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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:MTBP-ABCB7

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MTBP-ABCB7
FusionPDB ID: 55551
FusionGDB2.0 ID: 55551
HgeneTgene
Gene symbol

MTBP

ABCB7

Gene ID

27085

22

Gene nameMDM2 binding proteinATP binding cassette subfamily B member 7
SynonymsMDM2BPABC7|ASAT|Atm1p|EST140535
Cytomap

8q24.12

Xq13.3

Type of geneprotein-codingprotein-coding
Descriptionmdm2-binding proteinMDM2 (mouse double minute 2)-binding protein, 104kDMdm2, transformed 3T3 cell double minute 2, p53 binding protein binding protein, 104kDaATP-binding cassette sub-family B member 7, mitochondrialABC transporter 7 proteinATP-binding cassette transporter 7ATP-binding cassette, sub-family B (MDR/TAP), member 7
Modification date2020031320200320
UniProtAcc

Q96DY7

O75027

Ensembl transtripts involved in fusion geneENST idsENST00000305949, ENST00000519841, 
ENST00000534570, ENST00000253577, 
ENST00000339447, ENST00000373394, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score4 X 3 X 3=364 X 5 X 4=80
# samples 44
** MAII scorelog2(4/36*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/80*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: MTBP [Title/Abstract] AND ABCB7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MTBP(121463562)-ABCB7(74288971), # samples:1
Anticipated loss of major functional domain due to fusion event.MTBP-ABCB7 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.
MTBP-ABCB7 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 MTBP (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 ABCB7 (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
ChimerDB4STADTCGA-BR-A4PE-01AMTBPchr8

121463562

+ABCB7chrX

74288971

-


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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)
ENST00000305949MTBPchr8121463562+ENST00000253577ABCB7chrX74288971-1290470451199384
ENST00000305949MTBPchr8121463562+ENST00000339447ABCB7chrX74288971-1288470451199384
ENST00000305949MTBPchr8121463562+ENST00000373394ABCB7chrX74288971-1286470451199384

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
ENST00000305949ENST00000253577MTBPchr8121463562+ABCB7chrX74288971-0.0006658830.99933404
ENST00000305949ENST00000339447MTBPchr8121463562+ABCB7chrX74288971-0.0006820490.999318
ENST00000305949ENST00000373394MTBPchr8121463562+ABCB7chrX74288971-0.0006868270.99931324

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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

>55551_55551_1_MTBP-ABCB7_MTBP_chr8_121463562_ENST00000305949_ABCB7_chrX_74288971_ENST00000253577_length(amino acids)=384AA_BP=142
MDRYLLLVIWGEGKFPSAASREAEHGPEVSSGEGTENQPDFTAANVYHLLKRSISASINPEDSTFPACSVGGIPGSKKWFFAVQAIYGFY
QFCSSDWQEIHFDTEKDKIEDVLQTNIEECLGAVECFEEEDSNSRESLSLAEKSTIVRLLFRFYEPQKGSIYLAGQNIQDVSLESLRRAV
GVVPQDAVLFHNTIYYNLLYGNISASPEEVYAVAKLAGLHDAILRMPHGYDTQVGERGLKLSGGEKQRVAIARAILKDPPVILYDEATSS
LDSITEETILGAMKDVVKHRTSIFIAHRLSTVVDADEIIVLDQGKVAERGTHHGLLANPHSIYSEMWHTQSSRVQNHDNPKWEAKKENIS

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

>55551_55551_2_MTBP-ABCB7_MTBP_chr8_121463562_ENST00000305949_ABCB7_chrX_74288971_ENST00000339447_length(amino acids)=384AA_BP=142
MDRYLLLVIWGEGKFPSAASREAEHGPEVSSGEGTENQPDFTAANVYHLLKRSISASINPEDSTFPACSVGGIPGSKKWFFAVQAIYGFY
QFCSSDWQEIHFDTEKDKIEDVLQTNIEECLGAVECFEEEDSNSRESLSLAEKSTIVRLLFRFYEPQKGSIYLAGQNIQDVSLESLRRAV
GVVPQDAVLFHNTIYYNLLYGNISASPEEVYAVAKLAGLHDAILRMPHGYDTQVGERGLKLSGGEKQRVAIARAILKDPPVILYDEATSS
LDSITEETILGAMKDVVKHRTSIFIAHRLSTVVDADEIIVLDQGKVAERGTHHGLLANPHSIYSEMWHTQSSRVQNHDNPKWEAKKENIS

