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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:PTPN18-ARID1A

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PTPN18-ARID1A
FusionPDB ID: 70224
FusionGDB2.0 ID: 70224
HgeneTgene
Gene symbol

PTPN18

ARID1A

Gene ID

26469

8289

Gene nameprotein tyrosine phosphatase non-receptor type 18AT-rich interaction domain 1A
SynonymsBDP1|PTP-HSCFB120|BAF250|BAF250a|BM029|C1orf4|CSS2|ELD|MRD14|OSA1|P270|SMARCF1|hELD|hOSA1
Cytomap

2q21.1

1p36.11

Type of geneprotein-codingprotein-coding
Descriptiontyrosine-protein phosphatase non-receptor type 18brain-derived phosphataseprotein tyrosine phosphatase, non-receptor type 18 (brain-derived)AT-rich interactive domain-containing protein 1AARID domain-containing protein 1AAT rich interactive domain 1A (SWI-like)BRG1-associated factor 250aOSA1 nuclear proteinSWI-like proteinSWI/SNF complex protein p270SWI/SNF-related, matrix-associated,
Modification date2020031320200329
UniProtAcc

Q99952

O14497

Ensembl transtripts involved in fusion geneENST idsENST00000420717, ENST00000175756, 
ENST00000347849, 
ENST00000324856, 
ENST00000457599, ENST00000374152, 
ENST00000540690, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score4 X 4 X 2=3213 X 16 X 6=1248
# samples 417
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(17/1248*10)=-2.87601128272455
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: PTPN18 [Title/Abstract] AND ARID1A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PTPN18(131117219)-ARID1A(27056142), # samples:1
Anticipated loss of major functional domain due to fusion event.PTPN18-ARID1A 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.
PTPN18-ARID1A 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.
PTPN18-ARID1A 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.
PTPN18-ARID1A 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
TgeneARID1A

GO:0006337

nucleosome disassembly

8895581

TgeneARID1A

GO:0006338

chromatin remodeling

11726552

TgeneARID1A

GO:0030520

intracellular estrogen receptor signaling pathway

12200431

TgeneARID1A

GO:0030521

androgen receptor signaling pathway

12200431

TgeneARID1A

GO:0042921

glucocorticoid receptor signaling pathway

12200431

TgeneARID1A

GO:0045893

positive regulation of transcription, DNA-templated

12200431


check buttonFusion gene breakpoints across PTPN18 (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 ARID1A (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-BR-7851-11APTPN18chr2

131117219

+ARID1Achr1

27056142

+


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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)
ENST00000175756PTPN18chr2131117219+ENST00000324856ARID1Achr127056142+75845158362352050
ENST00000175756PTPN18chr2131117219+ENST00000457599ARID1Achr127056142+56465158355841833

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
ENST00000175756ENST00000324856PTPN18chr2131117219+ARID1Achr127056142+0.0039650350.9960349
ENST00000175756ENST00000457599PTPN18chr2131117219+ARID1Achr127056142+0.0071879770.992812

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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

