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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:CTNNA1-EGR1 (FusionGDB2 ID:20254)

Fusion Gene Summary for CTNNA1-EGR1

check button Fusion gene summary
Fusion gene informationFusion gene name: CTNNA1-EGR1
Fusion gene ID: 20254
HgeneTgene
Gene symbol

CTNNA1

EGR1

Gene ID

1495

1958

Gene namecatenin alpha 1early growth response 1
SynonymsCAP102|MDPT2AT225|G0S30|KROX-24|NGFI-A|TIS8|ZIF-268|ZNF225
Cytomap

5q31.2

5q31.2

Type of geneprotein-codingprotein-coding
Descriptioncatenin alpha-1alpha-E-catenincatenin (cadherin-associated protein), alpha 1, 102kDaepididymis secretory sperm binding proteinrenal carcinoma antigen NY-REN-13early growth response protein 1EGR-1nerve growth factor-induced protein Atranscription factor ETR103transcription factor Zif268zinc finger protein 225zinc finger protein Krox-24
Modification date2020031320200313
UniProtAcc.

P18146

Ensembl transtripts involved in fusion geneENST00000355078, ENST00000302763, 
ENST00000518825, ENST00000520400, 
ENST00000540387, 
ENST00000239938, 
Fusion gene scores* DoF score25 X 19 X 12=57007 X 10 X 3=210
# samples 3411
** MAII scorelog2(34/5700*10)=-4.06735526780176
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/210*10)=-0.932885804141463
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CTNNA1 [Title/Abstract] AND EGR1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCTNNA1(138163407)-EGR1(137802446), # samples:2
CTNNA1(138163407)-EGR1(137802445), # samples:2
Anticipated loss of major functional domain due to fusion event.CTNNA1-EGR1 seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted ORF.
CTNNA1-EGR1 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
HgeneCTNNA1

GO:0071681

cellular response to indole-3-methanol

10868478

TgeneEGR1

GO:0006366

transcription by RNA polymerase II

19057511

TgeneEGR1

GO:0033233

regulation of protein sumoylation

19057511

TgeneEGR1

GO:0045893

positive regulation of transcription, DNA-templated

12560508

TgeneEGR1

GO:0045944

positive regulation of transcription by RNA polymerase II

19057511

TgeneEGR1

GO:0098759

cellular response to interleukin-8

20363028

TgeneEGR1

GO:1902895

positive regulation of pri-miRNA transcription by RNA polymerase II

19307576


check buttonFusion gene breakpoints across CTNNA1 (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 EGR1 (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
ChimerDB4ESCATCGA-L5-A4OQ-01ACTNNA1chr5

138163407

+EGR1chr5

137802446

+
ChimerDB4ESCATCGA-L5-A4OQCTNNA1chr5

138163407

+EGR1chr5

137802445

+
ChimerDB4ESCATCGA-L5-A4OQCTNNA1chr5

138163407

+EGR1chr5

137802445

+
ChimerDB4ESCATCGA-L5-A4OQ-01ACTNNA1chr5

138163407

-EGR1chr5

137802446

+


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Fusion Gene ORF analysis for CTNNA1-EGR1

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-shiftENST00000355078ENST00000239938CTNNA1chr5

138163407

+EGR1chr5

137802446

+
Frame-shiftENST00000302763ENST00000239938CTNNA1chr5

138163407

+EGR1chr5

137802446

+
Frame-shiftENST00000518825ENST00000239938CTNNA1chr5

138163407

+EGR1chr5

137802446

+
intron-3CDSENST00000520400ENST00000239938CTNNA1chr5

138163407

+EGR1chr5

137802446

+
intron-3CDSENST00000540387ENST00000239938CTNNA1chr5

138163407

+EGR1chr5

137802446

+
Frame-shiftENST00000355078ENST00000239938CTNNA1chr5

138163407

+EGR1chr5

137802445

+
Frame-shiftENST00000302763ENST00000239938CTNNA1chr5

138163407

+EGR1chr5

137802445

+
Frame-shiftENST00000518825ENST00000239938CTNNA1chr5

138163407

+EGR1chr5

137802445

+
intron-3CDSENST00000520400ENST00000239938CTNNA1chr5

138163407

+EGR1chr5

137802445

+
intron-3CDSENST00000540387ENST00000239938CTNNA1chr5

138163407

+EGR1chr5

137802445

+

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 CTNNA1-EGR1


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)
CTNNA1chr5138163407+EGR1chr5137802445+2.60E-050.999974
CTNNA1chr5138163407+EGR1chr5137802445+2.60E-050.999974
CTNNA1chr5138163407+EGR1chr5137802445+2.60E-050.999974
CTNNA1chr5138163407+EGR1chr5137802445+2.60E-050.999974

