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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:L3MBTL4-TRDMT1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: L3MBTL4-TRDMT1
FusionPDB ID: 43810
FusionGDB2.0 ID: 43810
HgeneTgene
Gene symbol

L3MBTL4

TRDMT1

Gene ID

91133

1787

Gene nameL3MBTL histone methyl-lysine binding protein 4tRNA aspartic acid methyltransferase 1
SynonymsHsT1031DMNT2|DNMT2|MHSAIIP|PUMET|RNMT1
Cytomap

18p11.31

10p13

Type of geneprotein-codingprotein-coding
Descriptionlethal(3)malignant brain tumor-like protein 4H-l(3)mbt-like protein 4L3MBTL4, histone methyl-lysine binding proteintRNA (cytosine(38)-C(5))-methyltransferaseDNA (cytosine-5)-methyltransferase-like protein 2DNA MTase homolog HsaIIPDNA cytosine-5 methyltransferase 2DNA methyltransferase-2tRNA (cytosine-5-)-methyltransferase
Modification date2020031320200313
UniProtAcc

Q8NA19

.
Ensembl transtripts involved in fusion geneENST idsENST00000284898, ENST00000317931, 
ENST00000400104, ENST00000400105, 
ENST00000535782, ENST00000578677, 
ENST00000457442, ENST00000452380, 
ENST00000488990, ENST00000351358, 
ENST00000358282, ENST00000377766, 
ENST00000377799, ENST00000412821, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 8 X 4=2563 X 3 X 2=18
# samples 83
** MAII scorelog2(8/256*10)=-1.67807190511264
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: L3MBTL4 [Title/Abstract] AND TRDMT1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)L3MBTL4(6237963)-TRDMT1(17216659), # samples:2
Anticipated loss of major functional domain due to fusion event.L3MBTL4-TRDMT1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
L3MBTL4-TRDMT1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
L3MBTL4-TRDMT1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
L3MBTL4-TRDMT1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
L3MBTL4-TRDMT1 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
L3MBTL4-TRDMT1 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
L3MBTL4-TRDMT1 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
L3MBTL4-TRDMT1 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism 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
TgeneTRDMT1

GO:0030488

tRNA methylation

16424344


check buttonFusion gene breakpoints across L3MBTL4 (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 TRDMT1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4BLCATCGA-ZF-AA4T-01AL3MBTL4chr18

6237963

-TRDMT1chr10

17216659

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000535782L3MBTL4chr186237963-ENST00000377799TRDMT1chr1017216659-368927401385461
ENST00000535782L3MBTL4chr186237963-ENST00000412821TRDMT1chr1017216659-147727401313437
ENST00000535782L3MBTL4chr186237963-ENST00000351358TRDMT1chr1017216659-141127401247415

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
ENST00000535782ENST00000377799L3MBTL4chr186237963-TRDMT1chr1017216659-0.0001526850.9998473
ENST00000535782ENST00000412821L3MBTL4chr186237963-TRDMT1chr1017216659-0.0003523080.99964774
ENST00000535782ENST00000351358L3MBTL4chr186237963-TRDMT1chr1017216659-0.0002278110.99977225

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>43810_43810_1_L3MBTL4-TRDMT1_L3MBTL4_chr18_6237963_ENST00000535782_TRDMT1_chr10_17216659_ENST00000351358_length(amino acids)=415AA_BP=91
LQNAPKKLFRNRSPNGPMSKEFQVGMKLEAVDRKNPSLVCVATIADIVEDRLLVHFDNWDDSYDYWCDVNSPYVQPVGWCQENGRTLIAP
QESCIPAQVVAAIDVNTVANEVYKYNFPHTQLLAKTIEGITLEEFDRLSFDMILMSPPCQPFTRDLLIQTIENCGFQYQEFLLSPTSLGI
PNSRLRYFLIAKLQSEPLPFQAPGQVLMEFPKIESVHPQKYAMDVENKIQEKNVEPNISFDGSIQCSGKDAILFKLETAEEIHRKNQQDS
DLSVKMLKDFLEDDTDVNQYLLPPKSLLRYALLLDIVQPTCRRSVCFTKGYGSYIEGTGSVLQTAEDVQVENIYKSLTNLSQEEQITKLL

--------------------------------------------------------------

>43810_43810_2_L3MBTL4-TRDMT1_L3MBTL4_chr18_6237963_ENST00000535782_TRDMT1_chr10_17216659_ENST00000377799_length(amino acids)=461AA_BP=91
LQNAPKKLFRNRSPNGPMSKEFQVGMKLEAVDRKNPSLVCVATIADIVEDRLLVHFDNWDDSYDYWCDVNSPYVQPVGWCQENGRTLIAP
QESCIPAQVVAAIDVNTVANEVYKYNFPHTQLLAKTIEGITLEEFDRLSFDMILMSPPCQPFTRIGRQGDMTDSRTNSFLHILDILPRLQ
KLPKYILLENVKGFEVSSTRDLLIQTIENCGFQYQEFLLSPTSLGIPNSRLRYFLIAKLQSEPLPFQAPGQVLMEFPKIESVHPQKYAMD
VENKIQEKNVEPNISFDGSIQCSGKDAILFKLETAEEIHRKNQQDSDLSVKMLKDFLEDDTDVNQYLLPPKSLLRYALLLDIVQPTCRRS
VCFTKGYGSYIEGTGSVLQTAEDVQVENIYKSLTNLSQEEQITKLLILKLRYFTPKEIANLLGFPPEFGFPEKITVKQRYRLLGNSLNVH