>70224_70224_1_PTPN18-ARID1A_PTPN18_chr2_131117219_ENST00000175756_ARID1A_chr1_27056142_ENST00000324856_length(amino acids)=2050AA_BP=144
MLARGAMSRSLDSARSFLERLEARGGREGAVLAGEFSDIQACSAAWKADGVCSTVAGSRPENVRKNRYKDVLPYDQTRVILSLLQEEGHS
DYINGNFIRGVDGSLAYIATQGPLPHTLLDFWRLVWEFGVKVILMACREIENGRPSSPMDQMGKMRPQPYGGTNPYSQQQGPPSGPQQGH
GYPGQPYGSQTPQRYPMTMQGRAQSAMGGLSYTQQIPPYGQQGPSGYGQQGQTPYYNQQSPHPQQQQPPYSQQPPSQTPHAQPSYQQQPQ
SQPPQLQSSQPPYSQQPSQPPHQQSPAPYPSQQSTTQQHPQSQPPYSQPQAQSPYQQQQPQQPAPSTLSQQAAYPQPQSQQSQQTAYSQQ
RFPPPQELSQDSFGSQASSAPSMTSSKGGQEDMNLSLQSRPSSLPDLSGSIDDLPMGTEGALSPGVSTSGISSSQGEQSNPAQSPFSPHT
SPHLPGIRGPSPSPVGSPASVAQSRSGPLSPAAVPGNQMPPRPPSGQSDSIMHPSMNQSSIAQDRGYMQRNPQMPQYSSPQPGSALSPRQ
PSGGQIHTGMGSYQQNSMGSYGPQGGQYGPQGGYPRQPNYNALPNANYPSAGMAGGINPMGAGGQMHGQPGIPPYGTLPPGRMSHASMGN
RPYGPNMANMPPQVGSGMCPPPGGMNRKTQETAVAMHVAANSIQNRPPGYPNMNQGGMMGTGPPYGQGINSMAGMINPQGPPYSMGGTMA
NNSAGMAASPEMMGLGDVKLTPATKMNNKADGTPKTESKSKKSSSSTTTNEKITKLYELGGEPERKMWVDRYLAFTEEKAMGMTNLPAVG
RKPLDLYRLYVSVKEIGGLTQVNKNKKWRELATNLNVGTSSSAASSLKKQYIQCLYAFECKIERGEDPPPDIFAAADSKKSQPKIQPPSP
AGSGSMQGPQTPQSTSSSMAEGGDLKPPTPASTPHSQIPPLPGMSRSNSVGIQDAFNDGSDSTFQKRNSMTPNPGYQPSMNTSDMMGRMS
YEPNKDPYGSMRKAPGSDPFMSSGQGPNGGMGDPYSRAAGPGLGNVAMGPRQHYPYGGPYDRVRTEPGIGPEGNMSTGAPQPNLMPSNPD
SGMYSPSRYPPQQQQQQQQRHDSYGNQFSTQGTPSGSPFPSQQTTMYQQQQQNYKRPMDGTYGPPAKRHEGEMYSVPYSTGQGQPQQQQL
PPAQPQPASQQQAAQPSPQQDVYNQYGNAYPATATAATERRPAGGPQNQFPFQFGRDRVSAPPGTNAQQNMPPQMMGGPIQASAEVAQQG
TMWQGRNDMTYNYANRQSTGSAPQGPAYHGVNRTDEMLHTDQRANHEGSWPSHGTRQPPYGPSAPVPPMTRPPPSNYQPPPSMQNHIPQV
SSPAPLPRPMENRTSPSKSPFLHSGMKMQKAGPPVPASHIAPAPVQPPMIRRDITFPPGSVEATQPVLKQRRRLTMKDIGTPEAWRVMMS
LKSGLLAESTWALDTINILLYDDNSIMTFNLSQLPGLLELLVEYFRRCLIEIFGILKEYEVGDPGQRTLLDPGRFSKVSSPAPMEGGEEE
EELLGPKLEEEEEEEVVENDEEIAFSGKDKPASENSEEKLISKFDKLPVKIVQKNDPFVVDCSDKLGRVQEFDSGLLHWRIGGGDTTEHI
QTHFESKTELLPSRPHAPCPPAPRKHVTTAEGTPGTTDQEGPPPDGPPEKRITATMDDMLSTRSSTLTEDGAKSSEAIKESSKFPFGISP
AQSHRNIKILEDEPHSKDETPLCTLLDWQDSLAKRCVCVSNTIRSLSFVPGNDFEMSKHPGLLLILGKLILLHHKHPERKQAPLTYEKEE
EQDQGVSCNKVEWWWDCLEMLRENTLVTLANISGQLDLSPYPESICLPVLDGLLHWAVCPSAEAQDPFSTLGPNAVLSPQRLVLETLSKL
SIQDNNVDLILATPPFSRLEKLYSTMVRFLSDRKNPVCREMAVVLLANLAQGDSLAARAIAVQKGSIGNLLGFLEDSLAATQFQQSQASL

