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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:TMPRSS2-CEP89

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TMPRSS2-CEP89
FusionPDB ID: 92372
FusionGDB2.0 ID: 92372
HgeneTgene
Gene symbol

TMPRSS2

CEP89

Gene ID

7113

84902

Gene nametransmembrane serine protease 2centrosomal protein 89
SynonymsPP9284|PRSS10CCDC123|CEP123
Cytomap

21q22.3

19q13.11

Type of geneprotein-codingprotein-coding
Descriptiontransmembrane protease serine 2epitheliasinserine protease 10transmembrane protease, serine 2centrosomal protein of 89 kDacentrosomal protein 123centrosomal protein 89kDacoiled-coil domain containing 123coiled-coil domain-containing protein 123, mitochondrial
Modification date2020031320200313
UniProtAcc

O15393

Q96ST8

Ensembl transtripts involved in fusion geneENST idsENST00000332149, ENST00000398585, 
ENST00000458356, ENST00000497881, 
ENST00000590597, ENST00000591863, 
ENST00000305768, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score40 X 73 X 10=2920011 X 11 X 7=847
# samples 13015
** MAII scorelog2(130/29200*10)=-4.48938484073892
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/847*10)=-2.49739946883632
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: TMPRSS2 [Title/Abstract] AND CEP89 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TMPRSS2(42860320)-CEP89(33406423), # samples:1
TMPRSS2(42860321)-CEP89(33406423), # samples:1
Anticipated loss of major functional domain due to fusion event.TMPRSS2-CEP89 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.
TMPRSS2-CEP89 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.
TMPRSS2-CEP89 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.
TMPRSS2-CEP89 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.
TMPRSS2-CEP89 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
TMPRSS2-CEP89 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
TMPRSS2-CEP89 seems lost the major protein functional domain in Tgene partner, which is a CGC 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
HgeneTMPRSS2

GO:0006508

proteolysis

21068237|24227843

HgeneTMPRSS2

GO:0046598

positive regulation of viral entry into host cell

21068237|24227843


check buttonFusion gene breakpoints across TMPRSS2 (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 CEP89 (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-CD-5798-01ATMPRSS2chr21

42860321

-CEP89chr19

33406423

-
ChimerDB4STADTCGA-CD-5798TMPRSS2chr21

42860320

-CEP89chr19

33406423

-


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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)
ENST00000332149TMPRSS2chr2142860320-ENST00000305768CEP89chr1933406423-17145801351547470
ENST00000398585TMPRSS2chr2142860320-ENST00000305768CEP89chr1933406423-1751617401584514
ENST00000332149TMPRSS2chr2142860321-ENST00000305768CEP89chr1933406423-17145801351547470
ENST00000398585TMPRSS2chr2142860321-ENST00000305768CEP89chr1933406423-1751617401584514

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
ENST00000332149ENST00000305768TMPRSS2chr2142860320-CEP89chr1933406423-0.0078943770.9921056
ENST00000398585ENST00000305768TMPRSS2chr2142860320-CEP89chr1933406423-0.0068850650.9931149
ENST00000332149ENST00000305768TMPRSS2chr2142860321-CEP89chr1933406423-0.0078943770.9921056
ENST00000398585ENST00000305768TMPRSS2chr2142860321-CEP89chr1933406423-0.0068850650.9931149

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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

>92372_92372_1_TMPRSS2-CEP89_TMPRSS2_chr21_42860320_ENST00000332149_CEP89_chr19_33406423_ENST00000305768_length(amino acids)=470AA_BP=148
MALNSGSPPAIGPYYENHGYQPENPYPAQPTVVPTVYEVHPAQYYPSPVPQYAPRVLTQASNPVVCTQPKSPSGTVCTSKTKKALCITLT
LGTFLVGAALAAGLLWKFMGSKCSNSGIECDSSGTCINPSNWCDGVSHCPGGEDENRCVSKLTKQLMLLEAKTHGQEKELAENREQLEIL
RAKCQELKTHSDGKIAVEVHKSIVNELKSQLQKEEEKERAEMEELMEKLTVLQAQKKSLLLEKNSLTEQNKALEAELERAQKINRKSQKK
IEVLKKQVEKAMGNEMSAHQYLANLVGLAENITQERDSLMCLAKCLESEKDGVLNKVIKSNIRLGKLEEKVKGYKKQAALKLGDISHRLL
EQQEDFAGKTAQYRQEMRHLHQVLKDKQEVLDQALQQNREMEGELEVIWESTFRENRRIRELLQDTLTRTGVQDNPRALVAPSLNGVSQA

