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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:MAP4K4-TXNL4A

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MAP4K4-TXNL4A
FusionPDB ID: 51416
FusionGDB2.0 ID: 51416
HgeneTgene
Gene symbol

MAP4K4

TXNL4A

Gene ID

9448

10907

Gene namemitogen-activated protein kinase kinase kinase kinase 4thioredoxin like 4A
SynonymsFLH21957|HEL-S-31|HGK|MEKKK4|NIKBMKS|DIB1|DIM1|SNRNP15|TXNL4|U5-15kD
Cytomap

2q11.2

18q23

Type of geneprotein-codingprotein-coding
Descriptionmitogen-activated protein kinase kinase kinase kinase 4HPK/GCK-like kinase HGKMAPK/ERK kinase kinase kinase 4MEK kinase kinase 4Ste20 group protein kinase HGKepididymis secretory protein Li 31hepatocyte progenitor kinase-like/germinal center kinase-thioredoxin-like protein 4ADIM1 protein homologspliceosomal U5 snRNP-specific 15 kDa proteinthioredoxin-like 4thioredoxin-like U5 snRNP protein U5-15kD
Modification date2020031520200313
UniProtAcc

O95819

.
Ensembl transtripts involved in fusion geneENST idsENST00000302217, ENST00000324219, 
ENST00000347699, ENST00000350198, 
ENST00000413150, ENST00000425019, 
ENST00000456652, ENST00000350878, 
ENST00000498066, 
ENST00000585474, 
ENST00000591711, ENST00000592837, 
ENST00000592957, ENST00000588162, 
ENST00000589926, ENST00000269601, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 11 X 9=15847 X 3 X 6=126
# samples 169
** MAII scorelog2(16/1584*10)=-3.30742852519225
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/126*10)=-0.485426827170242
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: MAP4K4 [Title/Abstract] AND TXNL4A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MAP4K4(102407238)-TXNL4A(77737701), # samples:1
Anticipated loss of major functional domain due to fusion event.MAP4K4-TXNL4A 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.
MAP4K4-TXNL4A 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.
* 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
HgeneMAP4K4

GO:0006468

protein phosphorylation

9890973

HgeneMAP4K4

GO:0035556

intracellular signal transduction

9890973

HgeneMAP4K4

GO:0046328

regulation of JNK cascade

14966141

TgeneTXNL4A

GO:0000398

mRNA splicing, via spliceosome

28781166


check buttonFusion gene breakpoints across MAP4K4 (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 TXNL4A (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
ChimerDB4STADTCGA-BR-8366MAP4K4chr2

102407238

+TXNL4Achr18

77737701

-


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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)
ENST00000425019MAP4K4chr2102407238+ENST00000269601TXNL4Achr1877737701-1611517235792185
ENST00000324219MAP4K4chr2102407238+ENST00000269601TXNL4Achr1877737701-13482545529174
ENST00000350198MAP4K4chr2102407238+ENST00000269601TXNL4Achr1877737701-13482545529174
ENST00000302217MAP4K4chr2102407238+ENST00000269601TXNL4Achr1877737701-13482545529174
ENST00000413150MAP4K4chr2102407238+ENST00000269601TXNL4Achr1877737701-132923522510162
ENST00000347699MAP4K4chr2102407238+ENST00000269601TXNL4Achr1877737701-12741800455151
ENST00000456652MAP4K4chr2102407238+ENST00000269601TXNL4Achr1877737701-12741800455151

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
ENST00000425019ENST00000269601MAP4K4chr2102407238+TXNL4Achr1877737701-0.001253830.99874616
ENST00000324219ENST00000269601MAP4K4chr2102407238+TXNL4Achr1877737701-0.0026689870.997331
ENST00000350198ENST00000269601MAP4K4chr2102407238+TXNL4Achr1877737701-0.0026689870.997331
ENST00000302217ENST00000269601MAP4K4chr2102407238+TXNL4Achr1877737701-0.0026689870.997331
ENST00000413150ENST00000269601MAP4K4chr2102407238+TXNL4Achr1877737701-0.001672470.99832755
ENST00000347699ENST00000269601MAP4K4chr2102407238+TXNL4Achr1877737701-0.0019973660.9980026
ENST00000456652ENST00000269601MAP4K4chr2102407238+TXNL4Achr1877737701-0.0019973660.9980026

