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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:C1RL-PRODH (FusionGDB2 ID:HG51279TG5625)

Fusion Gene Summary for C1RL-PRODH

check button Fusion gene summary
Fusion gene informationFusion gene name: C1RL-PRODH
Fusion gene ID: hg51279tg5625
HgeneTgene
Gene symbol

C1RL

PRODH

Gene ID

51279

5625

Gene namecomplement C1r subcomponent likeproline dehydrogenase 1
SynonymsC1RL1|C1RLP|C1r-LP|CLSPaHSPOX2|PIG6|POX|PRODH1|PRODH2|TP53I6
Cytomap('C1RL')('PRODH')

12p13.31

22q11.21

Type of geneprotein-codingprotein-coding
Descriptioncomplement C1r subcomponent-like proteinC1r-like proteinC1r-like serine protease analog proteincomplement C1r-like proteinasecomplement component 1, r subcomponent-likeproline dehydrogenase 1, mitochondrialp53-induced gene 6 proteinproline dehydrogenase (oxidase) 1proline oxidase 2proline oxidase, mitochondrialtumor protein p53 inducible protein 6
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000266542, ENST00000544702, 
ENST00000504702, ENST00000545280, 
ENST00000545337, 
Fusion gene scores* DoF score5 X 5 X 3=756 X 4 X 6=144
# samples 56
** MAII scorelog2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/144*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: C1RL [Title/Abstract] AND PRODH [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointC1RL(7254494)-PRODH(18913235), # samples:1
Anticipated loss of major functional domain due to fusion event.C1RL-PRODH seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
C1RL-PRODH seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
C1RL-PRODH 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
TgenePRODH

GO:0010942

positive regulation of cell death

23743200



check button Fusion gene information
* 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
ChimerDB4KIRCTCGA-A3-3370-01AC1RLchr12

7254494

-PRODHchr22

18913235

-


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Fusion Gene ORF analysis for C1RL-PRODH

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-shiftENST00000266542ENST00000334029C1RLchr12

7254494

-PRODHchr22

18913235

-
Frame-shiftENST00000266542ENST00000357068C1RLchr12

7254494

-PRODHchr22

18913235

-
Frame-shiftENST00000266542ENST00000420436C1RLchr12

7254494

-PRODHchr22

18913235

-
Frame-shiftENST00000544702ENST00000334029C1RLchr12

7254494

-PRODHchr22

18913235

-
Frame-shiftENST00000544702ENST00000357068C1RLchr12

7254494

-PRODHchr22

18913235

-
Frame-shiftENST00000544702ENST00000420436C1RLchr12

7254494

-PRODHchr22

18913235

-
intron-3CDSENST00000504702ENST00000334029C1RLchr12

7254494

-PRODHchr22

18913235

-
intron-3CDSENST00000504702ENST00000357068C1RLchr12

7254494

-PRODHchr22

18913235

-
intron-3CDSENST00000504702ENST00000420436C1RLchr12

7254494

-PRODHchr22

18913235

-
intron-3CDSENST00000545280ENST00000334029C1RLchr12

7254494

-PRODHchr22

18913235

-
intron-3CDSENST00000545280ENST00000357068C1RLchr12

7254494

-PRODHchr22

18913235

-
intron-3CDSENST00000545280ENST00000420436C1RLchr12

7254494

-PRODHchr22

18913235

-
intron-3CDSENST00000545337ENST00000334029C1RLchr12

7254494

-PRODHchr22

18913235

-
intron-3CDSENST00000545337ENST00000357068C1RLchr12

7254494

-PRODHchr22

18913235

-
intron-3CDSENST00000545337ENST00000420436C1RLchr12

7254494

-PRODHchr22

18913235

-

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 C1RL-PRODH


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 C1RL-PRODH


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/:7254494/:18913235)
- 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 C1RL-PRODH


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 C1RL-PRODH


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 C1RL-PRODH


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 C1RL-PRODH


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC0268529Proline dehydrogenase deficiency7CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneC1833247SCHIZOPHRENIA 4 (disorder)3GENOMICS_ENGLAND;UNIPROT
TgeneC0005586Bipolar Disorder2PSYGENET
TgeneC0002514Amino Acid Metabolism, Inborn Errors1CTD_human
TgeneC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneC0027765nervous system disorder1CTD_human
TgeneC0036341Schizophrenia1CTD_human
TgeneC0750905Amino Acid Metabolism, Inherited Disorders1CTD_human