UTHEALTH HOME    ABOUT SBMI    A-Z    WEBMAIL    INSIDE THE UNIVERSITY
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine level1
leaf

Fusion Gene Summary

leaf

Fusion Gene Sample Information

leaf

Fusion ORF Analysis

leaf

Fusion Amino Acid Sequences

leaf

Fusion Protein Functional Features

leaf

Fusion Protein-Protein Interaction

leaf

Related drugs with this fusion protein

leaf

Related disease with this fusion protein

Fusion Protein:TCF3-OAZ1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TCF3-OAZ1
FusionPDB ID: 89774
FusionGDB2.0 ID: 89774
HgeneTgene
Gene symbol

TCF3

OAZ1

Gene ID

83439

4946

Gene nametranscription factor 7 like 1ornithine decarboxylase antizyme 1
SynonymsTCF-3|TCF3AZ1|AZI|OAZ
Cytomap

2p11.2

19p13.3

Type of geneprotein-codingprotein-coding
Descriptiontranscription factor 7-like 1HMG box transcription factor 3transcription factor 7-like 1 (T-cell specific, HMG-box)ornithine decarboxylase antizyme 1ODC-Azantizyme 1
Modification date2020031320200313
UniProtAcc

TFPT

.
Ensembl transtripts involved in fusion geneENST idsENST00000262965, ENST00000344749, 
ENST00000395423, ENST00000588136, 
ENST00000453954, 
ENST00000588673, 
ENST00000322297, ENST00000582888, 
ENST00000583542, ENST00000602676, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score21 X 26 X 9=491414 X 9 X 8=1008
# samples 2715
** MAII scorelog2(27/4914*10)=-4.18586654531133
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/1008*10)=-2.74846123300404
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: TCF3 [Title/Abstract] AND OAZ1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TCF3(1646354)-OAZ1(2271384), # samples:1
Anticipated loss of major functional domain due to fusion event.TCF3-OAZ1 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.
TCF3-OAZ1 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.
TCF3-OAZ1 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.
TCF3-OAZ1 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.
TCF3-OAZ1 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
TCF3-OAZ1 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
TCF3-OAZ1 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
TCF3-OAZ1 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
TCF3-OAZ1 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
TgeneOAZ1

GO:0045732

positive regulation of protein catabolic process

17900240


check buttonFusion gene breakpoints across TCF3 (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 OAZ1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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
ChimerDB4BRCATCGA-GM-A2DF-01ATCF3chr19

1646354

-OAZ1chr19

2271384

+


Top

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)
ENST00000344749TCF3chr191646354-ENST00000582888OAZ1chr192271384+972212282746154
ENST00000344749TCF3chr191646354-ENST00000602676OAZ1chr192271384+1133212288752154
ENST00000344749TCF3chr191646354-ENST00000322297OAZ1chr192271384+1130212285749154
ENST00000344749TCF3chr191646354-ENST00000583542OAZ1chr192271384+1157212288776162
ENST00000262965TCF3chr191646354-ENST00000582888OAZ1chr192271384+12504905922197
ENST00000262965TCF3chr191646354-ENST00000602676OAZ1chr192271384+14114904760159
ENST00000262965TCF3chr191646354-ENST00000322297OAZ1chr192271384+14084904760159
ENST00000262965TCF3chr191646354-ENST00000583542OAZ1chr192271384+14354905661054162
ENST00000395423TCF3chr191646354-ENST00000588673OAZ1chr192271384+78117328714228

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
ENST00000344749ENST00000582888TCF3chr191646354-OAZ1chr192271384+0.81176460.18823543
ENST00000344749ENST00000602676TCF3chr191646354-OAZ1chr192271384+0.791501940.20849814
ENST00000344749ENST00000322297TCF3chr191646354-OAZ1chr192271384+0.787502650.21249738
ENST00000344749ENST00000583542TCF3chr191646354-OAZ1chr192271384+0.75908070.24091925
ENST00000262965ENST00000582888TCF3chr191646354-OAZ1chr192271384+0.72895650.27104345
ENST00000262965ENST00000602676TCF3chr191646354-OAZ1chr192271384+0.76246060.23753941
ENST00000262965ENST00000322297TCF3chr191646354-OAZ1chr192271384+0.83038450.16961548
ENST00000262965ENST00000583542TCF3chr191646354-OAZ1chr192271384+0.677369530.3226305
ENST00000395423ENST00000588673TCF3chr191646354-OAZ1chr192271384+0.0202545970.97974545

Top

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

>89774_89774_1_TCF3-OAZ1_TCF3_chr19_1646354_ENST00000262965_OAZ1_chr19_2271384_ENST00000322297_length(amino acids)=159AA_BP=61
MRPGQGGGPALPVGDRQREHHAEVQEVTELLVCAHRRHPLRLVHSPGARAGTSGLETLLGAAGHAARGGGRRHEAGGPPPGQRCVAAGPP