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

>92372_92372_2_TMPRSS2-CEP89_TMPRSS2_chr21_42860320_ENST00000398585_CEP89_chr19_33406423_ENST00000305768_length(amino acids)=514AA_BP=192
MGAWDPPMPPAPPGGESGCEERGAAGHIEHSRYLSLLDAVDNSKMALNSGSPPAIGPYYENHGYQPENPYPAQPTVVPTVYEVHPAQYYP
SPVPQYAPRVLTQASNPVVCTQPKSPSGTVCTSKTKKALCITLTLGTFLVGAALAAGLLWKFMGSKCSNSGIECDSSGTCINPSNWCDGV
SHCPGGEDENRCVSKLTKQLMLLEAKTHGQEKELAENREQLEILRAKCQELKTHSDGKIAVEVHKSIVNELKSQLQKEEEKERAEMEELM
EKLTVLQAQKKSLLLEKNSLTEQNKALEAELERAQKINRKSQKKIEVLKKQVEKAMGNEMSAHQYLANLVGLAENITQERDSLMCLAKCL
ESEKDGVLNKVIKSNIRLGKLEEKVKGYKKQAALKLGDISHRLLEQQEDFAGKTAQYRQEMRHLHQVLKDKQEVLDQALQQNREMEGELE

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

>92372_92372_3_TMPRSS2-CEP89_TMPRSS2_chr21_42860321_ENST00000332149_CEP89_chr19_33406423_ENST00000305768_length(amino acids)=470AA_BP=148
MALNSGSPPAIGPYYENHGYQPENPYPAQPTVVPTVYEVHPAQYYPSPVPQYAPRVLTQASNPVVCTQPKSPSGTVCTSKTKKALCITLT
LGTFLVGAALAAGLLWKFMGSKCSNSGIECDSSGTCINPSNWCDGVSHCPGGEDENRCVSKLTKQLMLLEAKTHGQEKELAENREQLEIL
RAKCQELKTHSDGKIAVEVHKSIVNELKSQLQKEEEKERAEMEELMEKLTVLQAQKKSLLLEKNSLTEQNKALEAELERAQKINRKSQKK
IEVLKKQVEKAMGNEMSAHQYLANLVGLAENITQERDSLMCLAKCLESEKDGVLNKVIKSNIRLGKLEEKVKGYKKQAALKLGDISHRLL
EQQEDFAGKTAQYRQEMRHLHQVLKDKQEVLDQALQQNREMEGELEVIWESTFRENRRIRELLQDTLTRTGVQDNPRALVAPSLNGVSQA

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

>92372_92372_4_TMPRSS2-CEP89_TMPRSS2_chr21_42860321_ENST00000398585_CEP89_chr19_33406423_ENST00000305768_length(amino acids)=514AA_BP=192
MGAWDPPMPPAPPGGESGCEERGAAGHIEHSRYLSLLDAVDNSKMALNSGSPPAIGPYYENHGYQPENPYPAQPTVVPTVYEVHPAQYYP
SPVPQYAPRVLTQASNPVVCTQPKSPSGTVCTSKTKKALCITLTLGTFLVGAALAAGLLWKFMGSKCSNSGIECDSSGTCINPSNWCDGV
SHCPGGEDENRCVSKLTKQLMLLEAKTHGQEKELAENREQLEILRAKCQELKTHSDGKIAVEVHKSIVNELKSQLQKEEEKERAEMEELM
EKLTVLQAQKKSLLLEKNSLTEQNKALEAELERAQKINRKSQKKIEVLKKQVEKAMGNEMSAHQYLANLVGLAENITQERDSLMCLAKCL
ESEKDGVLNKVIKSNIRLGKLEEKVKGYKKQAALKLGDISHRLLEQQEDFAGKTAQYRQEMRHLHQVLKDKQEVLDQALQQNREMEGELE

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

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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/chr21:42860320/chr19:33406423)
- 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
TMPRSS2

