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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:MTHFS-BCL2A1 (FusionGDB2 ID:55696)

Fusion Gene Summary for MTHFS-BCL2A1

check button Fusion gene summary
Fusion gene informationFusion gene name: MTHFS-BCL2A1
Fusion gene ID: 55696
HgeneTgene
Gene symbol

MTHFS

BCL2A1

Gene ID

100528021

597

Gene nameST20-MTHFS readthroughBCL2 related protein A1
SynonymsMTHFSACC-1|ACC-2|ACC1|ACC2|BCL2L5|BFL1|GRS|HBPA1
Cytomap

15q25.1

15q25.1

Type of geneprotein-codingprotein-coding
DescriptionST20-MTHFS protein5,10-methenyl-tetrahydrofolate synthetase5-formyltetrahydrofolate cyclo-ligaseMethenyl-THF synthetasebcl-2-related protein A1bcl-2-like protein 5bcl2-L-5hematopoietic BCL2-related protein A1hemopoietic-specific early response proteinprotein BFL-1
Modification date2020031320200313
UniProtAcc.

Q16548

Ensembl transtripts involved in fusion geneENST00000258874, ENST00000559722, 
ENST00000267953, ENST00000335661, 
Fusion gene scores* DoF score3 X 3 X 2=184 X 1 X 4=16
# samples 46
** MAII scorelog2(4/18*10)=1.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(6/16*10)=1.90689059560852
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MTHFS [Title/Abstract] AND BCL2A1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMTHFS(80181435)-BCL2A1(80253516), # samples:6
Anticipated loss of major functional domain due to fusion event.MTHFS-BCL2A1 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

check buttonFusion gene breakpoints across MTHFS (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across BCL2A1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4KIRCTCGA-B0-4700-01AMTHFSchr15

80181435

-BCL2A1chr15

80253516

-
ChimerDB4LIHCTCGA-BC-A3KG-01AMTHFSchr15

80181435

-BCL2A1chr15

80253516

-
ChimerDB4LIHCTCGA-DD-A73G-01AMTHFSchr15

80181435

-BCL2A1chr15

80253516

-
ChimerDB4LIHCTCGA-DD-A73GMTHFSchr15

80189213

-BCL2A1chr15

80253516

-
ChimerDB4LIHCTCGA-DD-AAD6-01AMTHFSchr15

80181435

-BCL2A1chr15

80253516

-
ChimerDB4LIHCTCGA-DD-AAD6MTHFSchr15

80181435

-BCL2A1chr15

80253516

-
ChimerDB4LIHCTCGA-DD-AAD6MTHFSchr15

80189214

-BCL2A1chr15

80253516

-


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Fusion Gene ORF analysis for MTHFS-BCL2A1

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-shiftENST00000258874ENST00000267953MTHFSchr15

80181435

-BCL2A1chr15

80253516

-
Frame-shiftENST00000258874ENST00000335661MTHFSchr15

80181435

-BCL2A1chr15

80253516

-
In-frameENST00000258874ENST00000267953MTHFSchr15

80189213

-BCL2A1chr15

80253516

-
In-frameENST00000258874ENST00000267953MTHFSchr15

80189214

-BCL2A1chr15

80253516

-
In-frameENST00000258874ENST00000335661MTHFSchr15

80189213

-BCL2A1chr15

80253516

-
In-frameENST00000258874ENST00000335661MTHFSchr15

80189214

-BCL2A1chr15

80253516

-
In-frameENST00000559722ENST00000267953MTHFSchr15

80181435

-BCL2A1chr15

80253516

-
In-frameENST00000559722ENST00000335661MTHFSchr15

80181435

-BCL2A1chr15

80253516

-
intron-3CDSENST00000559722ENST00000267953MTHFSchr15

80189213

-BCL2A1chr15

80253516

-
intron-3CDSENST00000559722ENST00000267953MTHFSchr15

80189214

-BCL2A1chr15

80253516

-
intron-3CDSENST00000559722ENST00000335661MTHFSchr15

80189213

-BCL2A1chr15

80253516

-
intron-3CDSENST00000559722ENST00000335661MTHFSchr15

80189214

-BCL2A1chr15

80253516

-

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 MTHFS-BCL2A1


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)

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.
genomic feature

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 MTHFS-BCL2A1


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/chr15:80181435/chr15:80253516)
- 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
.BCL2A1

Q16548

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: Retards apoptosis induced by IL-3 deprivation. May function in the response of hemopoietic cells to external signals and in maintaining endothelial survival during infection (By similarity). Can inhibit apoptosis induced by serum starvation in the mammary epithelial cell line HC11 (By similarity). {ECO:0000250, ECO:0000250|UniProtKB:Q07440}.

