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:TMED4-ENG (FusionGDB2 ID:91461)

Fusion Gene Summary for TMED4-ENG

check button Fusion gene summary
Fusion gene informationFusion gene name: TMED4-ENG
Fusion gene ID: 91461
HgeneTgene
Gene symbol

TMED4

ENG

Gene ID

222068

2022

Gene nametransmembrane p24 trafficking protein 4endoglin
SynonymsERS25|GMP25iso|HNLF|p24a3|p24alpha3END|HHT1|ORW1
Cytomap

7p13

9q34.11

Type of geneprotein-codingprotein-coding
Descriptiontransmembrane emp24 domain-containing protein 4endoplasmic reticulum stress-response protein 25 kDap24 family protein alpha-3putative NF-kappa-B-activating protein 156putative NFkB activating protein HNLFtransmembrane emp24 protein transport domain cendoglinCD105 antigen
Modification date2020032020200329
UniProtAcc.

Q8NFI3

Ensembl transtripts involved in fusion geneENST00000444131, ENST00000457408, 
ENST00000289577, ENST00000481238, 
ENST00000480266, ENST00000344849, 
ENST00000373203, 
Fusion gene scores* DoF score3 X 2 X 1=66 X 7 X 4=168
# samples 36
** MAII scorelog2(3/6*10)=2.32192809488736log2(6/168*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TMED4 [Title/Abstract] AND ENG [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTMED4(44620692)-ENG(130581112), # samples:1
Anticipated loss of major functional domain due to fusion event.TMED4-ENG seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
TgeneENG

GO:0001934

positive regulation of protein phosphorylation

12015308

TgeneENG

GO:0010862

positive regulation of pathway-restricted SMAD protein phosphorylation

12015308

TgeneENG

GO:0017015

regulation of transforming growth factor beta receptor signaling pathway

15702480

TgeneENG

GO:0030336

negative regulation of cell migration

19736306

TgeneENG

GO:0030513

positive regulation of BMP signaling pathway

17068149

TgeneENG

GO:0031953

negative regulation of protein autophosphorylation

12015308


check buttonFusion gene breakpoints across TMED4 (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 ENG (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
ChiTaRS5.0N/AAK123738TMED4chr7

44620692

-ENGchr9

130581112

-


Top

Fusion Gene ORF analysis for TMED4-ENG

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
5CDS-intronENST00000444131ENST00000480266TMED4chr7

44620692

-ENGchr9

130581112

-
5CDS-intronENST00000457408ENST00000480266TMED4chr7

44620692

-ENGchr9

130581112

-
Frame-shiftENST00000444131ENST00000344849TMED4chr7

44620692

-ENGchr9

130581112

-
Frame-shiftENST00000444131ENST00000373203TMED4chr7

44620692

-ENGchr9

130581112

-
In-frameENST00000457408ENST00000344849TMED4chr7

44620692

-ENGchr9

130581112

-
In-frameENST00000457408ENST00000373203TMED4chr7

44620692

-ENGchr9

130581112

-
intron-3CDSENST00000289577ENST00000344849TMED4chr7

44620692

-ENGchr9

130581112

-
intron-3CDSENST00000289577ENST00000373203TMED4chr7

44620692

-ENGchr9

130581112

-
intron-3CDSENST00000481238ENST00000344849TMED4chr7

44620692

-ENGchr9

130581112

-
intron-3CDSENST00000481238ENST00000373203TMED4chr7

44620692

-ENGchr9

130581112

-
intron-intronENST00000289577ENST00000480266TMED4chr7

44620692

-ENGchr9

130581112

-
intron-intronENST00000481238ENST00000480266TMED4chr7

44620692

-ENGchr9

130581112

-

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)
ENST00000457408TMED4chr744620692-ENST00000373203ENGchr9130581112-1923587531252399
ENST00000457408TMED4chr744620692-ENST00000344849ENGchr9130581112-2054587531153366

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
ENST00000457408ENST00000373203TMED4chr744620692-ENGchr9130581112-0.0514675830.9485324
ENST00000457408ENST00000344849TMED4chr744620692-ENGchr9130581112-0.0278660340.97213393

Top

Fusion Genomic Features for TMED4-ENG


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.