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

>70224_70224_2_PTPN18-ARID1A_PTPN18_chr2_131117219_ENST00000175756_ARID1A_chr1_27056142_ENST00000457599_length(amino acids)=1833AA_BP=144
MLARGAMSRSLDSARSFLERLEARGGREGAVLAGEFSDIQACSAAWKADGVCSTVAGSRPENVRKNRYKDVLPYDQTRVILSLLQEEGHS
DYINGNFIRGVDGSLAYIATQGPLPHTLLDFWRLVWEFGVKVILMACREIENGRPSSPMDQMGKMRPQPYGGTNPYSQQQGPPSGPQQGH
GYPGQPYGSQTPQRYPMTMQGRAQSAMGGLSYTQQIPPYGQQGPSGYGQQGQTPYYNQQSPHPQQQQPPYSQQPPSQTPHAQPSYQQQPQ
SQPPQLQSSQPPYSQQPSQPPHQQSPAPYPSQQSTTQQHPQSQPPYSQPQAQSPYQQQQPQQPAPSTLSQQAAYPQPQSQQSQQTAYSQQ
RFPPPQELSQDSFGSQASSAPSMTSSKGGQEDMNLSLQSRPSSLPDLSGSIDDLPMGTEGALSPGVSTSGISSSQGEQSNPAQSPFSPHT
SPHLPGIRGPSPSPVGSPASVAQSRSGPLSPAAVPGNQMPPRPPSGQSDSIMHPSMNQSSIAQDRGYMQRNPQMPQYSSPQPGSALSPRQ
PSGGQIHTGMGSYQQNSMGSYGPQGGQYGPQGGYPRQPNYNALPNANYPSAGMAGGINPMGAGGQMHGQPGIPPYGTLPPGRMSHASMGN
RPYGPNMANMPPQVGSGMCPPPGGMNRKTQETAVAMHVAANSIQNRPPGYPNMNQGGMMGTGPPYGQGINSMAGMINPQGPPYSMGGTMA
NNSAGMAASPEMMGLGDVKLTPATKMNNKADGTPKTESKSKKSSSSTTTNEKITKLYELGGEPERKMWVDRYLAFTEEKAMGMTNLPAVG
RKPLDLYRLYVSVKEIGGLTQVNKNKKWRELATNLNVGTSSSAASSLKKQYIQCLYAFECKIERGEDPPPDIFAAADSKKSQPKIQPPSP
AGSGSMQGPQTPQSTSSSMAEGGDLKPPTPASTPHSQIPPLPGMSRSNSVGIQDAFNDGSDSTFQKRNSMTPNPGYQPSMNTSDMMGRMS
YEPNKDPYGSMRKAPGSDPFMSSGQGPNGGMGDPYSRAAGPGLGNVAMGPRQHYPYGGPYDRVRTEPGIGPEGNMSTGAPQPNLMPSNPD
SGMYSPSRYPPQQQQQQQQRHDSYGNQFSTQGTPSGSPFPSQQTTMYQQQQQVSSPAPLPRPMENRTSPSKSPFLHSGMKMQKAGPPVPA
SHIAPAPVQPPMIRRDITFPPGSVEATQPVLKQRRRLTMKDIGTPEAWRVMMSLKSGLLAESTWALDTINILLYDDNSIMTFNLSQLPGL
LELLVEYFRRCLIEIFGILKEYEVGDPGQRTLLDPGRFSKVSSPAPMEGGEEEEELLGPKLEEEEEEEVVENDEEIAFSGKDKPASENSE
EKLISKFDKLPVKIVQKNDPFVVDCSDKLGRVQEFDSGLLHWRIGGGDTTEHIQTHFESKTELLPSRPHAPCPPAPRKHVTTAEGTPGTT
DQEGPPPDGPPEKRITATMDDMLSTRSSTLTEDGAKSSEAIKESSKFPFGISPAQSHRNIKILEDEPHSKDETPLCTLLDWQDSLAKRCV
CVSNTIRSLSFVPGNDFEMSKHPGLLLILGKLILLHHKHPERKQAPLTYEKEEEQDQGVSCNKVEWWWDCLEMLRENTLVTLANISGQLD
LSPYPESICLPVLDGLLHWAVCPSAEAQDPFSTLGPNAVLSPQRLVLETLSKLSIQDNNVDLILATPPFSRLEKLYSTMVRFLSDRKNPV
CREMAVVLLANLAQGDSLAARAIAVQKGSIGNLLGFLEDSLAATQFQQSQASLLHMQNPPFEPTSVDMMRRAARALLALAKVDENHSEFT