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
HgeneMTHFSchr15:80181435chr15:80253516ENST00000258874-2310_14126204.0Nucleotide bindingNote=ATP
HgeneMTHFSchr15:80189213chr15:80253516ENST00000258874-1310_1439204.0Nucleotide bindingNote=ATP
HgeneMTHFSchr15:80189214chr15:80253516ENST00000258874-1310_1439204.0Nucleotide bindingNote=ATP

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMTHFSchr15:80181435chr15:80253516ENST00000258874-23145_153126204.0Nucleotide bindingNote=ATP
HgeneMTHFSchr15:80189213chr15:80253516ENST00000258874-13145_15339204.0Nucleotide bindingNote=ATP
HgeneMTHFSchr15:80189214chr15:80253516ENST00000258874-13145_15339204.0Nucleotide bindingNote=ATP
HgeneMTHFSchr15:80181435chr15:80253516ENST00000258874-23148_152126204.0RegionNote=Substrate binding
HgeneMTHFSchr15:80189213chr15:80253516ENST00000258874-13148_15239204.0RegionNote=Substrate binding
HgeneMTHFSchr15:80189214chr15:80253516ENST00000258874-13148_15239204.0RegionNote=Substrate binding
TgeneBCL2A1chr15:80181435chr15:80253516ENST000002679530224_33140176.0Compositional biasNote=Ala/Pro-rich
TgeneBCL2A1chr15:80181435chr15:80253516ENST000003356611324_33158164.0Compositional biasNote=Ala/Pro-rich
TgeneBCL2A1chr15:80189213chr15:80253516ENST000002679530224_33140176.0Compositional biasNote=Ala/Pro-rich
TgeneBCL2A1chr15:80189213chr15:80253516ENST000003356611324_33158164.0Compositional biasNote=Ala/Pro-rich
TgeneBCL2A1chr15:80189214chr15:80253516ENST000002679530224_33140176.0Compositional biasNote=Ala/Pro-rich
TgeneBCL2A1chr15:80189214chr15:80253516ENST000003356611324_33158164.0Compositional biasNote=Ala/Pro-rich
TgeneBCL2A1chr15:80181435chr15:80253516ENST0000026795302132_147140176.0MotifNote=BH2
TgeneBCL2A1chr15:80181435chr15:80253516ENST000002679530277_97140176.0MotifNote=BH1
TgeneBCL2A1chr15:80181435chr15:80253516ENST0000033566113132_147158164.0MotifNote=BH2
TgeneBCL2A1chr15:80181435chr15:80253516ENST000003356611377_97158164.0MotifNote=BH1
TgeneBCL2A1chr15:80189213chr15:80253516ENST0000026795302132_147140176.0MotifNote=BH2
TgeneBCL2A1chr15:80189213chr15:80253516ENST000002679530277_97140176.0MotifNote=BH1
TgeneBCL2A1chr15:80189213chr15:80253516ENST0000033566113132_147158164.0MotifNote=BH2
TgeneBCL2A1chr15:80189213chr15:80253516ENST000003356611377_97158164.0MotifNote=BH1
TgeneBCL2A1chr15:80189214chr15:80253516ENST0000026795302132_147140176.0MotifNote=BH2
TgeneBCL2A1chr15:80189214chr15:80253516ENST000002679530277_97140176.0MotifNote=BH1
TgeneBCL2A1chr15:80189214chr15:80253516ENST0000033566113132_147158164.0MotifNote=BH2
TgeneBCL2A1chr15:80189214chr15:80253516ENST000003356611377_97158164.0MotifNote=BH1


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Fusion Gene Sequence for MTHFS-BCL2A1


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 MTHFS-BCL2A1


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 MTHFS-BCL2A1


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 MTHFS-BCL2A1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource