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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:SH3PXD2A-HTRA1 (FusionGDB2 ID:80933)

Fusion Gene Summary for SH3PXD2A-HTRA1

check button Fusion gene summary
Fusion gene informationFusion gene name: SH3PXD2A-HTRA1
Fusion gene ID: 80933
HgeneTgene
Gene symbol

SH3PXD2A

HTRA1

Gene ID

9644

5654

Gene nameSH3 and PX domains 2AHtrA serine peptidase 1
SynonymsFISH|SH3MD1|TKS5ARMD7|CADASIL2|CARASIL|HtrA|L56|ORF480|PRSS11
Cytomap

10q24.33

10q26.13

Type of geneprotein-codingprotein-coding
DescriptionSH3 and PX domain-containing protein 2ASH3 multiple domains 1adapter protein TKS5adaptor protein TKS5five SH3 domain-containing proteintyrosine kinase substrate with five SH3 domainsserine protease HTRA1IGFBP5-proteasehigh-temperature requirement A serine peptidase 1protease, serine, 11 (IGF binding)
Modification date2020031320200322
UniProtAcc.

Q92743

Ensembl transtripts involved in fusion geneENST00000427662, ENST00000369774, 
ENST00000355946, ENST00000315994, 
ENST00000540321, ENST00000538130, 
ENST00000368984, 
Fusion gene scores* DoF score12 X 20 X 12=28804 X 5 X 4=80
# samples 295
** MAII scorelog2(29/2880*10)=-3.31194400631474
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SH3PXD2A [Title/Abstract] AND HTRA1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSH3PXD2A(105452785)-HTRA1(124248414), # samples:1
Anticipated loss of major functional domain due to fusion event.SH3PXD2A-HTRA1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
HgeneSH3PXD2A

GO:0006801

superoxide metabolic process

19755710


check buttonFusion gene breakpoints across SH3PXD2A (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 HTRA1 (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
ChiTaRS5.0N/AAV734257SH3PXD2Achr10

105452785

-HTRA1chr10

124248414

+


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Fusion Gene ORF analysis for SH3PXD2A-HTRA1

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-shiftENST00000427662ENST00000368984SH3PXD2Achr10

105452785

-HTRA1chr10

124248414

+
In-frameENST00000369774ENST00000368984SH3PXD2Achr10

105452785

-HTRA1chr10

124248414

+
In-frameENST00000355946ENST00000368984SH3PXD2Achr10

105452785

-HTRA1chr10

124248414

+
5UTR-3CDSENST00000315994ENST00000368984SH3PXD2Achr10

105452785

-HTRA1chr10

124248414

+
intron-3CDSENST00000540321ENST00000368984SH3PXD2Achr10

105452785

-HTRA1chr10

124248414

+
intron-3CDSENST00000538130ENST00000368984SH3PXD2Achr10

105452785

-HTRA1chr10

124248414

+
intron-intronENST00000315994ENST00000368984SH3PXD2Achr10

105452814

-HTRA1chr10

105452814

+
intron-intronENST00000355946ENST00000368984SH3PXD2Achr10

105452814

-HTRA1chr10

105452814

+
intron-intronENST00000369774ENST00000368984SH3PXD2Achr10

105452814

-HTRA1chr10

105452814

+
intron-intronENST00000427662ENST00000368984SH3PXD2Achr10

105452814

-HTRA1chr10

105452814

+
intron-intronENST00000538130ENST00000368984SH3PXD2Achr10

105452814

-HTRA1chr10

105452814

+
intron-intronENST00000540321ENST00000368984SH3PXD2Achr10

105452814

-HTRA1chr10

105452814

+

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)
ENST00000369774SH3PXD2Achr10105452785-ENST00000368984HTRA1chr10124248414+22247042021674490
ENST00000355946SH3PXD2Achr10105452785-ENST00000368984HTRA1chr10124248414+2087567651537490

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
ENST00000369774ENST00000368984SH3PXD2Achr10105452785-HTRA1chr10124248414+0.0017246190.9982754
ENST00000355946ENST00000368984SH3PXD2Achr10105452785-HTRA1chr10124248414+0.0013967240.9986033

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Fusion Genomic Features for SH3PXD2A-HTRA1


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)
SH3PXD2Achr10105452785-HTRA1chr10124248417+0.0001950680.9998049
SH3PXD2Achr10105452785-HTRA1chr10124248417+0.0001950680.9998049