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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/chr2:131117219/chr1:27056142)
- 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
PTPN18

Q99952

ARID1A

O14497

FUNCTION: Differentially dephosphorylate autophosphorylated tyrosine kinases which are known to be overexpressed in tumor tissues.FUNCTION: Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Component of SWI/SNF chromatin remodeling complexes that carry out key enzymatic activities, changing chromatin structure by altering DNA-histone contacts within a nucleosome in an ATP-dependent manner. Binds DNA non-specifically. Belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). During neural development a switch from a stem/progenitor to a postmitotic chromatin remodeling mechanism occurs as neurons exit the cell cycle and become committed to their adult state. The transition from proliferating neural stem/progenitor cells to postmitotic neurons requires a switch in subunit composition of the npBAF and nBAF complexes. As neural progenitors exit mitosis and differentiate into neurons, npBAF complexes which contain ACTL6A/BAF53A and PHF10/BAF45A, are exchanged for homologous alternative ACTL6B/BAF53B and DPF1/BAF45B or DPF3/BAF45C subunits in neuron-specific complexes (nBAF). The npBAF complex is essential for the self-renewal/proliferative capacity of the multipotent neural stem cells. The nBAF complex along with CREST plays a role regulating the activity of genes essential for dendrite growth (By similarity). {ECO:0000250|UniProtKB:A2BH40, ECO:0000303|PubMed:12672490, ECO:0000303|PubMed:22952240, ECO:0000303|PubMed:26601204}.

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
TgeneARID1Achr2:131117219chr1:27056142ENST000003248560201327_1404379.02286.0Compositional biasNote=Gln-rich
TgeneARID1Achr2:131117219chr1:27056142ENST00000324856020479_482379.02286.0Compositional biasNote=Poly-Gln
TgeneARID1Achr2:131117219chr1:27056142ENST00000324856020561_567379.02286.0Compositional biasNote=Poly-Gln
TgeneARID1Achr2:131117219chr1:27056142ENST00000324856020998_1001379.02286.0Compositional biasNote=Poly-Ser
TgeneARID1Achr2:131117219chr1:27056142ENST000003741520191327_140401903.0Compositional biasNote=Gln-rich
TgeneARID1Achr2:131117219chr1:27056142ENST00000374152019479_48201903.0Compositional biasNote=Poly-Gln
TgeneARID1Achr2:131117219chr1:27056142ENST00000374152019561_56701903.0Compositional biasNote=Poly-Gln
TgeneARID1Achr2:131117219chr1:27056142ENST00000374152019998_100101903.0Compositional biasNote=Poly-Ser
TgeneARID1Achr2:131117219chr1:27056142ENST000004575990201327_1404379.02069.0Compositional biasNote=Gln-rich
TgeneARID1Achr2:131117219chr1:27056142ENST00000457599020479_482379.02069.0Compositional biasNote=Poly-Gln
TgeneARID1Achr2:131117219chr1:27056142ENST00000457599020561_567379.02069.0Compositional biasNote=Poly-Gln
TgeneARID1Achr2:131117219chr1:27056142ENST00000457599020998_1001379.02069.0Compositional biasNote=Poly-Ser
TgeneARID1Achr2:131117219chr1:27056142ENST000003248560201017_1108379.02286.0DomainARID
TgeneARID1Achr2:131117219chr1:27056142ENST000003741520191017_110801903.0DomainARID
TgeneARID1Achr2:131117219chr1:27056142ENST000004575990201017_1108379.02069.0DomainARID
TgeneARID1Achr2:131117219chr1:27056142ENST000003248560201368_1387379.02286.0MotifNuclear localization signal
TgeneARID1Achr2:131117219chr1:27056142ENST000003248560201709_1713379.02286.0MotifNote=LXXLL
TgeneARID1Achr2:131117219chr1:27056142ENST000003248560201967_1971379.02286.0MotifNote=LXXLL
TgeneARID1Achr2:131117219chr1:27056142ENST000003248560202085_2089379.02286.0MotifNote=LXXLL
TgeneARID1Achr2:131117219chr1:27056142ENST000003741520191368_138701903.0MotifNuclear localization signal
TgeneARID1Achr2:131117219chr1:27056142ENST000003741520191709_171301903.0MotifNote=LXXLL
TgeneARID1Achr2:131117219chr1:27056142ENST000003741520191967_197101903.0MotifNote=LXXLL
TgeneARID1Achr2:131117219chr1:27056142ENST000003741520192085_208901903.0MotifNote=LXXLL
TgeneARID1Achr2:131117219chr1:27056142ENST00000374152019295_29901903.0MotifNote=LXXLL
TgeneARID1Achr2:131117219chr1:27056142ENST000004575990201368_1387379.02069.0MotifNuclear localization signal
TgeneARID1Achr2:131117219chr1:27056142ENST000004575990201709_1713379.02069.0MotifNote=LXXLL
TgeneARID1Achr2:131117219chr1:27056142ENST000004575990201967_1971379.02069.0MotifNote=LXXLL
TgeneARID1Achr2:131117219chr1:27056142ENST000004575990202085_2089379.02069.0MotifNote=LXXLL