O15393

CEP89

Q96ST8

FUNCTION: Plasma membrane-anchored serine protease that participates in proteolytic cascades of relevance for the normal physiologic function of the prostate (PubMed:25122198). Androgen-induced TMPRSS2 activates several substrates that include pro-hepatocyte growth factor/HGF, the protease activated receptor-2/F2RL1 or matriptase/ST14 leading to extracellular matrix disruption and metastasis of prostate cancer cells (PubMed:15537383, PubMed:26018085, PubMed:25122198). In addition, activates trigeminal neurons and contribute to both spontaneous pain and mechanical allodynia (By similarity). {ECO:0000250|UniProtKB:Q9JIQ8, ECO:0000269|PubMed:15537383, ECO:0000269|PubMed:25122198, ECO:0000269|PubMed:26018085}.; FUNCTION: (Microbial infection) Facilitates human coronaviruses SARS-CoV and SARS-CoV-2 infections via two independent mechanisms, proteolytic cleavage of ACE2 receptor which promotes viral uptake, and cleavage of coronavirus spike glycoproteins which activates the glycoprotein for host cell entry (PubMed:24227843, PubMed:32142651, PubMed:32404436, PubMed:34159616, PubMed:33051876). Upon SARS-CoV-2 infection, increases syncytia formation by accelerating the fusion process (PubMed:34159616, PubMed:33051876). Proteolytically cleaves and activates the spike glycoproteins of human coronavirus 229E (HCoV-229E) and human coronavirus EMC (HCoV-EMC) and the fusion glycoproteins F0 of Sendai virus (SeV), human metapneumovirus (HMPV), human parainfluenza 1, 2, 3, 4a and 4b viruses (HPIV). Essential for spread and pathogenesis of influenza A virus (strains H1N1, H3N2 and H7N9); involved in proteolytic cleavage and activation of hemagglutinin (HA) protein which is essential for viral infectivity. {ECO:0000269|PubMed:21068237, ECO:0000269|PubMed:21325420, ECO:0000269|PubMed:23536651, ECO:0000269|PubMed:23966399, ECO:0000269|PubMed:24027332, ECO:0000269|PubMed:24227843, ECO:0000269|PubMed:32142651, ECO:0000269|PubMed:32404436, ECO:0000269|PubMed:33051876, ECO:0000269|PubMed:34159616}.FUNCTION: Required for ciliogenesis. Also plays a role in mitochondrial metabolism where it may modulate complex IV activity. {ECO:0000269|PubMed:23348840, ECO:0000269|PubMed:23575228}.

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
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000332149-514112_149148.33333333333334493.0DomainLDL-receptor class A
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000398585-514112_149185.33333333333334530.0DomainLDL-receptor class A
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000458356-514112_149148.33333333333334493.0DomainLDL-receptor class A
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000332149-514112_149148.33333333333334493.0DomainLDL-receptor class A
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000398585-514112_149185.33333333333334530.0DomainLDL-receptor class A
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000458356-514112_149148.33333333333334493.0DomainLDL-receptor class A
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000332149-5141_84148.33333333333334493.0Topological domainCytoplasmic
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000398585-5141_84185.33333333333334530.0Topological domainCytoplasmic
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000458356-5141_84148.33333333333334493.0Topological domainCytoplasmic
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000332149-5141_84148.33333333333334493.0Topological domainCytoplasmic
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000398585-5141_84185.33333333333334530.0Topological domainCytoplasmic
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000458356-5141_84148.33333333333334493.0Topological domainCytoplasmic
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000332149-51485_105148.33333333333334493.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000398585-51485_105185.33333333333334530.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000458356-51485_105148.33333333333334493.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000332149-51485_105148.33333333333334493.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000398585-51485_105185.33333333333334530.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000458356-51485_105148.33333333333334493.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneCEP89chr21:42860320chr19:33406423ENST0000059059709234_3330357.0Coiled coilOntology_term=ECO:0000255
TgeneCEP89chr21:42860320chr19:33406423ENST0000059059709369_7190357.0Coiled coilOntology_term=ECO:0000255
TgeneCEP89chr21:42860321chr19:33406423ENST0000059059709234_3330357.0Coiled coilOntology_term=ECO:0000255
TgeneCEP89chr21:42860321chr19:33406423ENST0000059059709369_7190357.0Coiled coilOntology_term=ECO:0000255