Top

Fusion Protein Features for TMED4-ENG


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/chr7:44620692/chr9:130581112)
- 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
.ENG

Q8NFI3

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: Endoglycosidase that releases N-glycans from glycoproteins by cleaving the beta-1,4-glycosidic bond in the N,N'-diacetylchitobiose core. Involved in the processing of free oligosaccharides in the cytosol. {ECO:0000269|PubMed:12114544}.

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
HgeneTMED4chr7:44620692chr9:130581112ENST00000457408-45147_176178228.0Coiled coilOntology_term=ECO:0000255
HgeneTMED4chr7:44620692chr9:130581112ENST00000457408-4539_137178228.0DomainGOLD
TgeneENGchr7:44620692chr9:130581112ENST00000344849914612_658437626.0Topological domainCytoplasmic
TgeneENGchr7:44620692chr9:130581112ENST00000373203915612_658437659.0Topological domainCytoplasmic
TgeneENGchr7:44620692chr9:130581112ENST00000344849914587_611437626.0TransmembraneHelical
TgeneENGchr7:44620692chr9:130581112ENST00000373203915587_611437659.0TransmembraneHelical

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneTMED4chr7:44620692chr9:130581112ENST00000481238-14147_1760187.0Coiled coilOntology_term=ECO:0000255
HgeneTMED4chr7:44620692chr9:130581112ENST00000481238-1439_1370187.0DomainGOLD
HgeneTMED4chr7:44620692chr9:130581112ENST00000457408-45220_221178228.0MotifCOPII vesicle coat-binding
HgeneTMED4chr7:44620692chr9:130581112ENST00000457408-45220_227178228.0MotifCOPI vesicle coat-binding
HgeneTMED4chr7:44620692chr9:130581112ENST00000481238-14220_2210187.0MotifCOPII vesicle coat-binding
HgeneTMED4chr7:44620692chr9:130581112ENST00000481238-14220_2270187.0MotifCOPI vesicle coat-binding
HgeneTMED4chr7:44620692chr9:130581112ENST00000457408-45213_227178228.0Topological domainCytoplasmic
HgeneTMED4chr7:44620692chr9:130581112ENST00000457408-4530_194178228.0Topological domainLumenal
HgeneTMED4chr7:44620692chr9:130581112ENST00000481238-14213_2270187.0Topological domainCytoplasmic
HgeneTMED4chr7:44620692chr9:130581112ENST00000481238-1430_1940187.0Topological domainLumenal
HgeneTMED4chr7:44620692chr9:130581112ENST00000457408-45195_212178228.0TransmembraneHelical
HgeneTMED4chr7:44620692chr9:130581112ENST00000481238-14195_2120187.0TransmembraneHelical
TgeneENGchr7:44620692chr9:130581112ENST00000344849914336_576437626.0Compositional biasNote=Ser/Thr-rich
TgeneENGchr7:44620692chr9:130581112ENST00000373203915336_576437659.0Compositional biasNote=Ser/Thr-rich
TgeneENGchr7:44620692chr9:130581112ENST00000344849914363_533437626.0DomainZP
TgeneENGchr7:44620692chr9:130581112ENST00000373203915363_533437659.0DomainZP
TgeneENGchr7:44620692chr9:130581112ENST00000344849914399_401437626.0MotifCell attachment site
TgeneENGchr7:44620692chr9:130581112ENST00000373203915399_401437659.0MotifCell attachment site
TgeneENGchr7:44620692chr9:130581112ENST00000344849914200_330437626.0RegionOR1%2C C-terminal part
TgeneENGchr7:44620692chr9:130581112ENST0000034484991426_46437626.0RegionOR1%2C N-terminal part
TgeneENGchr7:44620692chr9:130581112ENST0000034484991447_199437626.0RegionOR2
TgeneENGchr7:44620692chr9:130581112ENST00000373203915200_330437659.0RegionOR1%2C C-terminal part
TgeneENGchr7:44620692chr9:130581112ENST0000037320391526_46437659.0RegionOR1%2C N-terminal part
TgeneENGchr7:44620692chr9:130581112ENST0000037320391547_199437659.0RegionOR2
TgeneENGchr7:44620692chr9:130581112ENST0000034484991426_586437626.0Topological domainExtracellular
TgeneENGchr7:44620692chr9:130581112ENST0000037320391526_586437659.0Topological domainExtracellular