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgenePTPN18chr2:131117219chr1:27056142ENST00000175756+51526_291138.0461.0DomainTyrosine-protein phosphatase
HgenePTPN18chr2:131117219chr1:27056142ENST00000347849+11126_2910354.0DomainTyrosine-protein phosphatase
HgenePTPN18chr2:131117219chr1:27056142ENST00000175756+515229_235138.0461.0RegionSubstrate binding
HgenePTPN18chr2:131117219chr1:27056142ENST00000347849+111229_2350354.0RegionSubstrate binding
TgeneARID1Achr2:131117219chr1:27056142ENST00000324856020295_299379.02286.0MotifNote=LXXLL
TgeneARID1Achr2:131117219chr1:27056142ENST00000457599020295_299379.02069.0MotifNote=LXXLL


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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
ARID1AKLF1, GATA1, SMARCB1, SMARCA4, SMARCA2, ING1, SMARCE1, PBRM1, SMARCC2, SMARCC1, PGR, BCL7C, HIC1, CUL2, tat, ARID1B, SMAD2, SMAD3, CARM1, ADNP, RARA, Bcl7b, SOX2, CHD7, SMARCD1, TP53, ELAVL1, SIRT7, TFAP4, CUL3, SMARCD2, ACTL6A, SMARCD3, PHF10, ECT2, YAP1, ITCH, NEDD4, SHMT2, MOV10, NXF1, EED, DPF3, DPF2, SS18, UNK, BCL7A, BCL7B, ESR1, NCOA1, RARB, RARG, EWSR1, Bcl7c, Smarcc1, SNW1, CDC5L, CUL1, SKP1, NFATC1, NFATC2, TOP1, CHEK1, VHL, EYA2, NR3C1, AR, ALDH2, TRIM25, HNRNPL, PDCD6, RMND5A, EZH2, CHD3, CHD4, RUNX1, TNRC6A, RTF1, RBBP7, RUVBL1, MYC, FUS, HIST1H4A, HIST1H2AB, TAF15, DDIT3, FLI1, TP53BP1, BRCA1, MDC1, KIAA1429, ACTC1, ZBTB7A, H2AFX, H2AFY, CTCF, BTRC, WWP2, PLEKHA4, nsp10, ALG13, SMG7, SUPT5H, PRC1, C18orf8, SS18L1, BRD7, DPF1, ARID2, BRD9, GLTSCR1, STK11IP, ASF1A, NUP50, TERF2IP, ATG7, TEX13B, SS18L2, SIRT6, T, ELF5, ERG, ETS1, ETV4, FEV, FOS, FOXI1, GATA2, GATA3, GCM1, HNF1B, HNF4A, IRF1, IRF4, KLF3, KLF4, KLF5, LHX1, LHX2, LHX3, LHX4, MYOD1, NFIA, NFIB, NFIC, NFIX, PAX6, PAX7, PAX8, PAX9, SOX10, SOX15, SOX17, SOX9, SP7, TBR1, TEAD1, TLX1, TLX2, TLX3, BRD3,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
PTPN18
ARID1Aall 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 PTPN18-ARID1A


