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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:MED4-HTR2A

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MED4-HTR2A
FusionPDB ID: 52779
FusionGDB2.0 ID: 52779
HgeneTgene
Gene symbol

MED4

HTR2A

Gene ID

29079

3356

Gene namemediator complex subunit 45-hydroxytryptamine receptor 2A
SynonymsARC36|DRIP36|HSPC126|TRAP36|VDRIP5-HT2A|HTR2
Cytomap

13q14.2

13q14.2

Type of geneprotein-codingprotein-coding
Descriptionmediator of RNA polymerase II transcription subunit 4TRAP/SMCC/PC2 subunit p36activator-recruited cofactor 36 kDa componentmediator, 34-kD subunit, homologvitamin D receptor-interacting protein, 36-kDvitamin D3 receptor-interacting protein complex 365-hydroxytryptamine receptor 2A5-HT2 receptor5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupledserotonin 5-HT-2A receptor
Modification date2020031320200315
UniProtAcc

Q9NPJ6

.
Ensembl transtripts involved in fusion geneENST idsENST00000495013, ENST00000258648, 
ENST00000378586, 
ENST00000378688, 
ENST00000542664, ENST00000543956, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 4=1441 X 1 X 1=1
# samples 61
** MAII scorelog2(6/144*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context (manual curation of fusion genes in FusionPDB)

PubMed: MED4 [Title/Abstract] AND HTR2A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MED4(48653980)-HTR2A(47409774), # samples:2
Anticipated loss of major functional domain due to fusion event.MED4-HTR2A 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.
MED4-HTR2A 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.
MED4-HTR2A 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.
MED4-HTR2A 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
HgeneMED4

GO:0006366

transcription by RNA polymerase II

10882111

HgeneMED4

GO:0006367

transcription initiation from RNA polymerase II promoter

12218053

HgeneMED4

GO:0045893

positive regulation of transcription, DNA-templated

10198638

TgeneHTR2A

GO:0006874

cellular calcium ion homeostasis

16517693|19057895

TgeneHTR2A

GO:0007202

activation of phospholipase C activity

16517693

TgeneHTR2A

GO:0010513

positive regulation of phosphatidylinositol biosynthetic process

19057895

TgeneHTR2A

GO:0014065

phosphatidylinositol 3-kinase signaling

16517693

TgeneHTR2A

GO:0042493

response to drug

15862800|18703043

TgeneHTR2A

GO:0051209

release of sequestered calcium ion into cytosol

15862800

TgeneHTR2A

GO:0070374

positive regulation of ERK1 and ERK2 cascade

19057895


check buttonFusion gene breakpoints across MED4 (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 HTR2A (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
ChimerDB4GBMTCGA-12-0619-01AMED4chr13

48653980

-HTR2Achr13

47409774

-


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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)
ENST00000258648MED4chr1348653980-ENST00000378688HTR2Achr1347409774-4756666171468483
ENST00000258648MED4chr1348653980-ENST00000542664HTR2Achr1347409774-2928666171468483
ENST00000258648MED4chr1348653980-ENST00000543956HTR2Achr1347409774-2928666171468483
ENST00000378586MED4chr1348653980-ENST00000378688HTR2Achr1347409774-467758741389461
ENST00000378586MED4chr1348653980-ENST00000542664HTR2Achr1347409774-284958741389461
ENST00000378586MED4chr1348653980-ENST00000543956HTR2Achr1347409774-284958741389461

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
ENST00000258648ENST00000378688MED4chr1348653980-HTR2Achr1347409774-0.000582380.99941766
ENST00000258648ENST00000542664MED4chr1348653980-HTR2Achr1347409774-0.0011480960.9988519
ENST00000258648ENST00000543956MED4chr1348653980-HTR2Achr1347409774-0.0011480960.9988519
ENST00000378586ENST00000378688MED4chr1348653980-HTR2Achr1347409774-0.0003438320.9996562
ENST00000378586ENST00000542664MED4chr1348653980-HTR2Achr1347409774-0.0007937120.99920636
ENST00000378586ENST00000543956MED4chr1348653980-HTR2Achr1347409774-0.0007937120.99920636

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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

>52779_52779_1_MED4-HTR2A_MED4_chr13_48653980_ENST00000258648_HTR2A_chr13_47409774_ENST00000378688_length(amino acids)=483AA_BP=1
MGKMAASSSGEKEKERLGGGLGVAGGNSTRERLLSALEDLEVLSRELIEMLAISRNQKLLQAGEENQVLELLIHRDGEFQELMKLALNQG
KIHHEMQVLEKEVEKRDSDIQQLQKQLKEAEQILATAVYQAKEKLKSIEKARKGAISSEEIIKYAHRISASNAVCAPLTWVPGDPRRPYP
TDLEMRSGLLGQMNNPSTNGVNGHLPGDALAAGRLPGISMPIPVFGLQDDSKVFKEGSCLLADDNFVLIGSFVSFFIPLTIMVITYFLTI
KSLQKEATLCVSDLGTRAKLASFSFLPQSSLSSEKLFQRSIHREPGSYTGRRTMQSISNEQKACKVLGIVFFLFVVMWCPFFITNIMAVI
CKESCNEDVIGALLNVFVWIGYLSSAVNPLVYTLFNKTYRSAFSRYIQCQYKENKKPLQLILVNTIPALAYKSSQLQMGQKKNSKQDAKT

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

>52779_52779_2_MED4-HTR2A_MED4_chr13_48653980_ENST00000258648_HTR2A_chr13_47409774_ENST00000542664_length(amino acids)=483AA_BP=1
MGKMAASSSGEKEKERLGGGLGVAGGNSTRERLLSALEDLEVLSRELIEMLAISRNQKLLQAGEENQVLELLIHRDGEFQELMKLALNQG
KIHHEMQVLEKEVEKRDSDIQQLQKQLKEAEQILATAVYQAKEKLKSIEKARKGAISSEEIIKYAHRISASNAVCAPLTWVPGDPRRPYP
TDLEMRSGLLGQMNNPSTNGVNGHLPGDALAAGRLPGISMPIPVFGLQDDSKVFKEGSCLLADDNFVLIGSFVSFFIPLTIMVITYFLTI
KSLQKEATLCVSDLGTRAKLASFSFLPQSSLSSEKLFQRSIHREPGSYTGRRTMQSISNEQKACKVLGIVFFLFVVMWCPFFITNIMAVI
CKESCNEDVIGALLNVFVWIGYLSSAVNPLVYTLFNKTYRSAFSRYIQCQYKENKKPLQLILVNTIPALAYKSSQLQMGQKKNSKQDAKT

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

>52779_52779_3_MED4-HTR2A_MED4_chr13_48653980_ENST00000258648_HTR2A_chr13_47409774_ENST00000543956_length(amino acids)=483AA_BP=1
MGKMAASSSGEKEKERLGGGLGVAGGNSTRERLLSALEDLEVLSRELIEMLAISRNQKLLQAGEENQVLELLIHRDGEFQELMKLALNQG
KIHHEMQVLEKEVEKRDSDIQQLQKQLKEAEQILATAVYQAKEKLKSIEKARKGAISSEEIIKYAHRISASNAVCAPLTWVPGDPRRPYP
TDLEMRSGLLGQMNNPSTNGVNGHLPGDALAAGRLPGISMPIPVFGLQDDSKVFKEGSCLLADDNFVLIGSFVSFFIPLTIMVITYFLTI
KSLQKEATLCVSDLGTRAKLASFSFLPQSSLSSEKLFQRSIHREPGSYTGRRTMQSISNEQKACKVLGIVFFLFVVMWCPFFITNIMAVI
CKESCNEDVIGALLNVFVWIGYLSSAVNPLVYTLFNKTYRSAFSRYIQCQYKENKKPLQLILVNTIPALAYKSSQLQMGQKKNSKQDAKT

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

>52779_52779_4_MED4-HTR2A_MED4_chr13_48653980_ENST00000378586_HTR2A_chr13_47409774_ENST00000378688_length(amino acids)=461AA_BP=1
MRQLALRVRRWRDSGENGCVFEWELIEMLAISRNQKLLQAGEENQVLELLIHRDGEFQELMKLALNQGKIHHEMQVLEKEVEKRDSDIQQ
LQKQLKEAEQILATAVYQAKEKLKSIEKARKGAISSEEIIKYAHRISASNAVCAPLTWVPGDPRRPYPTDLEMRSGLLGQMNNPSTNGVN
GHLPGDALAAGRLPGISMPIPVFGLQDDSKVFKEGSCLLADDNFVLIGSFVSFFIPLTIMVITYFLTIKSLQKEATLCVSDLGTRAKLAS
FSFLPQSSLSSEKLFQRSIHREPGSYTGRRTMQSISNEQKACKVLGIVFFLFVVMWCPFFITNIMAVICKESCNEDVIGALLNVFVWIGY
LSSAVNPLVYTLFNKTYRSAFSRYIQCQYKENKKPLQLILVNTIPALAYKSSQLQMGQKKNSKQDAKTTDNDCSMVALGKQHSEEASKDN