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

>55551_55551_3_MTBP-ABCB7_MTBP_chr8_121463562_ENST00000305949_ABCB7_chrX_74288971_ENST00000373394_length(amino acids)=384AA_BP=142
MDRYLLLVIWGEGKFPSAASREAEHGPEVSSGEGTENQPDFTAANVYHLLKRSISASINPEDSTFPACSVGGIPGSKKWFFAVQAIYGFY
QFCSSDWQEIHFDTEKDKIEDVLQTNIEECLGAVECFEEEDSNSRESLSLAEKSTIVRLLFRFYEPQKGSIYLAGQNIQDVSLESLRRAV
GVVPQDAVLFHNTIYYNLLYGNISASPEEVYAVAKLAGLHDAILRMPHGYDTQVGERGLKLSGGEKQRVAIARAILKDPPVILYDEATSS
LDSITEETILGAMKDVVKHRTSIFIAHRLSTVVDADEIIVLDQGKVAERGTHHGLLANPHSIYSEMWHTQSSRVQNHDNPKWEAKKENIS

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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/chr8:121463562/chrX:74288971)
- 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
MTBP

Q96DY7

ABCB7

O75027

FUNCTION: Inhibits cell migration in vitro and suppresses the invasive behavior of tumor cells (By similarity). May play a role in MDM2-dependent p53/TP53 homeostasis in unstressed cells. Inhibits autoubiquitination of MDM2, thereby enhancing MDM2 stability. This promotes MDM2-mediated ubiquitination of p53/TP53 and its subsequent degradation. {ECO:0000250, ECO:0000269|PubMed:15632057}.FUNCTION: Could be involved in the transport of heme from the mitochondria to the cytosol. Plays a central role in the maturation of cytosolic iron-sulfur (Fe/S) cluster-containing proteins. {ECO:0000269|PubMed:10196363}.

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

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneABCB7chr8:121463562chrX:74288971ENST000002535771016140_436510.6666666666667754.0DomainABC transmembrane type-1
TgeneABCB7chr8:121463562chrX:74288971ENST000002535771016472_706510.6666666666667754.0DomainABC transporter
TgeneABCB7chr8:121463562chrX:74288971ENST000003733941016140_436509.6666666666667753.0DomainABC transmembrane type-1
TgeneABCB7chr8:121463562chrX:74288971ENST000003733941016472_706509.6666666666667753.0DomainABC transporter
TgeneABCB7chr8:121463562chrX:74288971ENST000002535771016505_516510.6666666666667754.0Nucleotide bindingATP
TgeneABCB7chr8:121463562chrX:74288971ENST000003733941016505_516509.6666666666667753.0Nucleotide bindingATP
TgeneABCB7chr8:121463562chrX:74288971ENST000002535771016141_161510.6666666666667754.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000002535771016186_206510.6666666666667754.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000002535771016260_280510.6666666666667754.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000002535771016291_311510.6666666666667754.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000002535771016383_403510.6666666666667754.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000002535771016410_430510.6666666666667754.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000003733941016141_161509.6666666666667753.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000003733941016186_206509.6666666666667753.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000003733941016260_280509.6666666666667753.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000003733941016291_311509.6666666666667753.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000003733941016383_403509.6666666666667753.0TransmembraneHelical
TgeneABCB7chr8:121463562chrX:74288971ENST000003733941016410_430509.6666666666667753.0TransmembraneHelical


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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
MTBP
ABCB7


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
HgeneMTBPchr8:121463562chrX:74288971ENST00000305949+422521_904141.66666666666666905.0MDM2


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Related Drugs to MTBP-ABCB7


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 MTBP-ABCB7


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