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000332149-514150_242148.33333333333334493.0DomainSRCR
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000332149-514256_489148.33333333333334493.0DomainPeptidase S1
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000398585-514150_242185.33333333333334530.0DomainSRCR
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000398585-514256_489185.33333333333334530.0DomainPeptidase S1
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000458356-514150_242148.33333333333334493.0DomainSRCR
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000458356-514256_489148.33333333333334493.0DomainPeptidase S1
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000332149-514150_242148.33333333333334493.0DomainSRCR
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000332149-514256_489148.33333333333334493.0DomainPeptidase S1
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000398585-514150_242185.33333333333334530.0DomainSRCR
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000398585-514256_489185.33333333333334530.0DomainPeptidase S1
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000458356-514150_242148.33333333333334493.0DomainSRCR
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000458356-514256_489148.33333333333334493.0DomainPeptidase S1
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000332149-514106_492148.33333333333334493.0Topological domainExtracellular
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000398585-514106_492185.33333333333334530.0Topological domainExtracellular
HgeneTMPRSS2chr21:42860320chr19:33406423ENST00000458356-514106_492148.33333333333334493.0Topological domainExtracellular
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000332149-514106_492148.33333333333334493.0Topological domainExtracellular
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000398585-514106_492185.33333333333334530.0Topological domainExtracellular
HgeneTMPRSS2chr21:42860321chr19:33406423ENST00000458356-514106_492148.33333333333334493.0Topological domainExtracellular
TgeneCEP89chr21:42860320chr19:33406423ENST000003057681219234_333461.3333333333333784.0Coiled coilOntology_term=ECO:0000255
TgeneCEP89chr21:42860320chr19:33406423ENST000003057681219369_719461.3333333333333784.0Coiled coilOntology_term=ECO:0000255
TgeneCEP89chr21:42860321chr19:33406423ENST000003057681219234_333461.3333333333333784.0Coiled coilOntology_term=ECO:0000255
TgeneCEP89chr21:42860321chr19:33406423ENST000003057681219369_719461.3333333333333784.0Coiled coilOntology_term=ECO:0000255


