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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:SIPA1L2-NTPCR (FusionGDB2 ID:81948)

Fusion Gene Summary for SIPA1L2-NTPCR

check button Fusion gene summary
Fusion gene informationFusion gene name: SIPA1L2-NTPCR
Fusion gene ID: 81948
HgeneTgene
Gene symbol

SIPA1L2

NTPCR

Gene ID

57568

84284

Gene namesignal induced proliferation associated 1 like 2nucleoside-triphosphatase, cancer-related
SynonymsSPAL2|SPAR2C1orf57|HCR-NTPase|THEP1
Cytomap

1q42.2

1q42.2

Type of geneprotein-codingprotein-coding
Descriptionsignal-induced proliferation-associated 1-like protein 2SIPA1-like protein 2SPA-1-like 2spine-associated RapGAP 2cancer-related nucleoside-triphosphatasehuman cancer-related NTPasenucleoside triphosphate phosphohydrolasenucleoside-triphosphatase C1orf57
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000262861, ENST00000366630, 
ENST00000486472, ENST00000308942, 
ENST00000490098, ENST00000366627, 
ENST00000366628, 
Fusion gene scores* DoF score5 X 5 X 5=1255 X 5 X 4=100
# samples 56
** MAII scorelog2(5/125*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/100*10)=-0.736965594166206
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SIPA1L2 [Title/Abstract] AND NTPCR [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSIPA1L2(232629273)-NTPCR(233113909), # samples:3
Anticipated loss of major functional domain due to fusion event.SIPA1L2-NTPCR seems lost the major protein functional domain in Hgene partner, which is a essential gene 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

check buttonFusion gene breakpoints across SIPA1L2 (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 NTPCR (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4MESOTCGA-SH-A9CU-01ASIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
ChimerDB4MESOTCGA-SH-A9CUSIPA1L2chr1

232629273

-NTPCRchr1

233113909

+


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Fusion Gene ORF analysis for SIPA1L2-NTPCR

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
5CDS-3UTRENST00000262861ENST00000490098SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
5CDS-3UTRENST00000366630ENST00000490098SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
5CDS-intronENST00000262861ENST00000366627SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
5CDS-intronENST00000366630ENST00000366627SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
5UTR-3CDSENST00000486472ENST00000366628SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
5UTR-3UTRENST00000486472ENST00000490098SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
5UTR-intronENST00000486472ENST00000366627SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
Frame-shiftENST00000262861ENST00000366628SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
In-frameENST00000366630ENST00000366628SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
intron-3CDSENST00000308942ENST00000366628SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
intron-3UTRENST00000308942ENST00000490098SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+
intron-intronENST00000308942ENST00000366627SIPA1L2chr1

232629273

-NTPCRchr1

233113909

+

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)
ENST00000366630SIPA1L2chr1232629273-ENST00000366628NTPCRchr1233113909+769619763262044572

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
ENST00000366630ENST00000366628SIPA1L2chr1232629273-NTPCRchr1233113909+0.0003823510.9996176

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Fusion Genomic Features for SIPA1L2-NTPCR


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)
SIPA1L2chr1232629272-NTPCRchr1233113908+0.0002457480.99975425
SIPA1L2chr1232629272-NTPCRchr1233113908+0.0002457480.99975425
SIPA1L2chr1232629272-NTPCRchr1233113908+0.0002457480.99975425
SIPA1L2chr1232629272-NTPCRchr1233113908+0.0002457480.99975425

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.
genomic feature

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.
genomic feature of top 1%

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Fusion Protein Features for SIPA1L2-NTPCR


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/chr1:232629273/chr1:233113909)
- 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
..
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000262861-22160_635391723.0Compositional biasNote=Poly-Gly
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000366630-32260_635391723.0Compositional biasNote=Poly-Gly