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 SH3PXD2A-HTRA1


check button Go to

FGviewer for the breakpoints of chr10:105452785-chr10:124248414

.
- 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
.HTRA1

Q92743

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: Serine protease with a variety of targets, including extracellular matrix proteins such as fibronectin. HTRA1-generated fibronectin fragments further induce synovial cells to up-regulate MMP1 and MMP3 production. May also degrade proteoglycans, such as aggrecan, decorin and fibromodulin. Through cleavage of proteoglycans, may release soluble FGF-glycosaminoglycan complexes that promote the range and intensity of FGF signals in the extracellular space. Regulates the availability of insulin-like growth factors (IGFs) by cleaving IGF-binding proteins. Inhibits signaling mediated by TGF-beta family members. This activity requires the integrity of the catalytic site, although it is unclear whether TGF-beta proteins are themselves degraded. By acting on TGF-beta signaling, may regulate many physiological processes, including retinal angiogenesis and neuronal survival and maturation during development. Intracellularly, degrades TSC2, leading to the activation of TSC2 downstream targets. {ECO:0000269|PubMed:16377621, ECO:0000269|PubMed:20671064, ECO:0000269|PubMed:9852107}.

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
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000355946-6144_128142.333333333333341106.0DomainPX
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000369774-6154_128142.333333333333341134.0DomainPX
TgeneHTRA1chr10:105452785chr10:124248414ENST0000036898409365_467157.33333333333334481.0DomainPDZ
TgeneHTRA1chr10:105452785chr10:124248414ENST0000036898409204_364157.33333333333334481.0RegionNote=Serine protease

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000355946-614917_946142.333333333333341106.0Coiled coilOntology_term=ECO:0000255
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000369774-615917_946142.333333333333341134.0Coiled coilOntology_term=ECO:0000255
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000355946-614634_724142.333333333333341106.0Compositional biasNote=Ser-rich
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000369774-615634_724142.333333333333341134.0Compositional biasNote=Ser-rich
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000355946-6141072_1133142.333333333333341106.0DomainSH3 5
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000355946-614166_225142.333333333333341106.0DomainSH3 1
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000355946-614266_325142.333333333333341106.0DomainSH3 2
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000355946-614448_507142.333333333333341106.0DomainSH3 3
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000355946-614840_899142.333333333333341106.0DomainSH3 4
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000369774-6151072_1133142.333333333333341134.0DomainSH3 5
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000369774-615166_225142.333333333333341134.0DomainSH3 1
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000369774-615266_325142.333333333333341134.0DomainSH3 2
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000369774-615448_507142.333333333333341134.0DomainSH3 3
HgeneSH3PXD2Achr10:105452785chr10:124248414ENST00000369774-615840_899142.333333333333341134.0DomainSH3 4
TgeneHTRA1chr10:105452785chr10:124248414ENST000003689840933_100157.33333333333334481.0DomainIGFBP N-terminal
TgeneHTRA1chr10:105452785chr10:124248414ENST000003689840998_157157.33333333333334481.0DomainKazal-like


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Fusion Gene Sequence for SH3PXD2A-HTRA1


