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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-SNX5 (FusionGDB2 ID:HG51084TG27131)

Fusion Gene Summary for CRYL1-SNX5

check button Fusion gene summary
Fusion gene informationFusion gene name: CRYL1-SNX5
Fusion gene ID: hg51084tg27131
HgeneTgene
Gene symbol

CRYL1

SNX5

Gene ID

51084

27131

Gene namecrystallin lambda 1sorting nexin 5
SynonymsGDH|HEL30|gul3DH|lambda-CRY-
Cytomap('CRYL1')('SNX5')

13q12.11

20p11.23

Type of geneprotein-codingprotein-coding
Descriptionlambda-crystallin homologL-gulonate 3-dehydrogenasecrystallin, lamda 1epididymis luminal protein 30testicular tissue protein Li 44sorting nexin-5
Modification date2020031320200320
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000298248, ENST00000382812, 
ENST00000480748, 
Fusion gene scores* DoF score13 X 11 X 6=85815 X 9 X 6=810
# samples 1317
** MAII scorelog2(13/858*10)=-2.72246602447109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(17/810*10)=-2.25238716163429
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CRYL1 [Title/Abstract] AND SNX5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCRYL1(21006240)-SNX5(17923839), # 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
TgeneSNX5

GO:0006907

pinocytosis

18854019



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
ChimerDB4PRADTCGA-HC-8260CRYL1chr13

21006240

-SNX5chr20

17923839

-


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Fusion Gene ORF analysis for CRYL1-SNX5

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-5UTRENST00000298248ENST00000377759CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-5UTRENST00000298248ENST00000377768CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-5UTRENST00000298248ENST00000483485CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-5UTRENST00000382812ENST00000377759CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-5UTRENST00000382812ENST00000377768CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-5UTRENST00000382812ENST00000483485CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-intronENST00000298248ENST00000481323CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-intronENST00000298248ENST00000486039CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-intronENST00000298248ENST00000606557CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-intronENST00000298248ENST00000606602CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-intronENST00000382812ENST00000481323CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-intronENST00000382812ENST00000486039CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-intronENST00000382812ENST00000606557CRYL1chr13

21006240

-SNX5chr20

17923839

-
5CDS-intronENST00000382812ENST00000606602CRYL1chr13

21006240

-SNX5chr20

17923839

-
5UTR-5UTRENST00000480748ENST00000377759CRYL1chr13

21006240

-SNX5chr20

17923839

-
5UTR-5UTRENST00000480748ENST00000377768CRYL1chr13

21006240

-SNX5chr20

17923839

-
5UTR-5UTRENST00000480748ENST00000483485CRYL1chr13

21006240

-SNX5chr20

17923839

-
5UTR-intronENST00000480748ENST00000481323CRYL1chr13

21006240

-SNX5chr20

17923839

-
5UTR-intronENST00000480748ENST00000486039CRYL1chr13

21006240

-SNX5chr20

17923839

-
5UTR-intronENST00000480748ENST00000606557CRYL1chr13

21006240

-SNX5chr20

17923839

-
5UTR-intronENST00000480748ENST00000606602CRYL1chr13

21006240

-SNX5chr20

17923839

-

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-SNX5


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 CRYL1-SNX5


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/:21006240/:17923839)
- 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 CRYL1-SNX5


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-SNX5


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-SNX5


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-SNX5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCRYL1C0033578Prostatic Neoplasms1CTD_human
HgeneCRYL1C0376358Malignant neoplasm of prostate1CTD_human
HgeneCRYL1C0520459Necrotizing Enterocolitis1CTD_human
TgeneC0024623Malignant neoplasm of stomach1CTD_human
TgeneC0038356Stomach Neoplasms1CTD_human
TgeneC0235874Disease Exacerbation1CTD_human
TgeneC1708349Hereditary Diffuse Gastric Cancer1CTD_human