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000262861-2211654_17125391723.0Coiled coilOntology_term=ECO:0000255
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000308942-1141654_17120779.0Coiled coilOntology_term=ECO:0000255
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000366630-3221654_17125391723.0Coiled coilOntology_term=ECO:0000255
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000262861-2211125_11285391723.0Compositional biasNote=Poly-Ser
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000262861-2211321_13845391723.0Compositional biasNote=Ser-rich
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000308942-1141125_11280779.0Compositional biasNote=Poly-Ser
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000308942-1141321_13840779.0Compositional biasNote=Ser-rich
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000308942-11460_630779.0Compositional biasNote=Poly-Gly
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000366630-3221125_11285391723.0Compositional biasNote=Poly-Ser
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000366630-3221321_13845391723.0Compositional biasNote=Ser-rich
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000262861-221595_8125391723.0DomainRap-GAP
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000262861-221950_10265391723.0DomainPDZ
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000308942-114595_8120779.0DomainRap-GAP
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000308942-114950_10260779.0DomainPDZ
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000366630-322595_8125391723.0DomainRap-GAP
HgeneSIPA1L2chr1:232629273chr1:233113909ENST00000366630-322950_10265391723.0DomainPDZ
TgeneNTPCRchr1:232629273chr1:233113909ENST0000036662835109_116168191.0Nucleotide bindingATP
TgeneNTPCRchr1:232629273chr1:233113909ENST00000366628359_16168191.0Nucleotide bindingATP


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Fusion Gene Sequence for SIPA1L2-NTPCR


