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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:TMEM123-MMP7 (FusionGDB2 ID:90963)

Fusion Gene Summary for TMEM123-MMP7

check button Fusion gene summary
Fusion gene informationFusion gene name: TMEM123-MMP7
Fusion gene ID: 90963
HgeneTgene
Gene symbol

TMEM123

MMP7

Gene ID

114908

4316

Gene nametransmembrane protein 123matrix metallopeptidase 7
SynonymsKCT3|PORIMIN|PORMINMMP-7|MPSL1|PUMP-1
Cytomap

11q22.2

11q22.2

Type of geneprotein-codingprotein-coding
DescriptionporiminKCT-3keratinocytes associated transmembrane protein 3pro-oncosis receptor inducing membrane injuryserine/threonine-rich receptormatrilysinmatrinmatrix metallopeptidase 7 (matrilysin, uterine)matrix metalloproteinase 7 (matrilysin, uterine)matrix metalloproteinase-7pump-1 proteaseuterine matrilysinuterine metalloproteinase
Modification date2020031320200329
UniProtAcc.

P09237

Ensembl transtripts involved in fusion geneENST00000361236, ENST00000398136, 
ENST00000532161, ENST00000525577, 
ENST00000260227, 
Fusion gene scores* DoF score16 X 10 X 10=16002 X 3 X 3=18
# samples 273
** MAII scorelog2(27/1600*10)=-2.56704059272389
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TMEM123 [Title/Abstract] AND MMP7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTMEM123(102319543)-MMP7(102395795), # samples:2
Anticipated loss of major functional domain due to fusion event.TMEM123-MMP7 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
HgeneTMEM123

GO:0070267

oncosis

9600958|11481458

TgeneMMP7

GO:0006508

proteolysis

15297466|26482249


check buttonFusion gene breakpoints across TMEM123 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across MMP7 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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-A2-A04P-01ATMEM123chr11

102272270

-MMP7chr11

102391535

-
ChimerDB4OVTCGA-04-1348-01ATMEM123chr11

102319543

-MMP7chr11

102395795

-
ChimerDB4OVTCGA-04-1348-01ATMEM123chr11

102319543

-MMP7chr11

102395795

-


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Fusion Gene ORF analysis for TMEM123-MMP7

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
Frame-shiftENST00000361236ENST00000260227TMEM123chr11

102272270

-MMP7chr11

102391535

-
Frame-shiftENST00000398136ENST00000260227TMEM123chr11

102272270

-MMP7chr11

102391535

-
Frame-shiftENST00000532161ENST00000260227TMEM123chr11

102272270

-MMP7chr11

102391535

-
intron-3CDSENST00000525577ENST00000260227TMEM123chr11

102272270

-MMP7chr11

102391535

-
intron-3CDSENST00000361236ENST00000260227TMEM123chr11

102319543

-MMP7chr11

102395795

-
In-frameENST00000398136ENST00000260227TMEM123chr11

102319543

-MMP7chr11

102395795

-
5UTR-3CDSENST00000532161ENST00000260227TMEM123chr11

102319543

-MMP7chr11

102395795

-
5UTR-3CDSENST00000525577ENST00000260227TMEM123chr11

102319543

-MMP7chr11

102395795

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

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

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Fusion Genomic Features for TMEM123-MMP7


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for TMEM123-MMP7


check button Go to

FGviewer for the breakpoints of chr11:102319543-chr11:102395795

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.MMP7

P09237

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: Degrades casein, gelatins of types I, III, IV, and V, and fibronectin. Activates procollagenase. {ECO:0000269|PubMed:2550050}.

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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneTMEM123chr11:102319543chr11:102395795ENST00000361236-1452_1530190.0Compositional biasNote=Thr-rich
HgeneTMEM123chr11:102319543chr11:102395795ENST00000398136-2552_15352.333333333333336209.0Compositional biasNote=Thr-rich
HgeneTMEM123chr11:102319543chr11:102395795ENST00000361236-14188_2080190.0Topological domainCytoplasmic
HgeneTMEM123chr11:102319543chr11:102395795ENST00000361236-1427_1660190.0Topological domainExtracellular
HgeneTMEM123chr11:102319543chr11:102395795ENST00000398136-25188_20852.333333333333336209.0Topological domainCytoplasmic
HgeneTMEM123chr11:102319543chr11:102395795ENST00000398136-2527_16652.333333333333336209.0Topological domainExtracellular
HgeneTMEM123chr11:102319543chr11:102395795ENST00000361236-14167_1870190.0TransmembraneHelical
HgeneTMEM123chr11:102319543chr11:102395795ENST00000398136-25167_18752.333333333333336209.0TransmembraneHelical
TgeneMMP7chr11:102319543chr11:102395795ENST000002602272685_92161.33333333333334268.0MotifCysteine switch


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Fusion Gene Sequence for TMEM123-MMP7


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for TMEM123-MMP7


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 (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for TMEM123-MMP7


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for TMEM123-MMP7


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMMP7C0000786Spontaneous abortion1CTD_human
TgeneMMP7C0000822Abortion, Tubal1CTD_human
TgeneMMP7C0007102Malignant tumor of colon1CTD_human
TgeneMMP7C0009375Colonic Neoplasms1CTD_human
TgeneMMP7C0024623Malignant neoplasm of stomach1CTD_human
TgeneMMP7C0038356Stomach Neoplasms1CTD_human
TgeneMMP7C0041956Ureteral obstruction1CTD_human
TgeneMMP7C1708349Hereditary Diffuse Gastric Cancer1CTD_human
TgeneMMP7C3830362Early Pregnancy Loss1CTD_human
TgeneMMP7C4552766Miscarriage1CTD_human