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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:UBAP2L-CREB3L1 (FusionGDB2 ID:95279)

Fusion Gene Summary for UBAP2L-CREB3L1

check button Fusion gene summary
Fusion gene informationFusion gene name: UBAP2L-CREB3L1
Fusion gene ID: 95279
HgeneTgene
Gene symbol

UBAP2L

CREB3L1

Gene ID

9898

90993

Gene nameubiquitin associated protein 2 likecAMP responsive element binding protein 3 like 1
SynonymsNICE-4|NICE4OASIS|OI16
Cytomap

1q21.3

11p11.2

Type of geneprotein-codingprotein-coding
Descriptionubiquitin-associated protein 2-likeprotein NICE-4cyclic AMP-responsive element-binding protein 3-like protein 1BBF-2 homologcAMP-responsive element-binding protein 3-like protein 1old astrocyte specifically-induced substance
Modification date2020031320200327
UniProtAcc.

Q96BA8

Ensembl transtripts involved in fusion geneENST00000343815, ENST00000428931, 
ENST00000271877, ENST00000361546, 
ENST00000484819, 
ENST00000529193, 
ENST00000288400, ENST00000534616, 
Fusion gene scores* DoF score8 X 8 X 5=32010 X 10 X 4=400
# samples 98
** MAII scorelog2(9/320*10)=-1.83007499855769
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/400*10)=-2.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: UBAP2L [Title/Abstract] AND CREB3L1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointUBAP2L(154234173)-CREB3L1(46321486), # samples:1
Anticipated loss of major functional domain due to fusion event.UBAP2L-CREB3L1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
UBAP2L-CREB3L1 seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted ORF.
UBAP2L-CREB3L1 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
UBAP2L-CREB3L1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
UBAP2L-CREB3L1 seems lost the major protein functional domain in Tgene 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
TgeneCREB3L1

GO:0010629

negative regulation of gene expression

27121396

TgeneCREB3L1

GO:0032967

positive regulation of collagen biosynthetic process

25310401

TgeneCREB3L1

GO:0040037

negative regulation of fibroblast growth factor receptor signaling pathway

27121396

TgeneCREB3L1

GO:0045892

negative regulation of transcription, DNA-templated

27121396


check buttonFusion gene breakpoints across UBAP2L (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 CREB3L1 (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
ChimerDB4UCECTCGA-EY-A210-01AUBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+


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Fusion Gene ORF analysis for UBAP2L-CREB3L1

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-shiftENST00000343815ENST00000529193UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
Frame-shiftENST00000343815ENST00000288400UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
5CDS-intronENST00000343815ENST00000534616UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
Frame-shiftENST00000428931ENST00000529193UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
Frame-shiftENST00000428931ENST00000288400UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
5CDS-intronENST00000428931ENST00000534616UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
Frame-shiftENST00000271877ENST00000529193UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
Frame-shiftENST00000271877ENST00000288400UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
5CDS-intronENST00000271877ENST00000534616UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
Frame-shiftENST00000361546ENST00000529193UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
Frame-shiftENST00000361546ENST00000288400UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
5CDS-intronENST00000361546ENST00000534616UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
intron-3CDSENST00000484819ENST00000529193UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
intron-3CDSENST00000484819ENST00000288400UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+
intron-intronENST00000484819ENST00000534616UBAP2Lchr1

154234173

+CREB3L1chr11

46321486

+

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 UBAP2L-CREB3L1


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)
UBAP2Lchr1154234173+CREB3L1chr1146321485+2.66E-101
UBAP2Lchr1154234173+CREB3L1chr1146321485+2.66E-101

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 UBAP2L-CREB3L1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.CREB3L1

Q96BA8

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Transcription factor involved in unfolded protein response (UPR). Binds the DNA consensus sequence 5'-GTGXGCXGC-3' (PubMed:21767813). In the absence of endoplasmic reticulum (ER) stress, inserted into ER membranes, with N-terminal DNA-binding and transcription activation domains oriented toward the cytosolic face of the membrane. In response to ER stress, transported to the Golgi, where it is cleaved in a site-specific manner by resident proteases S1P/MBTPS1 and S2P/MBTPS2. The released N-terminal cytosolic domain is translocated to the nucleus to effect transcription of specific target genes. Plays a critical role in bone formation through the transcription of COL1A1, and possibly COL1A2, and the secretion of bone matrix proteins. Directly binds to the UPR element (UPRE)-like sequence in an osteoblast-specific COL1A1 promoter region and induces its transcription. Does not regulate COL1A1 in other tissues, such as skin (By similarity). Required to protect astrocytes from ER stress-induced cell death. In astrocytes, binds to the cAMP response element (CRE) of the BiP/HSPA5 promoter and participate in its transcriptional activation (By similarity). Required for TGFB1 to activate genes involved in the assembly of collagen extracellular matrix (PubMed:25310401). {ECO:0000250|UniProtKB:Q9Z125, ECO:0000269|PubMed:12054625, ECO:0000269|PubMed:21767813, ECO:0000269|PubMed:25310401}.; FUNCTION: (Microbial infection) May play a role in limiting virus spread by inhibiting proliferation of virus-infected cells. Upon infection with diverse DNA and RNA viruses, inhibits cell-cycle progression by binding to promoters and activating transcription of genes encoding cell-cycle inhibitors, such as p21/CDKN1A (PubMed:21767813). {ECO:0000269|PubMed:21767813}.

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 UBAP2L-CREB3L1


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 UBAP2L-CREB3L1


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 UBAP2L-CREB3L1


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 UBAP2L-CREB3L1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneCREB3L1C0268362Osteogenesis imperfecta type III (disorder)1ORPHANET
TgeneCREB3L1C4015610OSTEOGENESIS IMPERFECTA, TYPE XVI1GENOMICS_ENGLAND