--------------------------------------------------------------

>43810_43810_3_L3MBTL4-TRDMT1_L3MBTL4_chr18_6237963_ENST00000535782_TRDMT1_chr10_17216659_ENST00000412821_length(amino acids)=437AA_BP=91
LQNAPKKLFRNRSPNGPMSKEFQVGMKLEAVDRKNPSLVCVATIADIVEDRLLVHFDNWDDSYDYWCDVNSPYVQPVGWCQENGRTLIAP
QESCIPAQVVAAIDVNTVANEVYKYNFPHTQLLAKTIEGITLEEFDRLSFDMILMSPPCQPFTRLQKLPKYILLENVKGFEVSSTRDLLI
QTIENCGFQYQEFLLSPTSLGIPNSRLRYFLIAKLQSEPLPFQAPGQVLMEFPKIESVHPQKYAMDVENKIQEKNVEPNISFDGSIQCSG
KDAILFKLETAEEIHRKNQQDSDLSVKMLKDFLEDDTDVNQYLLPPKSLLRYALLLDIVQPTCRRSVCFTKGYGSYIEGTGSVLQTAEDV

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr18:6237963/chr10:17216659)
- 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
L3MBTL4

Q8NA19

.
FUNCTION: Putative Polycomb group (PcG) protein. PcG proteins maintain the transcriptionally repressive state of genes, probably via a modification of chromatin, rendering it heritably changed in its expressibility (By similarity). {ECO:0000250}.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.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000284898-1020160_260261.3333333333333624.0RepeatNote=MBT 2
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000284898-102052_152261.3333333333333624.0RepeatNote=MBT 1
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000400104-1017160_260261.3333333333333535.0RepeatNote=MBT 2
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000400104-101752_152261.3333333333333535.0RepeatNote=MBT 1
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000400105-1020160_260261.3333333333333624.0RepeatNote=MBT 2
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000400105-102052_152261.3333333333333624.0RepeatNote=MBT 1
TgeneTRDMT1chr18:6237963chr10:17216659ENST000003513580957_5821.333333333333332346.0RegionS-adenosyl-L-methionine binding
TgeneTRDMT1chr18:6237963chr10:17216659ENST000003582820957_5821.333333333333332143.0RegionS-adenosyl-L-methionine binding
TgeneTRDMT1chr18:6237963chr10:17216659ENST0000037779901157_5821.333333333333332392.0RegionS-adenosyl-L-methionine binding
TgeneTRDMT1chr18:6237963chr10:17216659ENST0000041282101057_5821.333333333333332368.0RegionS-adenosyl-L-methionine binding

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000284898-1020543_607261.3333333333333624.0DomainSAM
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000400104-1017543_607261.3333333333333535.0DomainSAM
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000400105-1020543_607261.3333333333333624.0DomainSAM
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000284898-1020269_364261.3333333333333624.0RepeatNote=MBT 3
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000400104-1017269_364261.3333333333333535.0RepeatNote=MBT 3
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000400105-1020269_364261.3333333333333624.0RepeatNote=MBT 3
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000284898-1020370_414261.3333333333333624.0Zinc fingerCCHHC-type
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000400104-1017370_414261.3333333333333535.0Zinc fingerCCHHC-type
HgeneL3MBTL4chr18:6237963chr10:17216659ENST00000400105-1020370_414261.3333333333333624.0Zinc fingerCCHHC-type
TgeneTRDMT1chr18:6237963chr10:17216659ENST00000351358094_39121.333333333333332346.0DomainSAM-dependent MTase C5-type
TgeneTRDMT1chr18:6237963chr10:17216659ENST00000358282094_39121.333333333333332143.0DomainSAM-dependent MTase C5-type
TgeneTRDMT1chr18:6237963chr10:17216659ENST000003777990114_39121.333333333333332392.0DomainSAM-dependent MTase C5-type
TgeneTRDMT1chr18:6237963chr10:17216659ENST000004128210104_39121.333333333333332368.0DomainSAM-dependent MTase C5-type
TgeneTRDMT1chr18:6237963chr10:17216659ENST000003513580913_1521.333333333333332346.0RegionS-adenosyl-L-methionine binding
TgeneTRDMT1chr18:6237963chr10:17216659ENST000003582820913_1521.333333333333332143.0RegionS-adenosyl-L-methionine binding
TgeneTRDMT1chr18:6237963chr10:17216659ENST0000037779901113_1521.333333333333332392.0RegionS-adenosyl-L-methionine binding
TgeneTRDMT1chr18:6237963chr10:17216659ENST0000041282101013_1521.333333333333332368.0RegionS-adenosyl-L-methionine binding


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
L3MBTL4
TRDMT1


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to L3MBTL4-TRDMT1


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to L3MBTL4-TRDMT1


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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