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.
>81948_81948_1_SIPA1L2-NTPCR_SIPA1L2_chr1_232629273_ENST00000366630_NTPCR_chr1_233113909_ENST00000366628_length(transcript)=7696nt_BP=1976nt
ACTAGGGGTGGGCATTGTGTGTGGCTCCCCTGTGGTAGAGAAGGACATCGGATGAACATGTGATCTGTGTATCCAGCTCCAACCCAAAAG
GTGAAGGAAATACTCATGACCAGCCAGATGTCTTAAGGAATGCTTTTGAAAAGAACAGAGGCGTACAACATTATTACGACAACAGAGAAG
CAAGTTGGCTTTGAAGAAACTGTATTCTGAGGATGTTGTTTGCTTTGGGCTAAGAAAAGAAAAAATACAACTACAGACAAAGCCTTTATA
TCTGCAAGTATTATGGCGTGGTCGGTAGCAATGTAATTAGATTTACATCAGTCTTCCTGGTGAGACTTGGAGGCTCTTCCTCGGTAGACA
TGAGTGACCCAAGGCAGTCACAAGAAGAGAAGCACAAGCTAGGCAGAGCCTCTTCAAAGTTCAAGGATCCCCCTAGAATCATGCAGTCAG
ATGATTATTTTGCTCGGAAATTTAAAGCCATTAATGGCAACATGGGACCCACTACTTCTTTAAATGCCTCGAATTCCAATGAGACTGGCG
GTGGTGGTCCGGCTAATGGTACCCCAGCTGTGCCCAAGATGGGTGTGAGAGCAAGGGTGTCTGAATGGCCTCCTAAAAAGGACTGTTCCA
AGGAGCTAACATGCAAGGCACTGTGGGAAAGCCGGTCTCAGACCAGTTATGAAAGCATCACTTCTGTCCTGCAGAATGGGCAGAGTGACC
AGAGTGAAGGTCAGCAAGATGAACAGCTCGATCTGGACTTCGTGGAGGCCAAGTACACAATCGGAGACATCTTTGTCCATTCCCCCCAAA
GAGGACTTCACCCCATAAGACAGAGGAGCAATAGTGATGTCACTATCAGTGACATTGATGCCGAAGATGTCTTAGACCAAAATGCAGTCA
ACCCCAACACCGGGGCTGCCCTGCACAGGGAGTATGGAAGTACTTCATCCATCGACAGGCAAGGCTTATCTGGTGAAAACTTTTTTGCTA
TGCTCAGAGGGTACCGAGTAGAAAATTATGACCACAAAGCAATGGTCCCTTTTGGGTTCCCTGAATTTTTCCGCTGTGACCCTGCAATCT
CTCCGAGCCTTCATGCAGCAGCACAGATTTCTAGGGGAGAATTTGTCCGCATCTCAGGATTAGATTATGTGGACAGTGCCCTCCTGATGG
GGAGAGACAGGGACAAGCCTTTCAAACGGAGGTTGAAATCAGAGTCGGTGGAAACATCTCTCTTCCGAAAGCTTCGAACTGTTAAAAGTG
AGCACGAAACTTTCAAGTTCACGTCTGAGCTGGAGGAGAGCCGACTGGAGAGGGGCATTCGCCCTTGGAATTGTCAGCGATGTTTTGCAC
ATTATGATGTCCAGAGCATTTTGTTTAATATCAACGAAGCCATGGCTACGAGGGCTAATGTGGGGAAAAGGAAAAACATAACCACTGGGG
CATCTGCAGCATCCCAGACTCAGATGCCTACGGGCCAGACAGGCAACTGTGAGTCCCCTTTAGGGAGCAAGGAGGACCTCAACTCCAAAG
AGAACCTGGATGCCGATGAGGGTGATGGGAAAAGTAACGACCTCGTCCTTAGTTGTCCTTACTTTAGAAATGAGACTGGAGGGGAAGGCG
ACAGGCGGATTGCGCTCTCTCGAGCCAACTCATCCTCTTTCAGTTCTGGGGAAAGCTGCTCTTTCGAATCGTCACTCAGCTCTCACTGCA
CAAATGCAGGTGTCTCCGTCTTGGAAGTGCCCAGAGAAAACCAGCCTATTCACAGGGAGAAAGTGAAGCGCTACATCATAGAACACATTG
ACCTTGGGGCCTATTATTACCGCAAATTCTTCTATGGGAAAGAGCACCAAAACTACTTTGGAATAGATGAAAACCTTGGTCCAGTAGCAG
TCAGCATCCGGAGAGAGAAGGTGGAAGATGCCAAGGAGAAAGAAGGATCCCAGTTCAACTACAGGGTGGCTTTCAGGACAAGTGAGGTCA
CCAAGGAAAACAGAAACCACCTTCTGCCAGATATCGTGACGTGCGTGCAGAGCAGCAGGAAGTGAAGACACGTGCATTCCTGCCTTCCGT
GAAGGAGTGCCCAGTTCAAGAGGAGCCTGATGGAGCCCTGCCTGTCGAGGCTGTATGCCTATGGGGTTATGGAACCTTGTGGGCTTTTCT
AGAGAAAACTCAACAGCTGTTTCCCATAAAATGTTTAAAAGATCAAATTAGCCTTAATGCTGGATTGTCTGTACAAGATTAACTATCCAT
TGTGGCTTATCTATGCTTAAAGATTTCTTGTTTATTTCCTCTTGCAGTCATGCACATGATTTGGGTAAACTGTGAGATGAGAAATGGTTT
TCAGAGTATTAGATGGAATTCACCCCCGTTGAAGTTTATAAATGTGTTCAGGGGAAGCGGGAGGAAAGAGTTCACTGCCTAATCAGTTTT
