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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:CRYL1-PDCD10 (FusionGDB2 ID:19613)

Fusion Gene Summary for CRYL1-PDCD10

check button Fusion gene summary
Fusion gene informationFusion gene name: CRYL1-PDCD10
Fusion gene ID: 19613
HgeneTgene
Gene symbol

CRYL1

PDCD10

Gene ID

51084

11235

Gene namecrystallin lambda 1programmed cell death 10
SynonymsGDH|HEL30|gul3DH|lambda-CRYCCM3|TFAR15
Cytomap

13q12.11

3q26.1

Type of geneprotein-codingprotein-coding
Descriptionlambda-crystallin homologL-gulonate 3-dehydrogenasecrystallin, lamda 1epididymis luminal protein 30testicular tissue protein Li 44programmed cell death protein 10TF-1 cell apoptosis-related protein 15apoptosis-related protein 15cerebral cavernous malformations 3 protein
Modification date2020031320200313
UniProtAcc

Q9Y2S2

.
Ensembl transtripts involved in fusion geneENST00000298248, ENST00000382812, 
ENST00000480748, 
ENST00000392750, 
ENST00000473645, ENST00000497056, 
ENST00000461494, ENST00000470131, 
ENST00000471885, ENST00000487947, 
ENST00000492396, ENST00000487678, 
Fusion gene scores* DoF score13 X 11 X 6=8584 X 4 X 3=48
# samples 134
** MAII scorelog2(13/858*10)=-2.72246602447109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CRYL1 [Title/Abstract] AND PDCD10 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCRYL1(20978018)-PDCD10(167414914), # 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
TgenePDCD10

GO:0008284

positive regulation of cell proliferation

17360971|23541896

TgenePDCD10

GO:0030335

positive regulation of cell migration

23541896

TgenePDCD10

GO:0032874

positive regulation of stress-activated MAPK cascade

22652780

TgenePDCD10

GO:0042542

response to hydrogen peroxide

22291017

TgenePDCD10

GO:0043066

negative regulation of apoptotic process

17360971

TgenePDCD10

GO:0043406

positive regulation of MAP kinase activity

17360971


check buttonFusion gene breakpoints across CRYL1 (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 PDCD10 (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/AFN148303CRYL1chr13

20978018

+PDCD10chr3

167414914

-


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Fusion Gene ORF analysis for CRYL1-PDCD10

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
intron-3CDSENST00000298248ENST00000392750CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-3CDSENST00000298248ENST00000473645CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-3CDSENST00000298248ENST00000497056CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-3CDSENST00000382812ENST00000392750CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-3CDSENST00000382812ENST00000473645CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-3CDSENST00000382812ENST00000497056CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-3CDSENST00000480748ENST00000392750CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-3CDSENST00000480748ENST00000473645CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-3CDSENST00000480748ENST00000497056CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000298248ENST00000461494CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000298248ENST00000470131CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000298248ENST00000471885CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000298248ENST00000487947CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000298248ENST00000492396CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000382812ENST00000461494CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000382812ENST00000470131CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000382812ENST00000471885CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000382812ENST00000487947CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000382812ENST00000492396CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000480748ENST00000461494CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000480748ENST00000470131CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000480748ENST00000471885CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000480748ENST00000487947CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-5UTRENST00000480748ENST00000492396CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-intronENST00000298248ENST00000487678CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-intronENST00000382812ENST00000487678CRYL1chr13

20978018

+PDCD10chr3

167414914

-
intron-intronENST00000480748ENST00000487678CRYL1chr13

20978018

+PDCD10chr3

167414914

-

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 CRYL1-PDCD10


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)

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 CRYL1-PDCD10


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/:20978018/:167414914)
- 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
CRYL1

Q9Y2S2

.
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 CRYL1-PDCD10


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 CRYL1-PDCD10


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 CRYL1-PDCD10


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 CRYL1-PDCD10


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