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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:TMEM189-MMP23B

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TMEM189-MMP23B
FusionPDB ID: 91847
FusionGDB2.0 ID: 91847
HgeneTgene
Gene symbol

TMEM189

MMP23B

Gene ID

387521

8510

Gene nametransmembrane protein 189matrix metallopeptidase 23B
SynonymsCarF|KUAMIFR|MIFR-1|MMP22|MMP23A
Cytomap

20q13.13

1p36.33

Type of geneprotein-codingprotein-coding
Descriptiontransmembrane protein 189matrix metalloproteinase-23MMP-21MMP-22MMP-23femalysinmatrix metalloproteinase 22matrix metalloproteinase 23Bmatrix metalloproteinase in the female reproductive tractmatrix metalloproteinase-21
Modification date2020031320200313
UniProtAcc.

O75900

Ensembl transtripts involved in fusion geneENST idsENST00000371650, ENST00000371652, 
ENST00000371656, ENST00000557021, 
ENST00000378675, ENST00000356026, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 9 X 6=3781 X 1 X 1=1
# samples 81
** MAII scorelog2(8/378*10)=-2.24031432933371
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context (manual curation of fusion genes in FusionPDB)

PubMed: TMEM189 [Title/Abstract] AND MMP23B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TMEM189(48744511)-MMP23B(1568566), # samples:1
Anticipated loss of major functional domain due to fusion event.TMEM189-MMP23B 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.
TMEM189-MMP23B 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.
TMEM189-MMP23B seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
TMEM189-MMP23B seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneTMEM189

GO:0008611

ether lipid biosynthetic process

31604315

TgeneMMP23B

GO:0006508

proteolysis

9988691


check buttonFusion gene breakpoints across TMEM189 (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 MMP23B (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
ChimerDB4Non-CancerTCGA-L5-A4OQ-11ATMEM189chr20

48744511

-MMP23Bchr1

1568566

+


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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)
ENST00000557021TMEM189chr2048744511-ENST00000356026MMP23Bchr11568566+16278521101597495
ENST00000371650TMEM189chr2048744511-ENST00000356026MMP23Bchr11568566+1554779461524492
ENST00000371652TMEM189chr2048744511-ENST00000356026MMP23Bchr11568566+1563788461533495
ENST00000371656TMEM189chr2048744511-ENST00000356026MMP23Bchr11568566+1338563971308403

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
ENST00000557021ENST00000356026TMEM189chr2048744511-MMP23Bchr11568566+0.144553070.855447
ENST00000371650ENST00000356026TMEM189chr2048744511-MMP23Bchr11568566+0.172118680.8278813
ENST00000371652ENST00000356026TMEM189chr2048744511-MMP23Bchr11568566+0.146981090.85301894
ENST00000371656ENST00000356026TMEM189chr2048744511-MMP23Bchr11568566+0.149116490.85088354

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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

>91847_91847_1_TMEM189-MMP23B_TMEM189_chr20_48744511_ENST00000371650_MMP23B_chr1_1568566_ENST00000356026_length(amino acids)=492AA_BP=244
MPPPPPAERTGPIGRVAMAGAENWPGQQLELDEDEASCCRWGAQHAGARELAALYSPGKRLQEWCSVILCFSLIAHNLVHLLLLARWEDT
PLVILGVVAGALIADFLSGLVHWGADTWGSVELPIAFIRPFREHHIDPTAITRHDFIETNGDNCLVTLLPLLNMAYKFRTHSPEALEQLY
PWECFVFCLIIFGTFTNQIHKWSHTYFGLPRWVTLLQDWHVILPRKHHRIHHVSPHETYFCITTGFYPINHTDCLVSALHHCFDGPTGEL
AHAFFPPHGGIHFDDSEYWVLGPTRYSWKKGVWLTDLVHVAAHEIGHALGLMHSQHGRALMHLNATLRGWKALSQDELWGLHRLYGCLDR
LFVCASWARRGFCDARRRLMKRLCPSSCDFCYEFPFPTVATTPPPPRTKTRLVPEGRNVTFRCGQKILHKKGKVYWYKDQEPLEFSYPGY