Top

Fusion Gene Sequence for TMED4-ENG


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.
>91461_91461_1_TMED4-ENG_TMED4_chr7_44620692_ENST00000457408_ENG_chr9_130581112_ENST00000344849_length(transcript)=2054nt_BP=587nt
GCAGGCGCAGAGCGATGCGCAAATGTGCGCAGGCGCTTAGGGGCTGAGGCGCGATGGCAGGTGTCGGGGCTGGGCCTCTGCGGGCGATGG
GGCGGCAGGCCCTGCTGCTTCTCGCGCTGTGCGCCACAGGCGCCCAGGGGCTCTACTTCCACATCGGCGAGACCGAGAAGCGCTGTTTCA
TCGAGGAAATCCCCGACGAGACCATGGTCATCGGCAACTATCGTACCCAGATGTGGGATAAGCAGAAGGAGGTCTTCCTGCCCTCGACCC
CTGGCCTGGGCATGCACGTGGAAGTGAAGGACCCCGACGGCAAGGTGGTGCTGTCCCGGCAGTACGGCTCGGAGGGCCGCTTCACGTTCA
CCTCCCACACGCCCGGTGACCATCAAATCTGTCTGCACTCCAATTCTACCAGGATGGCTCTCTTCGCTGGTGGCAAACTGCGGGTGCATC
TCGACATCCAGGTTGGGGAGCATGCCAACAACTACCCTGAGATTGCTGCAAAAGATAAGCTGACGGAGCTACAGCTCCGCGCCCGCCAGT
TGCTTGATCAGGTGGAACAGATTCAGAAGGAGCAGGATTACCAAAGGAAAAAGGTGCACTGCCTCAACATGGACAGCCTCTCTTTCCAGC
TGGGCCTCTACCTCAGCCCACACTTCCTCCAGGCCTCCAACACCATCGAGCCGGGGCAGCAGAGCTTTGTGCAGGTCAGAGTGTCCCCAT
CCGTCTCCGAGTTCCTGCTCCAGTTAGACAGCTGCCACCTGGACTTGGGGCCTGAGGGAGGCACCGTGGAACTCATCCAGGGCCGGGCGG
CCAAGGGCAACTGTGTGAGCCTGCTGTCCCCAAGCCCCGAGGGTGACCCGCGCTTCAGCTTCCTCCTCCACTTCTACACAGTACCCATAC
CCAAAACCGGCACCCTCAGCTGCACGGTAGCCCTGCGTCCCAAGACCGGGTCTCAAGACCAGGAAGTCCATAGGACTGTCTTCATGCGCT
TGAACATCATCAGCCCTGACCTGTCTGGTTGCACAAGCAAAGGCCTCGTCCTGCCCGCCGTGCTGGGCATCACCTTTGGTGCCTTCCTCA
TCGGGGCCCTGCTCACTGCTGCACTCTGGTACATCTACTCGCACACGCGTGAGTACCCCAGGCCCCCACAGTGAGCATGCCGGGCCCCTC
CATCCACCCGGGGGAGCCCAGTGAAGCCTCTGAGGGATTGAGGGGCCCTGGCCAGGACCCTGACCTCCGCCCCTGCCCCCGCTCCCGCTC
CCAGGTTCCCCCAGCAAGCGGGAGCCCGTGGTGGCGGTGGCTGCCCCGGCCTCCTCGGAGAGCAGCAGCACCAACCACAGCATCGGGAGC
ACCCAGAGCACCCCCTGCTCCACCAGCAGCATGGCATAGCCCCGGCCCCCCGCGCTCGCCCAGCAGGAGAGACTGAGCAGCCGCCAGCTG
GGAGCACTGGTGTGAACTCACCCTGGGAGCCAGTCCTCCACTCGACCCAGAATGGAGCCTGCTCTCCGCGCCTACCCTTCCCGCCTCCCT
CTCAGAGGCCTGCTGCCAGTGCAGCCACTGGCTTGGAACACCTTGGGGTCCCTCCACCCCACAGAACCTTCAACCCAGTGGGTCTGGGAT
ATGGCTGCCCAGGAGACAGACCACTTGCCACGCTGTTGTAAAAACCCAAGTCCCTGTCATTTGAACCTGGATCCAGCACTGGTGAACTGA
GCTGGGCAGGAAGGGAGAACTTGAAACAGATTCAGGCCAGCCCAGCCAGGCCAACAGCACCTCCCCGCTGGGAAGAGAAGAGGGCCCAGC
CCAGAGCCACCTGGATCTATCCCTGCGGCCTCCACACCTGAACTTGCCTAACTAACTGGCAGGGGAGACAGGAGCCTAGCGGAGCCCAGC
CTGGGAGCCCAGAGGGTGGCAAGAACAGTGGGCGTTGGGAGCCTAGCTCCTGCCACATGGAGCCCCCTCTGCCGGTCGGGCAGCCAGCAG

