Fusion Gene Studies
in Kim Lab

FusionBase FusionGDB FusionGDB2 FusionPDB FusionNeoAntigen FusionAI FusionNW FGviewer Publication Contact
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:MXD1-ANXA1 (FusionGDB2 ID:HG4084TG301)

Fusion Gene Summary for MXD1-ANXA1

check button Fusion gene summary
Fusion gene informationFusion gene name: MXD1-ANXA1
Fusion gene ID: hg4084tg301
HgeneTgene
Gene symbol

MXD1

ANXA1

Gene ID

4084

301

Gene nameMAX dimerization protein 1annexin A1
SynonymsBHLHC58|MAD|MAD1ANX1|LPC1
Cytomap('MXD1')('ANXA1')

2p13.3

9q21.13

Type of geneprotein-codingprotein-coding
Descriptionmax dimerization protein 1MAX-binding proteinantagonizer of myc transcriptional activitymax dimerizer 1annexin A1annexin I (lipocortin I)annexin-1calpactin IIcalpactin-2chromobindin-9epididymis secretory sperm binding proteinphospholipase A2 inhibitory protein
Modification date2020031320200329
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000264444, ENST00000465446, 
ENST00000540449, 
Fusion gene scores* DoF score7 X 7 X 3=14724 X 6 X 7=1008
# samples 823
** MAII scorelog2(8/147*10)=-0.877744249949002
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(23/1008*10)=-2.13178987255554
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MXD1 [Title/Abstract] AND ANXA1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMXD1(70151710)-ANXA1(75781035), # samples:2
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
HgeneMXD1

GO:0000122

negative regulation of transcription by RNA polymerase II

10723141|12837246

TgeneANXA1

GO:0002548

monocyte chemotaxis

15187149

TgeneANXA1

GO:0007187

G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger

25664854

TgeneANXA1

GO:0008360

regulation of cell shape

15187149

TgeneANXA1

GO:0018149

peptide cross-linking

10908733

TgeneANXA1

GO:0030216

keratinocyte differentiation

10908733

TgeneANXA1

GO:0031340

positive regulation of vesicle fusion

2138016

TgeneANXA1

GO:0031532

actin cytoskeleton reorganization

15187149

TgeneANXA1

GO:0032743

positive regulation of interleukin-2 production

17008549

TgeneANXA1

GO:0035924

cellular response to vascular endothelial growth factor stimulus

22773844

TgeneANXA1

GO:0042102

positive regulation of T cell proliferation

17008549

TgeneANXA1

GO:0045627

positive regulation of T-helper 1 cell differentiation

17008549

TgeneANXA1

GO:0045629

negative regulation of T-helper 2 cell differentiation

17008549

TgeneANXA1

GO:0071385

cellular response to glucocorticoid stimulus

2936963

TgeneANXA1

GO:0071621

granulocyte chemotaxis

15187149

TgeneANXA1

GO:0090050

positive regulation of cell migration involved in sprouting angiogenesis

22773844

TgeneANXA1

GO:0090303

positive regulation of wound healing

25664854



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/AAX186392MXD1chr2

70151710

-ANXA1chr9

75781035

-
ChiTaRS5.0N/AAX187942MXD1chr2

70151710

-ANXA1chr9

75781035

-


Top

Fusion Gene ORF analysis for MXD1-ANXA1

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-3CDSENST00000264444ENST00000257497MXD1chr2

70151710

-ANXA1chr9

75781035

-
intron-3CDSENST00000264444ENST00000376911MXD1chr2

70151710

-ANXA1chr9

75781035

-
intron-3CDSENST00000465446ENST00000257497MXD1chr2

70151710

-ANXA1chr9

75781035

-
intron-3CDSENST00000465446ENST00000376911MXD1chr2

70151710

-ANXA1chr9

75781035

-
intron-3CDSENST00000540449ENST00000257497MXD1chr2

70151710

-ANXA1chr9

75781035

-
intron-3CDSENST00000540449ENST00000376911MXD1chr2

70151710

-ANXA1chr9

75781035

-
intron-intronENST00000264444ENST00000491192MXD1chr2

70151710

-ANXA1chr9

75781035

-
intron-intronENST00000465446ENST00000491192MXD1chr2

70151710

-ANXA1chr9

75781035

-
intron-intronENST00000540449ENST00000491192MXD1chr2

70151710

-ANXA1chr9

75781035

-

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

Top

Fusion Genomic Features for MXD1-ANXA1


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)


Top

Fusion Protein Features for MXD1-ANXA1


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/:70151710/:75781035)
- 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


Top

Fusion Gene Sequence for MXD1-ANXA1


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.

Top

Fusion Gene PPI Analysis for MXD1-ANXA1


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


Top

Related Drugs for MXD1-ANXA1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

Related Diseases for MXD1-ANXA1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMXD1C0162820Dermatitis, Allergic Contact1CTD_human
TgeneC0024667Animal Mammary Neoplasms3CTD_human
TgeneC1257925Mammary Carcinoma, Animal3CTD_human
TgeneC0007097Carcinoma2CTD_human
TgeneC0024668Mammary Neoplasms, Experimental2CTD_human
TgeneC0205696Anaplastic carcinoma2CTD_human
TgeneC0205697Carcinoma, Spindle-Cell2CTD_human
TgeneC0205698Undifferentiated carcinoma2CTD_human
TgeneC0205699Carcinomatosis2CTD_human
TgeneC0007137Squamous cell carcinoma1CTD_human
TgeneC0020538Hypertensive disease1CTD_human
TgeneC0022658Kidney Diseases1CTD_human
TgeneC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneC0024232Lymphatic Metastasis1CTD_human
TgeneC0026640Mouth Neoplasms1CTD_human
TgeneC0027626Neoplasm Invasiveness1CTD_human
TgeneC0027627Neoplasm Metastasis1CTD_human
TgeneC0033578Prostatic Neoplasms1CTD_human
TgeneC0038354Stomach Diseases1CTD_human
TgeneC0152013Adenocarcinoma of lung (disorder)1CTD_human
TgeneC0153381Malignant neoplasm of mouth1CTD_human
TgeneC0279626Squamous cell carcinoma of esophagus1CTD_human
TgeneC0376358Malignant neoplasm of prostate1CTD_human
TgeneC0376634Craniofacial Abnormalities1CTD_human