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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:CREB3L2-GREM1 (FusionGDB2 ID:HG64764TG26585)

Fusion Gene Summary for CREB3L2-GREM1

check button Fusion gene summary
Fusion gene informationFusion gene name: CREB3L2-GREM1
Fusion gene ID: hg64764tg26585
HgeneTgene
Gene symbol

CREB3L2

GREM1

Gene ID

64764

26585

Gene namecAMP responsive element binding protein 3 like 2gremlin 1, DAN family BMP antagonist
SynonymsBBF2H7C15DUPq|CKTSF1B1|CRAC1|CRCS4|DAND2|DRM|DUP15q|GREMLIN|HMPS|HMPS1|IHG-2|MPSH|PIG2
Cytomap('CREB3L2')('GREM1')

7q33

15q13.3

Type of geneprotein-codingprotein-coding
Descriptioncyclic AMP-responsive element-binding protein 3-like protein 2B-ZIB transcription factorBBF2 human homolog on chromosome 7FUS/BBF2H7 proteinTCAG_1951439basic transcription factor 2cAMP-responsive element-binding protein 3-like protein 2gremlin-1DAN domain family member 2cell proliferation-inducing gene 2 proteincolorectal adenoma and carcinoma 1cysteine knot superfamily 1, BMP antagonist 1down-regulated in Mos-transformed cells proteingremlin 1, cysteine knot superfamily, homolog
Modification date2020031320200313
UniProtAcc

Q70SY1

.
Ensembl transtripts involved in fusion geneENST00000330387, ENST00000452463, 
ENST00000456390, ENST00000468127, 
ENST00000458726, 
Fusion gene scores* DoF score15 X 16 X 7=16801 X 1 X 1=1
# samples 181
** MAII scorelog2(18/1680*10)=-3.22239242133645
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: CREB3L2 [Title/Abstract] AND GREM1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCREB3L2(137686350)-GREM1(33022891), # 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
HgeneCREB3L2

GO:0045893

positive regulation of transcription, DNA-templated

17178827

TgeneGREM1

GO:0000902

cell morphogenesis

16545136

TgeneGREM1

GO:0008284

positive regulation of cell proliferation

16545136

TgeneGREM1

GO:0030514

negative regulation of BMP signaling pathway

15539560

TgeneGREM1

GO:0051973

positive regulation of telomerase activity

16545136

TgeneGREM1

GO:0060394

negative regulation of pathway-restricted SMAD protein phosphorylation

15539560

TgeneGREM1

GO:0090090

negative regulation of canonical Wnt signaling pathway

15539560



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
ChimerDB4STADTCGA-BR-8077-01ACREB3L2chr7

137686350

-GREM1chr15

33022891

+


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Fusion Gene ORF analysis for CREB3L2-GREM1

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-5UTRENST00000330387ENST00000300177CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000330387ENST00000322805CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000330387ENST00000560677CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000330387ENST00000560830CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000452463ENST00000300177CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000452463ENST00000322805CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000452463ENST00000560677CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000452463ENST00000560830CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000456390ENST00000300177CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000456390ENST00000322805CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000456390ENST00000560677CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5CDS-5UTRENST00000456390ENST00000560830CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5UTR-5UTRENST00000468127ENST00000300177CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5UTR-5UTRENST00000468127ENST00000322805CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5UTR-5UTRENST00000468127ENST00000560677CREB3L2chr7

137686350

-GREM1chr15

33022891

+
5UTR-5UTRENST00000468127ENST00000560830CREB3L2chr7

137686350

-GREM1chr15

33022891

+
intron-5UTRENST00000458726ENST00000300177CREB3L2chr7

137686350

-GREM1chr15

33022891

+
intron-5UTRENST00000458726ENST00000322805CREB3L2chr7

137686350

-GREM1chr15

33022891

+
intron-5UTRENST00000458726ENST00000560677CREB3L2chr7

137686350

-GREM1chr15

33022891

+
intron-5UTRENST00000458726ENST00000560830CREB3L2chr7

137686350

-GREM1chr15

33022891

+

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 CREB3L2-GREM1


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)
CREB3L2chr7137686349-GREM1chr1533022891+2.21E-050.9999778
CREB3L2chr7137686349-GREM1chr1533022891+2.21E-050.9999778


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.
genomic feature of top 1%

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Fusion Protein Features for CREB3L2-GREM1


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/:137686350/:33022891)
- 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
CREB3L2

Q70SY1

.
FUNCTION: Transcription factor involved in unfolded protein response (UPR). 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 chondrogenesis by activating the transcription of SEC23A, which promotes the transport and secretion of cartilage matrix proteins, and possibly that of ER biogenesis-related genes (By similarity). In a neuroblastoma cell line, protects cells from ER stress-induced death (PubMed:17178827). In vitro activates transcription of target genes via direct binding to the CRE site (PubMed:17178827). {ECO:0000250|UniProtKB:Q8BH52, ECO:0000269|PubMed:17178827}.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 CREB3L2-GREM1


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 CREB3L2-GREM1


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 CREB3L2-GREM1


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 CREB3L2-GREM1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC1832587POLYPOSIS SYNDROME, HEREDITARY MIXED, 18CLINGEN;GENOMICS_ENGLAND;ORPHANET
TgeneC0009402Colorectal Carcinoma2CTD_human
TgeneC0009404Colorectal Neoplasms2CTD_human
TgeneC0024623Malignant neoplasm of stomach1CTD_human
TgeneC0032580Adenomatous Polyposis Coli1CTD_human
TgeneC0034069Pulmonary Fibrosis1CTD_human
TgeneC0038356Stomach Neoplasms1CTD_human
TgeneC1708349Hereditary Diffuse Gastric Cancer1CTD_human
TgeneC2677290COLORECTAL CANCER, SUSCEPTIBILITY TO, 41ORPHANET
TgeneC2677291COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 151ORPHANET
TgeneC2713442Polyposis, Adenomatous Intestinal1CTD_human
TgeneC2713443Familial Intestinal Polyposis1CTD_human
TgeneC4721507Alveolitis, Fibrosing1CTD_human