>91461_91461_1_TMED4-ENG_TMED4_chr7_44620692_ENST00000457408_ENG_chr9_130581112_ENST00000344849_length(amino acids)=366AA_BP=178
MAGVGAGPLRAMGRQALLLLALCATGAQGLYFHIGETEKRCFIEEIPDETMVIGNYRTQMWDKQKEVFLPSTPGLGMHVEVKDPDGKVVL
SRQYGSEGRFTFTSHTPGDHQICLHSNSTRMALFAGGKLRVHLDIQVGEHANNYPEIAAKDKLTELQLRARQLLDQVEQIQKEQDYQRKK
VHCLNMDSLSFQLGLYLSPHFLQASNTIEPGQQSFVQVRVSPSVSEFLLQLDSCHLDLGPEGGTVELIQGRAAKGNCVSLLSPSPEGDPR
FSFLLHFYTVPIPKTGTLSCTVALRPKTGSQDQEVHRTVFMRLNIISPDLSGCTSKGLVLPAVLGITFGAFLIGALLTAALWYIYSHTRE

--------------------------------------------------------------
>91461_91461_2_TMED4-ENG_TMED4_chr7_44620692_ENST00000457408_ENG_chr9_130581112_ENST00000373203_length(transcript)=1923nt_BP=587nt
GCAGGCGCAGAGCGATGCGCAAATGTGCGCAGGCGCTTAGGGGCTGAGGCGCGATGGCAGGTGTCGGGGCTGGGCCTCTGCGGGCGATGG
GGCGGCAGGCCCTGCTGCTTCTCGCGCTGTGCGCCACAGGCGCCCAGGGGCTCTACTTCCACATCGGCGAGACCGAGAAGCGCTGTTTCA
TCGAGGAAATCCCCGACGAGACCATGGTCATCGGCAACTATCGTACCCAGATGTGGGATAAGCAGAAGGAGGTCTTCCTGCCCTCGACCC
CTGGCCTGGGCATGCACGTGGAAGTGAAGGACCCCGACGGCAAGGTGGTGCTGTCCCGGCAGTACGGCTCGGAGGGCCGCTTCACGTTCA
CCTCCCACACGCCCGGTGACCATCAAATCTGTCTGCACTCCAATTCTACCAGGATGGCTCTCTTCGCTGGTGGCAAACTGCGGGTGCATC
TCGACATCCAGGTTGGGGAGCATGCCAACAACTACCCTGAGATTGCTGCAAAAGATAAGCTGACGGAGCTACAGCTCCGCGCCCGCCAGT
TGCTTGATCAGGTGGAACAGATTCAGAAGGAGCAGGATTACCAAAGGAAAAAGGTGCACTGCCTCAACATGGACAGCCTCTCTTTCCAGC
TGGGCCTCTACCTCAGCCCACACTTCCTCCAGGCCTCCAACACCATCGAGCCGGGGCAGCAGAGCTTTGTGCAGGTCAGAGTGTCCCCAT
CCGTCTCCGAGTTCCTGCTCCAGTTAGACAGCTGCCACCTGGACTTGGGGCCTGAGGGAGGCACCGTGGAACTCATCCAGGGCCGGGCGG
CCAAGGGCAACTGTGTGAGCCTGCTGTCCCCAAGCCCCGAGGGTGACCCGCGCTTCAGCTTCCTCCTCCACTTCTACACAGTACCCATAC
CCAAAACCGGCACCCTCAGCTGCACGGTAGCCCTGCGTCCCAAGACCGGGTCTCAAGACCAGGAAGTCCATAGGACTGTCTTCATGCGCT