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

>89774_89774_2_TCF3-OAZ1_TCF3_chr19_1646354_ENST00000262965_OAZ1_chr19_2271384_ENST00000582888_length(amino acids)=197AA_BP=1
MTIPSPTWDLQGWVRGIGAPPRPRTRVTTAVEGDPEPPNCAPAREAGRPFPLVTGSGNIMLKSRRSLSSLSVPTGAILCGWFILLGPGRA
PQAWKPCWARPGTRRVGGGGGMKRGGPPPDKGASRPGPRGSRVGGGGGARGPGPSHPRVARPAGPVRAAGRGAPGAAACAVPAVPAAASA

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

>89774_89774_3_TCF3-OAZ1_TCF3_chr19_1646354_ENST00000262965_OAZ1_chr19_2271384_ENST00000583542_length(amino acids)=162AA_BP=
MKIPGGRGNSQRDHNLSANLFYSDDRLNVTEELTSNDKTRILNVQSRLTDAKRINWRTVLSGGSLYIEIPGGALPEGSKDSRDADTRCSF

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

>89774_89774_4_TCF3-OAZ1_TCF3_chr19_1646354_ENST00000262965_OAZ1_chr19_2271384_ENST00000602676_length(amino acids)=159AA_BP=61
MRPGQGGGPALPVGDRQREHHAEVQEVTELLVCAHRRHPLRLVHSPGARAGTSGLETLLGAAGHAARGGGRRHEAGGPPPGQRCVAAGPP

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

>89774_89774_5_TCF3-OAZ1_TCF3_chr19_1646354_ENST00000344749_OAZ1_chr19_2271384_ENST00000322297_length(amino acids)=154AA_BP=
MKIPGGRGNSQRDHNLSANLFYSDDRLNVTEELTSNDKTRILNVQSRLTDAKRINWRTVLSGGSLYIEIPGGALPEGSKDSFAVLLEFAE

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

>89774_89774_6_TCF3-OAZ1_TCF3_chr19_1646354_ENST00000344749_OAZ1_chr19_2271384_ENST00000582888_length(amino acids)=154AA_BP=
MKIPGGRGNSQRDHNLSANLFYSDDRLNVTEELTSNDKTRILNVQSRLTDAKRINWRTVLSGGSLYIEIPGGALPEGSKDSFAVLLEFAE

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

>89774_89774_7_TCF3-OAZ1_TCF3_chr19_1646354_ENST00000344749_OAZ1_chr19_2271384_ENST00000583542_length(amino acids)=162AA_BP=
MKIPGGRGNSQRDHNLSANLFYSDDRLNVTEELTSNDKTRILNVQSRLTDAKRINWRTVLSGGSLYIEIPGGALPEGSKDSRDADTRCSF

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

>89774_89774_8_TCF3-OAZ1_TCF3_chr19_1646354_ENST00000344749_OAZ1_chr19_2271384_ENST00000602676_length(amino acids)=154AA_BP=
MKIPGGRGNSQRDHNLSANLFYSDDRLNVTEELTSNDKTRILNVQSRLTDAKRINWRTVLSGGSLYIEIPGGALPEGSKDSFAVLLEFAE

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

>89774_89774_9_TCF3-OAZ1_TCF3_chr19_1646354_ENST00000395423_OAZ1_chr19_2271384_ENST00000588673_length(amino acids)=228AA_BP=47
MNQPQRMAPVGTDKELSDLLDFSMMFPLPVTNGKGRPASLAGAQFGGSVPGSPSTAVVTRVRGLGGAPDAPHPPLKIPGGRGNSQRDHNL
SANLFYSDDRLNVTEELTSNDKTRILNVQSRLTDAKRINWRTVLSGGSLYIEIPGGALPEGSKDSFAVLLEFAEEQLRADHVFICFHKNR

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

Top

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/chr19:1646354/chr19:2271384)
- 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
TCF3

TFPT

.
253FUNCTION: 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
HgeneTCF3chr19:1646354chr19:2271384ENST00000262965-31919_2748.333333333333336655.0MotifNote=9aaTAD
HgeneTCF3chr19:1646354chr19:2271384ENST00000344749-31919_2748.333333333333336652.0MotifNote=9aaTAD
HgeneTCF3chr19:1646354chr19:2271384ENST00000588136-21919_2748.333333333333336527.0MotifNote=9aaTAD

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneTCF3chr19:1646354chr19:2271384ENST00000262965-319549_60248.333333333333336655.0DomainbHLH
HgeneTCF3chr19:1646354chr19:2271384ENST00000344749-319549_60248.333333333333336652.0DomainbHLH
HgeneTCF3chr19:1646354chr19:2271384ENST00000588136-219549_60248.333333333333336527.0DomainbHLH
HgeneTCF3chr19:1646354chr19:2271384ENST00000262965-319170_17648.333333333333336655.0MotifNuclear localization signal
HgeneTCF3chr19:1646354chr19:2271384ENST00000344749-319170_17648.333333333333336652.0MotifNuclear localization signal
HgeneTCF3chr19:1646354chr19:2271384ENST00000588136-219170_17648.333333333333336527.0MotifNuclear localization signal
HgeneTCF3chr19:1646354chr19:2271384ENST00000262965-319389_42548.333333333333336655.0RegionNote=Leucine-zipper
HgeneTCF3chr19:1646354chr19:2271384ENST00000344749-319389_42548.333333333333336652.0RegionNote=Leucine-zipper
HgeneTCF3chr19:1646354chr19:2271384ENST00000588136-219389_42548.333333333333336527.0RegionNote=Leucine-zipper