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

>91847_91847_2_TMEM189-MMP23B_TMEM189_chr20_48744511_ENST00000371652_MMP23B_chr1_1568566_ENST00000356026_length(amino acids)=495AA_BP=247
MPPPPPAERTGPIGRVAMAGAENWPGQQLELDEDEASCCRWGAQHAGARELAALYSPGKRLQEWCSVILCFSLIAHNLVHLLLLARWEDT
PLVILGVVAGALIADFLSGLVHWGADTWGSVELPIVGKAFIRPFREHHIDPTAITRHDFIETNGDNCLVTLLPLLNMAYKFRTHSPEALE
QLYPWECFVFCLIIFGTFTNQIHKWSHTYFGLPRWVTLLQDWHVILPRKHHRIHHVSPHETYFCITTGFYPINHTDCLVSALHHCFDGPT
GELAHAFFPPHGGIHFDDSEYWVLGPTRYSWKKGVWLTDLVHVAAHEIGHALGLMHSQHGRALMHLNATLRGWKALSQDELWGLHRLYGC
LDRLFVCASWARRGFCDARRRLMKRLCPSSCDFCYEFPFPTVATTPPPPRTKTRLVPEGRNVTFRCGQKILHKKGKVYWYKDQEPLEFSY

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

>91847_91847_3_TMEM189-MMP23B_TMEM189_chr20_48744511_ENST00000371656_MMP23B_chr1_1568566_ENST00000356026_length(amino acids)=403AA_BP=155
MNERAIAGALIADFLSGLVHWGADTWGSVELPIVGKAFIRPFREHHIDPTAITRHDFIETNGDNCLVTLLPLLNMAYKFRTHSPEALEQL
YPWECFVFCLIIFGTFTNQIHKWSHTYFGLPRWVTLLQDWHVILPRKHHRIHHVSPHETYFCITTGFYPINHTDCLVSALHHCFDGPTGE
LAHAFFPPHGGIHFDDSEYWVLGPTRYSWKKGVWLTDLVHVAAHEIGHALGLMHSQHGRALMHLNATLRGWKALSQDELWGLHRLYGCLD
RLFVCASWARRGFCDARRRLMKRLCPSSCDFCYEFPFPTVATTPPPPRTKTRLVPEGRNVTFRCGQKILHKKGKVYWYKDQEPLEFSYPG

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

>91847_91847_4_TMEM189-MMP23B_TMEM189_chr20_48744511_ENST00000557021_MMP23B_chr1_1568566_ENST00000356026_length(amino acids)=495AA_BP=247
MPPPPPAERTGPIGRVAMAGAENWPGQQLELDEDEASCCRWGAQHAGARELAALYSPGKRLQEWCSVILCFSLIAHNLVHLLLLARWEDT
PLVILGVVAGALIADFLSGLVHWGADTWGSVELPIVGKAFIRPFREHHIDPTAITRHDFIETNGDNCLVTLLPLLNMAYKFRTHSPEALE
QLYPWECFVFCLIIFGTFTNQIHKWSHTYFGLPRWVTLLQDWHVILPRKHHRIHHVSPHETYFCITTGFYPINHTDCLVSALHHCFDGPT
GELAHAFFPPHGGIHFDDSEYWVLGPTRYSWKKGVWLTDLVHVAAHEIGHALGLMHSQHGRALMHLNATLRGWKALSQDELWGLHRLYGC
LDRLFVCASWARRGFCDARRRLMKRLCPSSCDFCYEFPFPTVATTPPPPRTKTRLVPEGRNVTFRCGQKILHKKGKVYWYKDQEPLEFSY

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

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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/chr20:48744511/chr1:1568566)
- 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
.MMP23B

O75900

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: Protease. May regulate the surface expression of some potassium channels by retaining them in the endoplasmic reticulum (By similarity). {ECO:0000250}.

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
HgeneTMEM189chr20:48744511chr1:1568566ENST00000371652-56186_190230.33333333333334271.0MotifHistidine box-1
HgeneTMEM189chr20:48744511chr1:1568566ENST00000371652-56213_217230.33333333333334271.0MotifHistidine box-2
HgeneTMEM189chr20:48744511chr1:1568566ENST00000371652-56161_181230.33333333333334271.0TransmembraneHelical
HgeneTMEM189chr20:48744511chr1:1568566ENST00000371652-5647_67230.33333333333334271.0TransmembraneHelical
HgeneTMEM189chr20:48744511chr1:1568566ENST00000371652-5674_94230.33333333333334271.0TransmembraneHelical
TgeneMMP23Bchr20:48744511chr1:1568566ENST0000035602628295_380142.33333333333334391.0DomainNote=Ig-like C2-type

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneMMP23Bchr20:48744511chr1:1568566ENST00000356026281_19142.33333333333334391.0Topological domainCytoplasmic
TgeneMMP23Bchr20:48744511chr1:1568566ENST000003560262841_390142.33333333333334391.0Topological domainLumenal
TgeneMMP23Bchr20:48744511chr1:1568566ENST000003560262820_40142.33333333333334391.0TransmembraneHelical%3B Signal-anchor for type II membrane protein


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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
TMEM189
MMP23B


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 TMEM189-MMP23B


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 TMEM189-MMP23B


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