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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:RAMP1-PASK (FusionGDB2 ID:HG10267TG23178)

Fusion Gene Summary for RAMP1-PASK

check button Fusion gene summary
Fusion gene informationFusion gene name: RAMP1-PASK
Fusion gene ID: hg10267tg23178
HgeneTgene
Gene symbol

RAMP1

PASK

Gene ID

10267

23178

Gene namereceptor activity modifying protein 1PAS domain containing serine/threonine kinase
Synonyms-PASKIN|STK37
Cytomap('RAMP1')('PASK')

2q37.3

2q37.3

Type of geneprotein-codingprotein-coding
Descriptionreceptor activity-modifying protein 1CRLR activity-modifying protein 1calcitonin receptor-like receptor activity modifying protein 1receptor (G protein-coupled) activity modifying protein 1receptor (calcitonin) activity modifying protein 1PAS domain-containing serine/threonine-protein kinaseper-arnt-sim (PAS) domain kinase
Modification date2020031320200329
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000254661, ENST00000403885, 
ENST00000404910, ENST00000409726, 
Fusion gene scores* DoF score10 X 8 X 6=4803 X 3 X 3=27
# samples 83
** MAII scorelog2(8/480*10)=-2.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: RAMP1 [Title/Abstract] AND PASK [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointRAMP1(238786003)-PASK(242077981), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneRAMP1

GO:0001525

angiogenesis

20596610

HgeneRAMP1

GO:0006816

calcium ion transport

10882736

HgeneRAMP1

GO:0007189

adenylate cyclase-activating G protein-coupled receptor signaling pathway

14722252

HgeneRAMP1

GO:0015031

protein transport

10882736

HgeneRAMP1

GO:0031623

receptor internalization

10882736|15613468

HgeneRAMP1

GO:0060050

positive regulation of protein glycosylation

9620797

HgeneRAMP1

GO:0072659

protein localization to plasma membrane

10882736

HgeneRAMP1

GO:0097647

amylin receptor signaling pathway

14722252

TgenePASK

GO:0006468

protein phosphorylation

16275910

TgenePASK

GO:0045719

negative regulation of glycogen biosynthetic process

16275910

TgenePASK

GO:0046777

protein autophosphorylation

20943661|21418524



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
ChimerDB4THYMTCGA-XH-A853-01ARAMP1chr2

238786003

+PASKchr2

242077981

+


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Fusion Gene ORF analysis for RAMP1-PASK

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-intronENST00000254661ENST00000234040RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000254661ENST00000358649RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000254661ENST00000403638RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000254661ENST00000405260RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000254661ENST00000475666RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000254661ENST00000539818RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000254661ENST00000544142RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000403885ENST00000234040RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000403885ENST00000358649RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000403885ENST00000403638RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000403885ENST00000405260RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000403885ENST00000475666RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000403885ENST00000539818RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000403885ENST00000544142RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000404910ENST00000234040RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000404910ENST00000358649RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000404910ENST00000403638RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000404910ENST00000405260RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000404910ENST00000475666RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000404910ENST00000539818RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000404910ENST00000544142RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000409726ENST00000234040RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000409726ENST00000358649RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000409726ENST00000403638RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000409726ENST00000405260RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000409726ENST00000475666RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000409726ENST00000539818RAMP1chr2

238786003

+PASKchr2

242077981

+
5CDS-intronENST00000409726ENST00000544142RAMP1chr2

238786003

+PASKchr2

242077981

+

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 RAMP1-PASK


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)


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Fusion Protein Features for RAMP1-PASK


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/:238786003/:242077981)
- 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

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for RAMP1-PASK


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 RAMP1-PASK


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 RAMP1-PASK


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 RAMP1-PASK


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRAMP1C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneC0004352Autistic Disorder1CTD_human
TgeneC2931817Chromosome 2q37 deletion syndrome1CTD_human