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 PTPN18-ARID1A


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
TgeneARID1AC0024623Malignant neoplasm of stomach3CTD_human
TgeneARID1AC0038356Stomach Neoplasms3CTD_human
TgeneARID1AC1708349Hereditary Diffuse Gastric Cancer3CTD_human
TgeneARID1AC2239176Liver carcinoma3CTD_human
TgeneARID1AC0033578Prostatic Neoplasms2CTD_human
TgeneARID1AC0376358Malignant neoplasm of prostate2CTD_human
TgeneARID1AC0001418Adenocarcinoma1CTD_human
TgeneARID1AC0005684Malignant neoplasm of urinary bladder1CTD_human
TgeneARID1AC0005695Bladder Neoplasm1CTD_human
TgeneARID1AC0006413Burkitt Lymphoma1CTD_human
TgeneARID1AC0007138Carcinoma, Transitional Cell1CTD_human
TgeneARID1AC0009402Colorectal Carcinoma1CTD_human
TgeneARID1AC0009404Colorectal Neoplasms1CTD_human
TgeneARID1AC0010606Adenoid Cystic Carcinoma1CTD_human
TgeneARID1AC0014170Endometrial Neoplasms1CTD_human
TgeneARID1AC0027708Nephroblastoma1CTD_human
TgeneARID1AC0027819Neuroblastoma1CTD_human
TgeneARID1AC0036920Sezary Syndrome1CTD_human
TgeneARID1AC0079772T-Cell Lymphoma1CTD_human
TgeneARID1AC0079773Lymphoma, T-Cell, Cutaneous1CTD_human
TgeneARID1AC0205641Adenocarcinoma, Basal Cell1CTD_human
TgeneARID1AC0205642Adenocarcinoma, Oxyphilic1CTD_human
TgeneARID1AC0205643Carcinoma, Cribriform1CTD_human
TgeneARID1AC0205644Carcinoma, Granular Cell1CTD_human
TgeneARID1AC0205645Adenocarcinoma, Tubular1CTD_human
TgeneARID1AC0206656Embryonal Rhabdomyosarcoma1CTD_human
TgeneARID1AC0206698Cholangiocarcinoma1CTD_human
TgeneARID1AC0265338Coffin-Siris syndrome1CTD_human;GENOMICS_ENGLAND
TgeneARID1AC0279628Adenocarcinoma Of Esophagus1CTD_human
TgeneARID1AC0343640African Burkitt's lymphoma1CTD_human
TgeneARID1AC0345905Intrahepatic Cholangiocarcinoma1CTD_human
TgeneARID1AC0376407Granulomatous Slack Skin1CTD_human
TgeneARID1AC0476089Endometrial Carcinoma1CTD_human
TgeneARID1AC0920269Microsatellite Instability1CTD_human
TgeneARID1AC1721098Replication Error Phenotype1CTD_human
TgeneARID1AC2930471Bilateral Wilms Tumor1CTD_human
TgeneARID1AC2931822Nasopharyngeal carcinoma1CTD_human
TgeneARID1AC3805278Extrahepatic Cholangiocarcinoma1CTD_human
TgeneARID1AC4721444Burkitt Leukemia1CTD_human