GCATGTCATGAAAATTAAATTCCTCTCCAGGTGCAGCTTCAGCCTCATGCAACTTAAAGTGATAACAGTTATTTGATTTTTTAAAAAATA
TTATTCCAAAAGAAAACCATTTTAGGTCATCTCCCCCAACTCTGTTTGCTTACTGCTTAATAAATATAAAAATAAATCTGATGGTTACAG
ACAGGAGGCATTGTGTGGGAGGAATACACAACCTTTGGAAGTGTTGATAGCATCTGATATTCAGCCGACCAGATGACAAGAGCTCAGGCC
CACGGGTTTGCATAAGAGCACTGCTTTGCCTTAGTTTACTCGGGAGCAATTTTGAATCTTTCTATGCCTAGTTTCCCTTCCAGAAAAGCA
GGAAGTGGCTGTCATCTCAGGAGTGATGTCACACCACAGAAGGAAACTGTCAACCACTCCACACAACTGTGGAGAGTGCCCAGTGCCAGG
GGCTGGGCTTATCAGGAATAATGGTGTAGCAATGCGGAGTTCAGCCCATAACAGGGGTACTATAAAAATGAAGTAGGAAAGTAGAAGAGA
CCCCTGAAACCCCAGAACTGATAGAGGATAAAAACTTCCCTCCAAGTGGTAGATGGTACTGGAGTGATAAACAGTTCAGTGTTTTTAGGT
CATTTTTGGTGAAGATCTATGAATTTCCAGGATTTTTTTTTAACAAATTAGCATTGGCTACAAACCCACTGGTATAAGCAGCAGTGTGCC
TTCTCTCTAACTGTGGACAAGTCGGGCATGTGGCGGGTGAGGAGCCCTGGGCTGGGCACTGGGGCACAGTGAATGGGGCGGGAGGGGCTC
ACATCAAAACCAAAATGGCACGCAGCCCAGGTCTGGTTCCTCCATCAGTGTCTCTTTCCTCAGCGCTTTTCTTCCGAGGTAACTTTGTGA
AGCTTGACTTGGACTTGCCTAGCCTTGGAGGGACCACAACAGGGAGGCCTAATAGATTATGAACTAAGCCCTCAAAAGGGCTACCTGCCC
AGGAGGAGGAAGTGGGCATCTCCTTCCACAGTCCCTGCCTGGCGGGGCTGTTCAGGGAGACTGAGTTCCGAGCTCAGGATGTCTGGCAGG
CTGGCTGTGACTTCCAGCCACCATCACCAGGACACCGGTGTGGGCTGCATGCCTCAGTGGGCCAGGAGAGGCACGGCCTCTGAGTTGGGT
AGAGGCTTCCCACAAAGGCCTGGGAACCTGATCCTGGCCGTAAATCTGAAAGTACCACAGCCCTCAGGAGAACCAAGAGATAGGGAGGCA
GGCTGGGGAAATGTCATCAATGTGCACCCAGGCGTGGTGGAGCTGGTCAGCCCCAGCTGGAGTGGGACCCCATCAAGATGGAGCCTTTCC
TGGCACCTCCGGGAGGCCGTTTTGCGTTTCCGCCCTTCATGCATCTGAAACACCAAGGGCCATGTTCCTTCTGGTGCTTGTCCTTTTGAG
CTTGGTGTTTCAGCCGTGTCTGTTTTGTAGACTTTGATTTTGTCTTAAATGAGAAAGAAAGCTGGTGAAGGTTATTTCAAAGTTAAATAG
CTAGTCTGAGGGGCTTATCACTGAAGCCAGTTGTGCTTATGTGGGGTGGGAGTGTCACTGCCTACTTGAAAGTATGCACTTGTGTGGAAC
AGATTCAGGGTGGCCCCTAGCACTTGGGGCTGCGGGAGCTTCTGCACACTTTCCCTTTAACGGTAAAGAGACAAGCTTGGAGTGTTTAAG
TGGTTCGTTCAGGAGCACAGTGATAGCGGTGACAAAGGAGATTTGAACCCACGTCTGCGTGGCTCCAAAGTTCACTCTTTCATCACTCCC
TGCTGCGTCCTTCTTGAGGCTTTAGCATTTTTAGTGTGTTTTGTGCCCCCAGACCTCAGAGTTGACATTTAGCAGTGATAAACTGCTGTA
AATCCAAAGAACGTTTAGTGTCTCTTGTGGTGAGGTCCTGAAATGATTGTTGTATTAGTCAAACAGAATGATCATGGAGCATGTATGGAG
ATGTCAGATGCAATCCCTGTATTGTAAGGCAATGACATTTAATGAAGGATAAGATGAATTCACAGATAACTAGAACTCAGGGCCAAACGC
ACACAGCCTGTAGCAACAGTGTCATGCTGAGATTTAAAGGAAGAAGAGGTGCCGTGGCAGAACTCCACGTGACCGTCCCCTCCCTGCACG
CAGCCAGGATGAGAGGAGCAGAGCTGAGCGCCACCTCCCTGTCGGTGCCACGGCTGAGGTGAGGAGCTCTTGCCGGATGGTGGGGTGGGG
GCAGCAGGGCAGATTGAAGTCAGGGATTCTCTTATACCTGAGTTTGGAATGCCTCCTATTCAAACAAAGCAAAATATCTAACAGATGGTT
GGATATGAGTCTCAGGGAGGAATTCAATTTGAAAAGCACAGAATTAACATGTATTGCTTATATGAAGAATCTCAGCTAGAATAACAAGGT
CGGATGGGAGGAATCAGGACTGATTTGAAGCACGATTTACTAAATCATTCTTTCCTTTTCCTCCTTAGCAGATCATACCGCCAGCTGCTT
AACACGTAATAGTTTAATAAATTGTTTCTTCTTACCTCTCAGTGAGGGTAAGCACATGCAGGGAGATGGGTGAGTCTTTTAAATGGATAG