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.
>In-frame_ENST00000369774_ENST00000368984_AV734257_SH3PXD2A_chr10_105452785_-_HTRA1_chr10_124248414_length(transcript)=2224nt_BP=704nt
GCGAGCGGGCGAGCGCAGCGCGGCGGCCGCGCGGGAGTGAAGGGGCGCGCGGCAGGCCGGCGGGGAGTCCCCCGGGGCGCACGGAGCCCG
CGCGCCCTCCGGGACCCTCCCCCGTCCCTGGGCCGGACCTGTGGGCGCCGGGAGTCCGGGCAGCGTTCGGCGCGCCGGGCCGGGGTGGCG
GGCGGCCCCGGGACCCCGGCAGCTGGAGAAGGAGCCGGAGCCCGGCCGGGATGAGAAGGTGACGCCGCCGGGGGCGCCACTCGCTTTGTG
GGGGAAGATGCTCGCCTACTGCGTGCAGGATGCCACCGTGGTGGACGTGGAGAAGCGGAGGAACCCCTCCAAGCACTACGTATACATAAT
CAATGTGACCTGGTCTGACTCCACCTCCCAGACTATCTACCGGAGGTACAGCAAGTTCTTTGACCTGCAGATGCAGCTTTTGGATAAGTT
TCCCATTGAAGGTGGCCAGAAGGACCCCAAGCAAAGGATCATCCCCTTCCTCCCAGGCAAGATCCTCTTCCGCAGAAGCCACATCCGGGA
CGTAGCTGTGAAGAGACTGAAGCCCATCGATGAATACTGCCGGGCACTTGTCCGGCTGCCCCCCCACATCTCACAGTGTGACGAAGTCTT
CCGGTTCTTCGAGGCTCGACCCGAGGATGTCAACCCTCCAAAAGAGGACTATGGCAGTTCCAAGAGGAAATCAGGGCAGGAAGATCCCAA
CAGTTTGCGCCATAAATATAACTTTATCGCGGACGTGGTGGAGAAGATCGCCCCTGCCGTGGTTCATATCGAATTGTTTCGCAAGCTTCC
GTTTTCTAAACGAGAGGTGCCGGTGGCTAGTGGGTCTGGGTTTATTGTGTCGGAAGATGGACTGATCGTGACAAATGCCCACGTGGTGAC
CAACAAGCACCGGGTCAAAGTTGAGCTGAAGAACGGTGCCACTTACGAAGCCAAAATCAAGGATGTGGATGAGAAAGCAGACATCGCACT
CATCAAAATTGACCACCAGGGCAAGCTGCCTGTCCTGCTGCTTGGCCGCTCCTCAGAGCTGCGGCCGGGAGAGTTCGTGGTCGCCATCGG
AAGCCCGTTTTCCCTTCAAAACACAGTCACCACCGGGATCGTGAGCACCACCCAGCGAGGCGGCAAAGAGCTGGGGCTCCGCAACTCAGA
CATGGACTACATCCAGACCGACGCCATCATCAACTATGGAAACTCGGGAGGCCCGTTAGTAAACCTGGACGGTGAAGTGATTGGAATTAA
CACTTTGAAAGTGACAGCTGGAATCTCCTTTGCAATCCCATCTGATAAGATTAAAAAGTTCCTCACGGAGTCCCATGACCGACAGGCCAA
AGGAAAAGCCATCACCAAGAAGAAGTATATTGGTATCCGAATGATGTCACTCACGTCCAGCAAAGCCAAAGAGCTGAAGGACCGGCACCG
GGACTTCCCAGACGTGATCTCAGGAGCGTATATAATTGAAGTAATTCCTGATACCCCAGCAGAAGCTGGTGGTCTCAAGGAAAACGACGT
CATAATCAGCATCAATGGACAGTCCGTGGTCTCCGCCAATGATGTCAGCGACGTCATTAAAAGGGAAAGCACCCTGAACATGGTGGTCCG
CAGGGGTAATGAAGATATCATGATCACAGTGATTCCCGAAGAAATTGACCCATAGGCAGAGGCATGAGCTGGACTTCATGTTTCCCTCAA
AGACTCTCCCGTGGATGACGGATGAGGACTCTGGGCTGCTGGAATAGGACACTCAAGACTTTTGACTGCCATTTTGTTTGTTCAGTGGAG
ACTCCCTGGCCAACAGAATCCTTCTTGATAGTTTGCAGGCAAAACAAATGTAATGTTGCAGATCCGCAGGCAGAAGCTCTGCCCTTCTGT
ATCCTATGTATGCAGTGTGCTTTTTCTTGCCAGCTTGGGCCATTCTTGCTTAGACAGTCAGCATTTGTCTCCTCCTTTAACTGAGTCATC
ATCTTAGTCCAACTAATGCAGTCGATACAATGCGTAGATAGAAGAAGCCCCACGGGAGCCAGGATGGGACTGGTCGTGTTTGTGCTTTTC
TCCAAGTCAGCACCCAAAGGTCAATGCACAGAGACCCCGGGTGGGTGAGCGCTGGCTTCTCAAACGGCCGAAGTTGCCTCTTTTAGGAAT