TGAACATCATCAGCCCTGACCTGTCTGGTTGCACAAGCAAAGGCCTCGTCCTGCCCGCCGTGCTGGGCATCACCTTTGGTGCCTTCCTCA
TCGGGGCCCTGCTCACTGCTGCACTCTGGTACATCTACTCGCACACGCGTTCCCCCAGCAAGCGGGAGCCCGTGGTGGCGGTGGCTGCCC
CGGCCTCCTCGGAGAGCAGCAGCACCAACCACAGCATCGGGAGCACCCAGAGCACCCCCTGCTCCACCAGCAGCATGGCATAGCCCCGGC
CCCCCGCGCTCGCCCAGCAGGAGAGACTGAGCAGCCGCCAGCTGGGAGCACTGGTGTGAACTCACCCTGGGAGCCAGTCCTCCACTCGAC
CCAGAATGGAGCCTGCTCTCCGCGCCTACCCTTCCCGCCTCCCTCTCAGAGGCCTGCTGCCAGTGCAGCCACTGGCTTGGAACACCTTGG
GGTCCCTCCACCCCACAGAACCTTCAACCCAGTGGGTCTGGGATATGGCTGCCCAGGAGACAGACCACTTGCCACGCTGTTGTAAAAACC
CAAGTCCCTGTCATTTGAACCTGGATCCAGCACTGGTGAACTGAGCTGGGCAGGAAGGGAGAACTTGAAACAGATTCAGGCCAGCCCAGC
CAGGCCAACAGCACCTCCCCGCTGGGAAGAGAAGAGGGCCCAGCCCAGAGCCACCTGGATCTATCCCTGCGGCCTCCACACCTGAACTTG
CCTAACTAACTGGCAGGGGAGACAGGAGCCTAGCGGAGCCCAGCCTGGGAGCCCAGAGGGTGGCAAGAACAGTGGGCGTTGGGAGCCTAG
CTCCTGCCACATGGAGCCCCCTCTGCCGGTCGGGCAGCCAGCAGAGGGGGAGTAGCCAAGCTGCTTGTCCTGGGCCTGCCCCTGTGTATT

>91461_91461_2_TMED4-ENG_TMED4_chr7_44620692_ENST00000457408_ENG_chr9_130581112_ENST00000373203_length(amino acids)=399AA_BP=178
MAGVGAGPLRAMGRQALLLLALCATGAQGLYFHIGETEKRCFIEEIPDETMVIGNYRTQMWDKQKEVFLPSTPGLGMHVEVKDPDGKVVL
SRQYGSEGRFTFTSHTPGDHQICLHSNSTRMALFAGGKLRVHLDIQVGEHANNYPEIAAKDKLTELQLRARQLLDQVEQIQKEQDYQRKK
VHCLNMDSLSFQLGLYLSPHFLQASNTIEPGQQSFVQVRVSPSVSEFLLQLDSCHLDLGPEGGTVELIQGRAAKGNCVSLLSPSPEGDPR
FSFLLHFYTVPIPKTGTLSCTVALRPKTGSQDQEVHRTVFMRLNIISPDLSGCTSKGLVLPAVLGITFGAFLIGALLTAALWYIYSHTRS

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

Top

Fusion Gene PPI Analysis for TMED4-ENG


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 TMED4-ENG


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 TMED4-ENG


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