Top

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
TCF3HAND2, ID3, SKP2, NHLH1, TCF3, EP300, CREBBP, KAT2B, CALM1, LMX1A, TAL1, LDB1, CBFA2T3, ELK3, MYOD1, ID1, ID2, MYF5, MYF6, MYOG, UBE2I, LYL1, MAPKAPK3, TWIST1, DAXX, MEN1, TCF4, RUNX1T1, RUNX1, TRIM33, INO80E, YY1, RB1, ASB2, SOX2, ELAVL1, ID4, KDM1A, PRMT5, MRPL37, RPL23A, UQCRC2, MRPL49, DDX17, SAFB, EIF5A, MYO1B, GSE1, SLC25A10, BHLHA15, PIP, ALDH18A1, SF3A3, DNAJC10, RPL36A, IMMT, RPS13, DDX20, TET2, PRPF8, RCOR1, TCF24, RPL14, PON2, SSBP1, RPL31, MRPL44, C14orf166, SPIN1, CCT2, MYL6B, CHCHD3, ATP2A3, LANCL2, SLC9A3R1, TIMM50, ERLIN2, MRPL39, ATOH8, SERPINH1, SETSIP, SON, FBL, SLC25A4, EEF1A2, LGALS7, C1QBP, CPD, MRPL23, NHLH2, RPL13, COX7A2, CSTA, PCBP1, NDUFB4, TFF3, FLG2, HNRNPR, ERAL1, RPN2, RBM39, RPL24, LBR, CASP14, STK38, CANX, TCF12, FOXH1, Ube2i, TLE1, KAT2A, TRRAP, SUPT3H, TADA2A, Myod1, Tfap4, Tcf12, Scx, Twist2, Usf1, Rpa1, Ncl, USF1, SCX, TCF21, RPL37, MAPKAPK2, RNF14, FAM115A, PTF1A, Crebbp, HAND1, NEUROD1, MESP2, Bhlhe40, BHLHE40, PARP1, Tcf15, Tcf3, PSMD4, NEDD9, XPO1, BCOR, KIF18A, Id2, Kif13b, Dctn3, ATOH1, FERD3L, NEUROG3, FKBP9, COLGALT2, HNRNPL, EGLN3, OLIG1, OLIG2, IRF2BP2, ASCL1, Neurod1, Neurog1, Neurog2, Ascl1, TRAPPC2L, KHSRP, CARM1, HMGCR, NPRL3, TBL1XR1, VPS45, VPS51, RABGEF1, TRAPPC13, CUL5, TRAPPC2, NPRL2, TRAPPC9, POLE3, B3GNT2, ARL5A, SLC30A5, SAR1A, MOGS, RICTOR, HNRNPD, B4GALT3, SEC23IP, CAND1, CBL, MAN1B1, GCNT2, CTBP1, MAN2A1, TRAPPC12, SEC31A, HIST1H4A, APEX1, GLIS1, AURKA, DACH1, WHSC1L1, ASCL3, TWIST2, nsp5ab, DDX58, NEUROG1, TCF15, TCF23, TAL2, FIGLA, MSGN1, NEUROD4, ASCL4, MSC, USP7,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
TCF3all structure
OAZ1


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


Top

Related Drugs to TCF3-OAZ1


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

Top

Related Diseases to TCF3-OAZ1


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
HgeneTCF3C0006413Burkitt Lymphoma2CTD_human;ORPHANET
HgeneTCF3C0343640African Burkitt's lymphoma2CTD_human
HgeneTCF3C4721444Burkitt Leukemia2CTD_human
HgeneTCF3C0001768Agammaglobulinemia1CTD_human;GENOMICS_ENGLAND
HgeneTCF3C0023452Childhood Acute Lymphoblastic Leukemia1CTD_human
HgeneTCF3C0023453L2 Acute Lymphoblastic Leukemia1CTD_human
HgeneTCF3C0023485Precursor B-Cell Lymphoblastic Leukemia-Lymphoma1CTD_human
HgeneTCF3C0398686Primary immune deficiency disorder1GENOMICS_ENGLAND
HgeneTCF3C1832241Agammaglobulinemia, non-Bruton type1ORPHANET
HgeneTCF3C1844383Recurrent bacterial infection1GENOMICS_ENGLAND
HgeneTCF3C1961102Precursor Cell Lymphoblastic Leukemia Lymphoma1CTD_human
HgeneTCF3C4310786AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT1GENOMICS_ENGLAND