>In-frame_ENST00000369774_ENST00000368984_AV734257_SH3PXD2A_chr10_105452785_-_HTRA1_chr10_124248414_length(amino acids)=490AA_start in transcript=202_stop in transcript=1674
MEKEPEPGRDEKVTPPGAPLALWGKMLAYCVQDATVVDVEKRRNPSKHYVYIINVTWSDSTSQTIYRRYSKFFDLQMQLLDKFPIEGGQK
DPKQRIIPFLPGKILFRRSHIRDVAVKRLKPIDEYCRALVRLPPHISQCDEVFRFFEARPEDVNPPKEDYGSSKRKSGQEDPNSLRHKYN
FIADVVEKIAPAVVHIELFRKLPFSKREVPVASGSGFIVSEDGLIVTNAHVVTNKHRVKVELKNGATYEAKIKDVDEKADIALIKIDHQG
KLPVLLLGRSSELRPGEFVVAIGSPFSLQNTVTTGIVSTTQRGGKELGLRNSDMDYIQTDAIINYGNSGGPLVNLDGEVIGINTLKVTAG
ISFAIPSDKIKKFLTESHDRQAKGKAITKKKYIGIRMMSLTSSKAKELKDRHRDFPDVISGAYIIEVIPDTPAEAGGLKENDVIISINGQ

--------------------------------------------------------------
>In-frame_ENST00000355946_ENST00000368984_AV734257_SH3PXD2A_chr10_105452785_-_HTRA1_chr10_124248414_length(transcript)=2087nt_BP=567nt
CCGGGAGTCCGGGCAGCGTTCGGCGCGCCGGGCCGGGGTGGCGGGCGGCCCCGGGACCCCGGCAGCTGGAGAAGGAGCCGGAGCCCGGCC
GGGATGAGAAGGTGACGCCGCCGGGGGCGCCACTCGCTTTGTGGGGGAAGATGCTCGCCTACTGCGTGCAGGATGCCACCGTGGTGGACG
TGGAGAAGCGGAGGAACCCCTCCAAGCACTACGTATACATAATCAATGTGACCTGGTCTGACTCCACCTCCCAGACTATCTACCGGAGGT
ACAGCAAGTTCTTTGACCTGCAGATGCAGCTTTTGGATAAGTTTCCCATTGAAGGTGGCCAGAAGGACCCCAAGCAAAGGATCATCCCCT
TCCTCCCAGGCAAGATCCTCTTCCGCAGAAGCCACATCCGGGACGTAGCTGTGAAGAGACTGAAGCCCATCGATGAATACTGCCGGGCAC
TTGTCCGGCTGCCCCCCCACATCTCACAGTGTGACGAAGTCTTCCGGTTCTTCGAGGCTCGACCCGAGGATGTCAACCCTCCAAAAGAGG
ACTATGGCAGTTCCAAGAGGAAATCAGGGCAGGAAGATCCCAACAGTTTGCGCCATAAATATAACTTTATCGCGGACGTGGTGGAGAAGA
TCGCCCCTGCCGTGGTTCATATCGAATTGTTTCGCAAGCTTCCGTTTTCTAAACGAGAGGTGCCGGTGGCTAGTGGGTCTGGGTTTATTG
TGTCGGAAGATGGACTGATCGTGACAAATGCCCACGTGGTGACCAACAAGCACCGGGTCAAAGTTGAGCTGAAGAACGGTGCCACTTACG
AAGCCAAAATCAAGGATGTGGATGAGAAAGCAGACATCGCACTCATCAAAATTGACCACCAGGGCAAGCTGCCTGTCCTGCTGCTTGGCC
GCTCCTCAGAGCTGCGGCCGGGAGAGTTCGTGGTCGCCATCGGAAGCCCGTTTTCCCTTCAAAACACAGTCACCACCGGGATCGTGAGCA
CCACCCAGCGAGGCGGCAAAGAGCTGGGGCTCCGCAACTCAGACATGGACTACATCCAGACCGACGCCATCATCAACTATGGAAACTCGG
GAGGCCCGTTAGTAAACCTGGACGGTGAAGTGATTGGAATTAACACTTTGAAAGTGACAGCTGGAATCTCCTTTGCAATCCCATCTGATA
AGATTAAAAAGTTCCTCACGGAGTCCCATGACCGACAGGCCAAAGGAAAAGCCATCACCAAGAAGAAGTATATTGGTATCCGAATGATGT
CACTCACGTCCAGCAAAGCCAAAGAGCTGAAGGACCGGCACCGGGACTTCCCAGACGTGATCTCAGGAGCGTATATAATTGAAGTAATTC
CTGATACCCCAGCAGAAGCTGGTGGTCTCAAGGAAAACGACGTCATAATCAGCATCAATGGACAGTCCGTGGTCTCCGCCAATGATGTCA
GCGACGTCATTAAAAGGGAAAGCACCCTGAACATGGTGGTCCGCAGGGGTAATGAAGATATCATGATCACAGTGATTCCCGAAGAAATTG
ACCCATAGGCAGAGGCATGAGCTGGACTTCATGTTTCCCTCAAAGACTCTCCCGTGGATGACGGATGAGGACTCTGGGCTGCTGGAATAG
GACACTCAAGACTTTTGACTGCCATTTTGTTTGTTCAGTGGAGACTCCCTGGCCAACAGAATCCTTCTTGATAGTTTGCAGGCAAAACAA
ATGTAATGTTGCAGATCCGCAGGCAGAAGCTCTGCCCTTCTGTATCCTATGTATGCAGTGTGCTTTTTCTTGCCAGCTTGGGCCATTCTT
GCTTAGACAGTCAGCATTTGTCTCCTCCTTTAACTGAGTCATCATCTTAGTCCAACTAATGCAGTCGATACAATGCGTAGATAGAAGAAG
CCCCACGGGAGCCAGGATGGGACTGGTCGTGTTTGTGCTTTTCTCCAAGTCAGCACCCAAAGGTCAATGCACAGAGACCCCGGGTGGGTG
AGCGCTGGCTTCTCAAACGGCCGAAGTTGCCTCTTTTAGGAATCTCTTTGGAATTGGGAGCACGATGACTCTGAGTTTGAGCTATTAAAG