TGTCATCTCTGATGATCAGCCTTGACAGGGAGAGATCCTAGTAAAGCTGCAAATTCAGGCACTCAGTTCCCAGCCCTCCAGTTATCAAGG
GGGTGGGAACGCTGGTGGGCTGGAAAATGTGGAACAGACCTGCTCCTCTTCTTTTCCTGCCAATTACCGTATTCATAGAAGGTTGTGTCT
GTGGATCACACCTGTGTGTGTGCTGATGGCGGATGCTTGTGTAGCATAGTGACTTGGGACAAAACAGCATGGTAGATGAGGCTGGAGACG
GGTGGGCTAAGTAAACAGGCATTGCATTGCACATTTTGTGGGCAAAGAAGTTGAAGCATCGCATGATTTTAACAAATTACTTGCCAGATG
ATTTCAACACACTGCAAAATTTAGAATCAATAATGCCAAATTGGCCACATGATTTATATAAAACCAAGTGCTATGGTTTTAATATTATCT
TTAGAGGAGAAACCATTTTGATCTGTGTCCAAATAACTCTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTCGCTTGAGCTG
GAGTGCAGTGGTGCTATCTCGGCTCACTGTAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAACCTCCTGAGTAGCTGGGATT
ACAGGCACCCGCCACCACGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAAGCTGGTCTCGAACTCCT
GACCTCATGATTTGCCTGCCTCAGCCTACAAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCCCCCAAATAACTCTTGAACTG
GAAAATAACTCTTTAGCTATATACTGGCAGAATATTTGAACAACTCTAGCAAGAAATGTCAGTTTAGGGATGCCTCCTCTAAATGGGGGC
TTAGAATATAACATTTTGCAGGAAGTCCTTTCTGATACATAGCTGACTAGATGAAGGACCAGATTAACAAGTTCATGAGTTGTAAATATA
AAAGTTGTGTACCACGATAAAAAAGAAAAAGAAGTATGGCTGCACTGTTGATGGCTGGTCAAACAGCCCCCAAGAATCCTGGGGTGACTC
CAATACTGCCACCTTTTCTCTGTGGGTGCAGTTGCCTGCGGATGTGTGTGCACATCTGTGCCTCGGTATGCACACTCGAGATGCCCGCTC
TCATAGACGGTGCAGAGCGTCACTGCATTCCTATCTGATTAATGTGACCTTAGTGTTGTAGATACACTGTGTCACTTTCATCCTCCCTCC
TCCCCACAAAAGATGCCACGAGAACTCGTGAACTGTGATAAGCAATGAACAGAATAACTGTTGAAGAAGCACCTCATGAACCTCCCCAGA
GAAACGGGATGGAGGAGCACCCAGGGTGCTCTTGCTCTCTTGCCTGCGCTGCCATTTCCTTCCAGCCTGGGTTTCTAGCTCTTTGGGGAG
ATTCCCCGTTTTGTGGAATGCTTTCTGTGTTTCCTACTTCTGGATGCCTAAGGAGTGGCCAGTCATACTCCTGGCTGACCACTGCCAGGC
ACCGTGGTTTTCCTCACTGAACTCAAGGAGTCACCCTCCGTGGGGAGGCCACACTCACAGCTCCAGGCCTGCCATTTAGCCCTTGGGGCT
TGGCTGTAAAGTTGCCCAAGAGGATTACAGGAGCTGCCAGCCAAGTTTAATTTGGCCACCTTAGAGAACTGCAGCAAGGCCCTATCAGCT
TCCCATTAGACAAACAACTGCATTTAAATTAAATAAAGTTTGCACCTCTAGGGAGTGCTGACCTGAAAATAAGAACCTTCTGTCTGTGAT
TATAGAGTACACTTGCTTTTATTAATTGCTGATTCTTAGTTTACAAAAAAAAAAATTAGAAAAGCATTACCATTTACTTTCCAAGGGGCA
AGAGATTCTCTACAATACCCTTCCCCCAACCCTCTCCTCAAATTTCCAAATCCTAAATACTTTGAAGAAATTTGTGTGACTGTTTAAAAT
TGAGTATTTCCTTCTAACTATTGTCTTTTGAAAAGGGATGGTTCACCAGGCCAGTGATACTCTATGGACTGCATTTTGGGACCTCTACCC
CAGCAAGGATACAGGTTCCTGGGGTCTTGAAGATGGGAAAAGTTGTCTCAGAATTTACCCAAATGTCGTTCTCACCATAAAAGATATACT
TGTAGAAATGAGAAGCTTCAGTATAACTCAAAACACTGGACGCAGCAATAACTATAAACATTTTAATTTCAAAAACAAAGGTGTGTGCGA
TGTTGTGTGCACAGTAAGGGTTGCGGGGCTTGGAGAACAAGCACGCGTCCCTGTGAAGCCCGCAGGGTGCTGGCGGCCCACCAATCGCCT
GGACTACAGTGAGGAGCATTGTGTGACTCCGCGGTGGATTTCCATGCACCGAATGGACTCAGTTTCTAAACTCACATCCTAACGTATCCT
GGCTTTTCACAGAATACTGGAGACATGACTGCATGCATGATCACGGTTCTTGTTGTGAAGCTGCCACCATGTTACGCTTAACAGCTGCAT
AAATATTATAAAGAAATAGGGTTTTCTTGACACTTAGATTTAACCTTAATGCATCTGCCCAGCTGATGGTATCAGACGTGCTGCTGTTCA