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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
CEP89LATS2, PICK1, PCM1, CEP162, CEP128, ABLIM1, ANKRD26, ANXA1, ATG2B, CEP131, C3orf14, CC2D1A, CCDC138, CCDC14, CCDC66, CCDC77, CCDC85C, CEP170, CEP192, CEP55, CRK, CSPP1, DHX35, DLG5, FGFR1OP, FLII, GPATCH1, HAUS2, HAUS3, HAUS4, HAUS5, HAUS6, HAUS7, HAUS8, KIAA0753, KIF7, LUZP1, MB21D2, MED4, MPHOSPH9, NCS1, NME7, NMT1, OFD1, PIBF1, PLEKHG1, RNF219, SAMD4B, SIRT2, SRBD1, SSX2IP, TCHP, TP53BP2, TXLNG, UNC45A, WDR83, WRAP73, XRN1, YWHAG, YWHAH, ADSL, C2CD3, CEP164, CEP350, CEP72, ERC1, KIAA1671, KIF14, MAP7D3, MARK2, MOB2, MOB4, NAV1, NPHP4, SDCCAG3, SLC25A12, TBC1D2B, TRIM37, TTK, TXLNA, WDR45, TBC1D31, CNTRL, NINL, MYH9, GAR1, CTDSPL, PTPRG, PMF1, HIF1AN, YWHAE, nsp16, nsp2, HSPA12B, PRKACA, C17orf59, C11orf52, CXADR, DIRAS3, EPB41L4A, FLOT1, GJA1, KRAS, KRT8, LCK, LYN, MLLT4, NDC80, OCLN, PARD3, RAB35, RHOB, STX7, ZFPL1, FXR1, VPS33A, RAP1GDS1, MAGEA9, KCTD18, BRK1, MLLT3, WHAMMP3, ZNF263, YWHAQ, MLLT1, CALCOCO2, TOP1MT, YWHAB,
TMPRSS2CLK1, HNRNPL, DCAF4, S, ACE2, STX7, SCD, PLP2, PLLP, MOSPD3, UPK2, SELK, C3orf52, IGFBP5, SEC22A, PLP1, CLN6, TMEM128, C14orf1, CFHR5, TMEM243, TMEM60, CXCL9, BNIP2, CNIH3, PGAP2, TMEM218, TMEM86A, CMTM7, ZFPL1, BMP10, TMEM79, SLC35A1, SFTPC, VAMP5, FAXDC2, STX8, NINJ2, CLEC7A, C2CD2L, CNIH2, BNIP3, DEFB103A, DEFB103B, TMEM11, C17orf62, TMEM86B, ADIPOQ, EDDM3B, BRICD5, PTTG1IP, PTCH1, ANKRD46, TMEM222, C1QL4, TMEM120B, FAM3C, TMEM229B, PLN, CTXN3, TNF, SMIM1, AQP1, TMPRSS2, DNASE2, MYO1C, PGRMC1, NDUFA4, ADAM10, CLGN, SEC16A, SPINT2, COCH, B4GAT1, XPOT, MYO1B, LANCL1, CALU, PLXNA2, GPC4, BANF1, CPD, CLPX, STC2, SLIT2, MYO1D, ERLIN2, BAG2, TFRC, HLA-A, TP53, RPN1, RPN2, GNAI2, APP, ITGB1, INSR, GLA, GPI, ITGAV, CTSD, APRT, IGF1R, MET, GNAI3, CLTA, CALM2, HLA-C, DLAT, HSPA5, LAMC1, LAMP1, IGF2R, PDIA4, P4HA1, HSP90B1, PVR, RPA2, ATP2A2, PFKL, CDH2, MSH3, RPA1, CALR, RPA3, LONP1, TGFBR1, DDOST, HADHA, ECE1, DNM2, FXR2, PLXNA3, ATP1B3, HADHB, SEC61A1, GNB1, NOMO3, PRKDC, TFAM, SLC7A5, PFKP, KIF23, FMR1, PTK7, ADAM15, CUL2, SCARB2, WRN, DSC3, ITIH4, GANAB, KARS, RCN1, SAFB, IMMT, HSD17B12, UBR4, QSOX2, RRM2B, MON2, YTHDF3, PABPN1, PLD3, PELP1, TTC13, CNNM3, IPO4, FAR1, GGH, ERLEC1, RBM33, DNAJA3, RBM14, PPP1R9B, SDF2, NEU1, GRWD1, AIF1L, NTPCR, FUCA2, EDEM3, RACGAP1, RAB18, TMEM106B, CHPF2, GNG12, DNAJB11, EGFL7, DDX20, ADAMTS1, LNPEP, ITM2B, MRPL11, HYOU1, AFG3L2, YTHDF2, SUPT16H, PDHX, IPO5, SAP18, HGS, SPTBN2, PLXNB2, ARPC3, ACTN4, TRIM13, PDCD6, MPDU1, SEC22B, ATP6AP2, STAM2, ARL6IP5, UFL1, SEC31A, STBD1, SMC2, SEC24A, SEC24B, ACSL3, CDK1, SRPR, SPTB, MTHFD1, ACTN1, ETFA, RAB6A, VDAC1, HMOX2, MYH10, DEK, ATP5C1, NAMPT, VDAC2, QARS, TUFM, SERPINH1, BCAP31, PSMD7, CLCN7, SLC25A1, YARS, EPPK1, RAB10, ABCE1, RHOA, CNBP, TPM4, SLC25A11, LMNB2, CKAP4, GOLGA3, TWF1, TRAP1, STX5, DDX39B, RAB3GAP1, PON2, PPA1, SEC23A, SEC23B, NDUFA9, ATP6V1F, INF2, ANO6, ACTBL2, MIA3, CDKAL1, KIAA0368, C19orf70, SLC25A24, HUWE1, MEGF8, KTN1, COMTD1, ANKLE2, VRK2, ZDHHC17, DNAH10, NUP93, MMGT1, TMEM199, ATPAF2, EMC1, PDZD8, NBEA, MOSPD2, PDCD6IP, SYNE2, UBXN4, CCDC47, LRRC59, C7orf55, DDRGK1, NGLY1, CDK5RAP3, CCDC115, CLCC1, OSBPL9, RBM15, CGRRF1, ESYT1, NDC1, EFHD1, OSBPL8, KIAA1715, LSG1, RAB1B, TMX1, GORASP2, SFXN1, XPO5, VEZT, JPH1, BIRC6, AAAS, TOMM22, DDX19A, SMPD4, TMOD3, EMC3, VAPA, CEP72, LARS, DPM3, DHCR7, UBA2, AASS, ATP6V1H, SLC25A13, STOML2, RAB21, MYO6, VDAC3, AUP1, SEC23IP,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
TMPRSS2all structure
CEP89all structure


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 TMPRSS2-CEP89


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 TMPRSS2-CEP89


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
HgeneTMPRSS2C0033578Prostatic Neoplasms4CTD_human
HgeneTMPRSS2C0376358Malignant neoplasm of prostate4CTD_human