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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

>51416_51416_1_MAP4K4-TXNL4A_MAP4K4_chr2_102407238_ENST00000302217_TXNL4A_chr18_77737701_ENST00000269601_length(amino acids)=174AA_BP=83
MRLRYTERQRHLLLFVFWWQKGKMANDSPAKSLVDIDLSSLRDPAGIFELVEVVGNGTYGQVYKGRHVKTGQLAAIKVMDVTEVKNFAVI

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

>51416_51416_2_MAP4K4-TXNL4A_MAP4K4_chr2_102407238_ENST00000324219_TXNL4A_chr18_77737701_ENST00000269601_length(amino acids)=174AA_BP=83
MRLRYTERQRHLLLFVFWWQKGKMANDSPAKSLVDIDLSSLRDPAGIFELVEVVGNGTYGQVYKGRHVKTGQLAAIKVMDVTEVKNFAVI

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

>51416_51416_3_MAP4K4-TXNL4A_MAP4K4_chr2_102407238_ENST00000347699_TXNL4A_chr18_77737701_ENST00000269601_length(amino acids)=151AA_BP=60
MANDSPAKSLVDIDLSSLRDPAGIFELVEVVGNGTYGQVYKGRHVKTGQLAAIKVMDVTEVKNFAVIYLVDITEVPDFNKMYELYDPCTV

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

>51416_51416_4_MAP4K4-TXNL4A_MAP4K4_chr2_102407238_ENST00000350198_TXNL4A_chr18_77737701_ENST00000269601_length(amino acids)=174AA_BP=83
MRLRYTERQRHLLLFVFWWQKGKMANDSPAKSLVDIDLSSLRDPAGIFELVEVVGNGTYGQVYKGRHVKTGQLAAIKVMDVTEVKNFAVI

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

>51416_51416_5_MAP4K4-TXNL4A_MAP4K4_chr2_102407238_ENST00000413150_TXNL4A_chr18_77737701_ENST00000269601_length(amino acids)=162AA_BP=71
MLFVFWWQKGKMANDSPAKSLVDIDLSSLRDPAGIFELVEVVGNGTYGQVYKGRHVKTGQLAAIKVMDVTEVKNFAVIYLVDITEVPDFN

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

>51416_51416_6_MAP4K4-TXNL4A_MAP4K4_chr2_102407238_ENST00000425019_TXNL4A_chr18_77737701_ENST00000269601_length(amino acids)=185AA_BP=94
MPREERGRRPGLRLRYTERQRHLLLFVFWWQKGKMANDSPAKSLVDIDLSSLRDPAGIFELVEVVGNGTYGQVYKGRHVKTGQLAAIKVM
DVTEVKNFAVIYLVDITEVPDFNKMYELYDPCTVMFFFRNKHIMIDLGTGNNNKINWAMEDKQEMVDIIETVYRGARKGRGLVVSPKDYS

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

>51416_51416_7_MAP4K4-TXNL4A_MAP4K4_chr2_102407238_ENST00000456652_TXNL4A_chr18_77737701_ENST00000269601_length(amino acids)=151AA_BP=60
MANDSPAKSLVDIDLSSLRDPAGIFELVEVVGNGTYGQVYKGRHVKTGQLAAIKVMDVTEVKNFAVIYLVDITEVPDFNKMYELYDPCTV

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

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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/chr2:102407238/chr18:77737701)
- 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
MAP4K4

O95819

.
FUNCTION: Serine/threonine kinase that may play a role in the response to environmental stress and cytokines such as TNF-alpha. Appears to act upstream of the JUN N-terminal pathway. Phosphorylates SMAD1 on Thr-322. {ECO:0000269|PubMed:21690388, ECO:0000269|PubMed:9890973}.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
HgeneMAP4K4chr2:102407238chr18:77737701ENST00000347699+33031_3960.01240.0Nucleotide bindingATP

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMAP4K4chr2:102407238chr18:77737701ENST00000347699+33025_28960.01240.0DomainProtein kinase
HgeneMAP4K4chr2:102407238chr18:77737701ENST00000347699+330926_121360.01240.0DomainCNH


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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
MAP4K4
TXNL4A


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 MAP4K4-TXNL4A


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 MAP4K4-TXNL4A


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