>In-frame_ENST00000355946_ENST00000368984_AV734257_SH3PXD2A_chr10_105452785_-_HTRA1_chr10_124248414_length(amino acids)=490AA_start in transcript=65_stop in transcript=1537
MEKEPEPGRDEKVTPPGAPLALWGKMLAYCVQDATVVDVEKRRNPSKHYVYIINVTWSDSTSQTIYRRYSKFFDLQMQLLDKFPIEGGQK
DPKQRIIPFLPGKILFRRSHIRDVAVKRLKPIDEYCRALVRLPPHISQCDEVFRFFEARPEDVNPPKEDYGSSKRKSGQEDPNSLRHKYN
FIADVVEKIAPAVVHIELFRKLPFSKREVPVASGSGFIVSEDGLIVTNAHVVTNKHRVKVELKNGATYEAKIKDVDEKADIALIKIDHQG
KLPVLLLGRSSELRPGEFVVAIGSPFSLQNTVTTGIVSTTQRGGKELGLRNSDMDYIQTDAIINYGNSGGPLVNLDGEVIGINTLKVTAG
ISFAIPSDKIKKFLTESHDRQAKGKAITKKKYIGIRMMSLTSSKAKELKDRHRDFPDVISGAYIIEVIPDTPAEAGGLKENDVIISINGQ

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

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Fusion Gene PPI Analysis for SH3PXD2A-HTRA1


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 SH3PXD2A-HTRA1


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 SH3PXD2A-HTRA1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSH3PXD2AC0004238Atrial Fibrillation1CTD_human
HgeneSH3PXD2AC0036341Schizophrenia1PSYGENET
HgeneSH3PXD2AC0038454Cerebrovascular accident1CTD_human
HgeneSH3PXD2AC0206729Neurofibrosarcoma1ORPHANET
HgeneSH3PXD2AC0235480Paroxysmal atrial fibrillation1CTD_human
HgeneSH3PXD2AC0751690Malignant Peripheral Nerve Sheath Tumor1ORPHANET
HgeneSH3PXD2AC0751956Acute Cerebrovascular Accidents1CTD_human
HgeneSH3PXD2AC2585653Persistent atrial fibrillation1CTD_human
HgeneSH3PXD2AC3468561familial atrial fibrillation1CTD_human
TgeneHTRA1C1838577Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy7CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneHTRA1C4225211CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 23GENOMICS_ENGLAND;UNIPROT
TgeneHTRA1C0002170Alopecia1GENOMICS_ENGLAND
TgeneHTRA1C0024121Lung Neoplasms1CTD_human
TgeneHTRA1C0158266Intervertebral Disc Degeneration1GENOMICS_ENGLAND
TgeneHTRA1C0206729Neurofibrosarcoma1ORPHANET
TgeneHTRA1C0242379Malignant neoplasm of lung1CTD_human
TgeneHTRA1C0338656Impaired cognition1GENOMICS_ENGLAND
TgeneHTRA1C0497327Dementia1GENOMICS_ENGLAND
TgeneHTRA1C0751690Malignant Peripheral Nerve Sheath Tumor1ORPHANET
TgeneHTRA1C2733158Cerebral Small Vessel Diseases1GENOMICS_ENGLAND