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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:DHFR-ZMYM4 (FusionGDB2 ID:HG1719TG9202)

Fusion Gene Summary for DHFR-ZMYM4

check button Fusion gene summary
Fusion gene informationFusion gene name: DHFR-ZMYM4
Fusion gene ID: hg1719tg9202
HgeneTgene
Gene symbol

DHFR

ZMYM4

Gene ID

1719

9202

Gene namedihydrofolate reductasezinc finger MYM-type containing 4
SynonymsDHFRP1|DYRCDIR|MYM|ZNF198L3|ZNF262
Cytomap('DHFR')('ZMYM4')

5q14.1

1p34.3

Type of geneprotein-codingprotein-coding
Descriptiondihydrofolate reductasezinc finger MYM-type protein 4cell death inhibiting RNAzinc finger protein 262zinc finger, MYM-type 4
Modification date2020031520200313
UniProtAcc

P00374

.
Ensembl transtripts involved in fusion geneENST00000439211, ENST00000504396, 
ENST00000505337, ENST00000511032, 
ENST00000513048, 
Fusion gene scores* DoF score8 X 8 X 1=6413 X 13 X 7=1183
# samples 814
** MAII scorelog2(8/64*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(14/1183*10)=-3.07895134139482
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DHFR [Title/Abstract] AND ZMYM4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDHFR(79947559)-ZMYM4(35826572), # 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
HgeneDHFR

GO:0017148

negative regulation of translation

8490020

HgeneDHFR

GO:0046452

dihydrofolate metabolic process

2303423|23707606

HgeneDHFR

GO:0046653

tetrahydrofolate metabolic process

12096917|21876184

HgeneDHFR

GO:0046654

tetrahydrofolate biosynthetic process

2303423

HgeneDHFR

GO:0055114

oxidation-reduction process

23707606



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


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Fusion Gene ORF analysis for DHFR-ZMYM4

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

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 DHFR-ZMYM4


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)


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Fusion Protein Features for DHFR-ZMYM4


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/:79947559/:35826572)
- 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
DHFR

P00374

.
FUNCTION: Key enzyme in folate metabolism. Contributes to the de novo mitochondrial thymidylate biosynthesis pathway. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis. Binds its own mRNA and that of DHFR2. {ECO:0000269|PubMed:12096917, ECO:0000269|PubMed:21876188}.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 DHFR-ZMYM4


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 DHFR-ZMYM4


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 DHFR-ZMYM4


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneDHFRP00374DB00563MethotrexateInhibitorSmall moleculeApproved
HgeneDHFRP00374DB01131ProguanilInhibitorSmall moleculeApproved
HgeneDHFRP00374DB00642PemetrexedInhibitorSmall moleculeApproved|Investigational
HgeneDHFRP00374DB01157TrimetrexateInhibitorSmall moleculeApproved|Investigational
HgeneDHFRP00374DB06813PralatrexateInhibitorSmall moleculeApproved|Investigational
HgeneDHFRP00374DB00205PyrimethamineInhibitorSmall moleculeApproved|Investigational|Vet_approved
HgeneDHFRP00374DB00157NADHSmall moleculeApproved|Nutraceutical
HgeneDHFRP00374DB00798GentamicinSmall moleculeApproved|Vet_approved

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Related Diseases for DHFR-ZMYM4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDHFRC3151205Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency4CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneDHFRC0002888Anemia, Megaloblastic2CTD_human
HgeneDHFRC0006142Malignant neoplasm of breast2CTD_human
HgeneDHFRC0025521Inborn Errors of Metabolism2CTD_human
HgeneDHFRC0027765nervous system disorder2CTD_human
HgeneDHFRC0268608Deficiency of dihydrofolate reductase2GENOMICS_ENGLAND
HgeneDHFRC0678222Breast Carcinoma2CTD_human
HgeneDHFRC1257931Mammary Neoplasms, Human2CTD_human
HgeneDHFRC1458155Mammary Neoplasms2CTD_human
HgeneDHFRC4704874Mammary Carcinoma, Human2CTD_human
HgeneDHFRC0000786Spontaneous abortion1CTD_human
HgeneDHFRC0000822Abortion, Tubal1CTD_human
HgeneDHFRC0003873Rheumatoid Arthritis1CTD_human
HgeneDHFRC0004352Autistic Disorder1CTD_human
HgeneDHFRC0009402Colorectal Carcinoma1CTD_human
HgeneDHFRC0009404Colorectal Neoplasms1CTD_human
HgeneDHFRC0013221Drug toxicity1CTD_human
HgeneDHFRC0016412Folic Acid Deficiency1CTD_human
HgeneDHFRC0019193Hepatitis, Toxic1CTD_human
HgeneDHFRC0021361Female infertility1CTD_human
HgeneDHFRC0027627Neoplasm Metastasis1CTD_human
HgeneDHFRC0029463Osteosarcoma1CTD_human
HgeneDHFRC0030312Pancytopenia1CTD_human
HgeneDHFRC0038279Sterility, Postpartum1CTD_human
HgeneDHFRC0041755Adverse reaction to drug1CTD_human
HgeneDHFRC0341869Subfertility, Female1CTD_human
HgeneDHFRC0860207Drug-Induced Liver Disease1CTD_human
HgeneDHFRC0917730Female sterility1CTD_human
HgeneDHFRC1262760Hepatitis, Drug-Induced1CTD_human
HgeneDHFRC3658290Drug-Induced Acute Liver Injury1CTD_human
HgeneDHFRC3830362Early Pregnancy Loss1CTD_human
HgeneDHFRC4277682Chemical and Drug Induced Liver Injury1CTD_human
HgeneDHFRC4279912Chemically-Induced Liver Toxicity1CTD_human
HgeneDHFRC4552766Miscarriage1CTD_human