>81948_81948_1_SIPA1L2-NTPCR_SIPA1L2_chr1_232629273_ENST00000366630_NTPCR_chr1_233113909_ENST00000366628_length(amino acids)=572AA_BP=550
MVRLGGSSSVDMSDPRQSQEEKHKLGRASSKFKDPPRIMQSDDYFARKFKAINGNMGPTTSLNASNSNETGGGGPANGTPAVPKMGVRAR
VSEWPPKKDCSKELTCKALWESRSQTSYESITSVLQNGQSDQSEGQQDEQLDLDFVEAKYTIGDIFVHSPQRGLHPIRQRSNSDVTISDI
DAEDVLDQNAVNPNTGAALHREYGSTSSIDRQGLSGENFFAMLRGYRVENYDHKAMVPFGFPEFFRCDPAISPSLHAAAQISRGEFVRIS
GLDYVDSALLMGRDRDKPFKRRLKSESVETSLFRKLRTVKSEHETFKFTSELEESRLERGIRPWNCQRCFAHYDVQSILFNINEAMATRA
NVGKRKNITTGASAASQTQMPTGQTGNCESPLGSKEDLNSKENLDADEGDGKSNDLVLSCPYFRNETGGEGDRRIALSRANSSSFSSGES
CSFESSLSSHCTNAGVSVLEVPRENQPIHREKVKRYIIEHIDLGAYYYRKFFYGKEHQNYFGIDENLGPVAVSIRREKVEDAKEKEGSQF

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Fusion Gene PPI Analysis for SIPA1L2-NTPCR


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 SIPA1L2-NTPCR


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 SIPA1L2-NTPCR


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource