST14(130059791)-ERBB2(37873573), # samples:1
Anticipated loss of major functional domain due to fusion event.ST14-ERBB2 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.
ST14-ERBB2 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.
ST14-ERBB2 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.
ST14-ERBB2 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.
ST14-ERBB2 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
ST14-ERBB2 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
ST14-ERBB2 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
ST14-ERBB2 seems lost the major protein functional domain in Tgene partner, which is a kinase due to the frame-shifted 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
HgeneST14

GO:0006508

proteolysis

19911255

TgeneERBB2

GO:0007165

signal transduction

10572067

TgeneERBB2

GO:0007166

cell surface receptor signaling pathway

9685399

TgeneERBB2

GO:0007169

transmembrane receptor protein tyrosine kinase signaling pathway

7514177

TgeneERBB2

GO:0014065

phosphatidylinositol 3-kinase signaling

7556068

TgeneERBB2

GO:0018108

peptidyl-tyrosine phosphorylation

12000754

TgeneERBB2

GO:0032886

regulation of microtubule-based process

20937854

TgeneERBB2

GO:0035556

intracellular signal transduction

19372587

TgeneERBB2

GO:0042060

wound healing

12646923

TgeneERBB2

GO:0043406

positive regulation of MAP kinase activity

10572067

TgeneERBB2

GO:0045785

positive regulation of cell adhesion

7556068

TgeneERBB2

GO:0046777

protein autophosphorylation

7556068

TgeneERBB2

GO:0050679

positive regulation of epithelial cell proliferation

10572067

TgeneERBB2

GO:0071363

cellular response to growth factor stimulus

20010870

TgeneERBB2

GO:0090314

positive regulation of protein targeting to membrane

20010870


check buttonFusion gene breakpoints across ST14 (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 ERBB2 (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
ChimerDB4LUADTCGA-44-A4SS-01AST14chr11

130059791

+ERBB2chr17

37873573

+


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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)
ENST00000278742ST14chr11130059791+ENST00000578199ERBB2chr1737873573+1354101690643287

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
ENST00000278742ENST00000578199ST14chr11130059791+ERBB2chr1737873573+0.0113923230.9886077

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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

>86906_86906_1_ST14-ERBB2_ST14_chr11_130059791_ENST00000278742_ERBB2_chr17_37873573_ENST00000578199_length(amino acids)=287AA_BP=
MRDAELRPVVGDDAALAEGRHSRLLVVGAQEWDSAVQQLQRVLHLAGQAYKLSGVGVLVGIHKILICDPHVAIEDLLDTHVPVLQMPHQE
ADPQQDQEEADQHGCQHHPAPRAMLFHLLDVVDWQELHAFLQAIHFLVPGVVLESRAEVLRAPSALAGPIAPHGPRGRSRVSQASSLPAA
GSHGPQGAGRGAQAAGFRAGPARPTGGGALALARSLSLFLFLRLQLRSHTPARPTQVVSGCGLGPPSPPRSPAHLPGSPARPRRPWGRLL

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

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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/chr11:130059791/chr17:37873573)
- 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
.ERBB2

P04626

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: Protein tyrosine kinase that is part of several cell surface receptor complexes, but that apparently needs a coreceptor for ligand binding. Essential component of a neuregulin-receptor complex, although neuregulins do not interact with it alone. GP30 is a potential ligand for this receptor. Regulates outgrowth and stabilization of peripheral microtubules (MTs). Upon ERBB2 activation, the MEMO1-RHOA-DIAPH1 signaling pathway elicits the phosphorylation and thus the inhibition of GSK3B at cell membrane. This prevents the phosphorylation of APC and CLASP2, allowing its association with the cell membrane. In turn, membrane-bound APC allows the localization of MACF1 to the cell membrane, which is required for microtubule capture and stabilization. {ECO:0000305}.; FUNCTION: In the nucleus is involved in transcriptional regulation. Associates with the 5'-TCAAATTC-3' sequence in the PTGS2/COX-2 promoter and activates its transcription. Implicated in transcriptional activation of CDKN1A; the function involves STAT3 and SRC. Involved in the transcription of rRNA genes by RNA Pol I and enhances protein synthesis and cell growth. {ECO:0000269|PubMed:10358079, ECO:0000269|PubMed:15380516, ECO:0000269|PubMed:21555369}.

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
HgeneST14chr11:130059791chr17:37873573ENST00000278742+5191_55199.33333333333334856.0Topological domainCytoplasmic
HgeneST14chr11:130059791chr17:37873573ENST00000278742+51956_76199.33333333333334856.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneERBB2chr11:130059791chr17:37873573ENST000002695711327720_987579.01256.0DomainProtein kinase
TgeneERBB2chr11:130059791chr17:37873573ENST000005417741327720_987564.01241.0DomainProtein kinase
TgeneERBB2chr11:130059791chr17:37873573ENST000002695711327676_689579.01256.0MotifNote=Nuclear localization signal
TgeneERBB2chr11:130059791chr17:37873573ENST000005417741327676_689564.01241.0MotifNote=Nuclear localization signal
TgeneERBB2chr11:130059791chr17:37873573ENST000002695711327726_734579.01256.0Nucleotide bindingATP
TgeneERBB2chr11:130059791chr17:37873573ENST000005417741327726_734564.01241.0Nucleotide bindingATP
TgeneERBB2chr11:130059791chr17:37873573ENST000002695711327676_1255579.01256.0Topological domainCytoplasmic
TgeneERBB2chr11:130059791chr17:37873573ENST000005417741327676_1255564.01241.0Topological domainCytoplasmic
TgeneERBB2chr11:130059791chr17:37873573ENST000002695711327653_675579.01256.0TransmembraneHelical
TgeneERBB2chr11:130059791chr17:37873573ENST000005417741327653_675564.01241.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneST14chr11:130059791chr17:37873573ENST00000278742+519214_334199.33333333333334856.0DomainCUB 1
HgeneST14chr11:130059791chr17:37873573ENST00000278742+519340_447199.33333333333334856.0DomainCUB 2
HgeneST14chr11:130059791chr17:37873573ENST00000278742+519452_487199.33333333333334856.0DomainLDL-receptor class A 1
HgeneST14chr11:130059791chr17:37873573ENST00000278742+519487_524199.33333333333334856.0DomainLDL-receptor class A 2
HgeneST14chr11:130059791chr17:37873573ENST00000278742+519524_560199.33333333333334856.0DomainLDL-receptor class A 3
HgeneST14chr11:130059791chr17:37873573ENST00000278742+519566_603199.33333333333334856.0DomainLDL-receptor class A 4
HgeneST14chr11:130059791chr17:37873573ENST00000278742+519615_854199.33333333333334856.0DomainPeptidase S1
HgeneST14chr11:130059791chr17:37873573ENST00000278742+51986_203199.33333333333334856.0DomainSEA
HgeneST14chr11:130059791chr17:37873573ENST00000278742+51977_855199.33333333333334856.0Topological domainExtracellular
TgeneERBB2chr11:130059791chr17:37873573ENST00000269571132723_652579.01256.0Topological domainExtracellular
TgeneERBB2chr11:130059791chr17:37873573ENST00000541774132723_652564.01241.0Topological domainExtracellular


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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
ST14
ERBB2


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 ST14-ERBB2


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 ST14-ERBB2


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