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 CTNNA1-EGR1


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
.EGR1

P18146

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: Transcriptional regulator (PubMed:20121949). Recognizes and binds to the DNA sequence 5'-GCG(T/G)GGGCG-3'(EGR-site) in the promoter region of target genes (By similarity). Binds double-stranded target DNA, irrespective of the cytosine methylation status (PubMed:25258363, PubMed:25999311). Regulates the transcription of numerous target genes, and thereby plays an important role in regulating the response to growth factors, DNA damage, and ischemia. Plays a role in the regulation of cell survival, proliferation and cell death. Activates expression of p53/TP53 and TGFB1, and thereby helps prevent tumor formation. Required for normal progress through mitosis and normal proliferation of hepatocytes after partial hepatectomy. Mediates responses to ischemia and hypoxia; regulates the expression of proteins such as IL1B and CXCL2 that are involved in inflammatory processes and development of tissue damage after ischemia. Regulates biosynthesis of luteinizing hormone (LHB) in the pituitary (By similarity). Regulates the amplitude of the expression rhythms of clock genes: ARNTL/BMAL1, PER2 and NR1D1 in the liver via the activation of PER1 (clock repressor) transcription. Regulates the rhythmic expression of core-clock gene ARNTL/BMAL1 in the suprachiasmatic nucleus (SCN) (By similarity). {ECO:0000250|UniProtKB:P08046, ECO:0000269|PubMed:20121949, ECO:0000269|PubMed:25258363, ECO:0000269|PubMed:25999311}.

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 CTNNA1-EGR1


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 CTNNA1-EGR1


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 CTNNA1-EGR1


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 CTNNA1-EGR1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCTNNA1C1708349Hereditary Diffuse Gastric Cancer3ORPHANET
HgeneCTNNA1C0023467Leukemia, Myelocytic, Acute1CTD_human
HgeneCTNNA1C0026998Acute Myeloid Leukemia, M11CTD_human
HgeneCTNNA1C0238198Gastrointestinal Stromal Tumors1CTD_human
HgeneCTNNA1C1837029Macular Dystrophy, Butterfly-Shaped Pigmentary, 21CTD_human;UNIPROT
HgeneCTNNA1C1868569Patterned dystrophy of retinal pigment epithelium1CTD_human
HgeneCTNNA1C1879321Acute Myeloid Leukemia (AML-M2)1CTD_human
HgeneCTNNA1C2713368Hematopoetic Myelodysplasia1CTD_human
HgeneCTNNA1C3179349Gastrointestinal Stromal Sarcoma1CTD_human
HgeneCTNNA1C3463824MYELODYSPLASTIC SYNDROME1CTD_human
HgeneCTNNA1C4511237Butterfly-shaped pigmentary macular dystrophy1ORPHANET
TgeneEGR1C0009171Cocaine Abuse3CTD_human
TgeneEGR1C0236736Cocaine-Related Disorders3CTD_human
TgeneEGR1C0600427Cocaine Dependence3CTD_human
TgeneEGR1C0008372Intrahepatic Cholestasis2CTD_human
TgeneEGR1C0003129Anoxemia1CTD_human
TgeneEGR1C0003130Anoxia1CTD_human
TgeneEGR1C0004364Autoimmune Diseases1CTD_human
TgeneEGR1C0007786Brain Ischemia1CTD_human
TgeneEGR1C0008311Cholangitis1CTD_human
TgeneEGR1C0008370Cholestasis1CTD_human
TgeneEGR1C0020295Hydronephrosis1CTD_human
TgeneEGR1C0021368Inflammation1CTD_human
TgeneEGR1C0022116Ischemia1CTD_human
TgeneEGR1C0024121Lung Neoplasms1CTD_human
TgeneEGR1C0025500Mesothelioma1CTD_human
TgeneEGR1C0032285Pneumonia1CTD_human
TgeneEGR1C0032300Lobar Pneumonia1CTD_human
TgeneEGR1C0033578Prostatic Neoplasms1CTD_human
TgeneEGR1C0035126Reperfusion Injury1CTD_human
TgeneEGR1C0087031Juvenile-Onset Still Disease1CTD_human
TgeneEGR1C0242184Hypoxia1CTD_human
TgeneEGR1C0242379Malignant neoplasm of lung1CTD_human
TgeneEGR1C0376358Malignant neoplasm of prostate1CTD_human
TgeneEGR1C0700292Hypoxemia1CTD_human
TgeneEGR1C0887898Experimental Lung Inflammation1CTD_human
TgeneEGR1C0917798Cerebral Ischemia1CTD_human
TgeneEGR1C2239176Liver carcinoma1CTD_human
TgeneEGR1C3495559Juvenile arthritis1CTD_human
TgeneEGR1C3714636Pneumonitis1CTD_human
TgeneEGR1C3714758Juvenile psoriatic arthritis1CTD_human
TgeneEGR1C4552091Polyarthritis, Juvenile, Rheumatoid Factor Negative1CTD_human
TgeneEGR1C4704862Polyarthritis, Juvenile, Rheumatoid Factor Positive1CTD_human