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

>52779_52779_5_MED4-HTR2A_MED4_chr13_48653980_ENST00000378586_HTR2A_chr13_47409774_ENST00000542664_length(amino acids)=461AA_BP=1
MRQLALRVRRWRDSGENGCVFEWELIEMLAISRNQKLLQAGEENQVLELLIHRDGEFQELMKLALNQGKIHHEMQVLEKEVEKRDSDIQQ
LQKQLKEAEQILATAVYQAKEKLKSIEKARKGAISSEEIIKYAHRISASNAVCAPLTWVPGDPRRPYPTDLEMRSGLLGQMNNPSTNGVN
GHLPGDALAAGRLPGISMPIPVFGLQDDSKVFKEGSCLLADDNFVLIGSFVSFFIPLTIMVITYFLTIKSLQKEATLCVSDLGTRAKLAS
FSFLPQSSLSSEKLFQRSIHREPGSYTGRRTMQSISNEQKACKVLGIVFFLFVVMWCPFFITNIMAVICKESCNEDVIGALLNVFVWIGY
LSSAVNPLVYTLFNKTYRSAFSRYIQCQYKENKKPLQLILVNTIPALAYKSSQLQMGQKKNSKQDAKTTDNDCSMVALGKQHSEEASKDN

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

>52779_52779_6_MED4-HTR2A_MED4_chr13_48653980_ENST00000378586_HTR2A_chr13_47409774_ENST00000543956_length(amino acids)=461AA_BP=1
MRQLALRVRRWRDSGENGCVFEWELIEMLAISRNQKLLQAGEENQVLELLIHRDGEFQELMKLALNQGKIHHEMQVLEKEVEKRDSDIQQ
LQKQLKEAEQILATAVYQAKEKLKSIEKARKGAISSEEIIKYAHRISASNAVCAPLTWVPGDPRRPYPTDLEMRSGLLGQMNNPSTNGVN
GHLPGDALAAGRLPGISMPIPVFGLQDDSKVFKEGSCLLADDNFVLIGSFVSFFIPLTIMVITYFLTIKSLQKEATLCVSDLGTRAKLAS
FSFLPQSSLSSEKLFQRSIHREPGSYTGRRTMQSISNEQKACKVLGIVFFLFVVMWCPFFITNIMAVICKESCNEDVIGALLNVFVWIGY
LSSAVNPLVYTLFNKTYRSAFSRYIQCQYKENKKPLQLILVNTIPALAYKSSQLQMGQKKNSKQDAKTTDNDCSMVALGKQHSEEASKDN

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

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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/chr13:48653980/chr13:47409774)
- 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
MED4

Q9NPJ6

.
FUNCTION: Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors.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
HgeneMED4chr13:48653980chr13:47409774ENST00000258648-6724_48213.33333333333334271.0Coiled coilOntology_term=ECO:0000255
HgeneMED4chr13:48653980chr13:47409774ENST00000258648-6790_131213.33333333333334271.0Coiled coilOntology_term=ECO:0000255
HgeneMED4chr13:48653980chr13:47409774ENST00000378586-6724_48167.33333333333334225.0Coiled coilOntology_term=ECO:0000255
HgeneMED4chr13:48653980chr13:47409774ENST00000378586-6790_131167.33333333333334225.0Coiled coilOntology_term=ECO:0000255
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813376_380204.33333333333334472.0MotifNPxxY motif%3B important for ligand-induced conformation changes and signaling
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813469_471204.33333333333334472.0MotifPDZ-binding
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424376_380204.33333333333334472.0MotifNPxxY motif%3B important for ligand-induced conformation changes and signaling
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424469_471204.33333333333334472.0MotifPDZ-binding
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613172_174120.33333333333333388.0MotifDRY motif%3B important for ligand-induced conformation changes
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613376_380120.33333333333333388.0MotifNPxxY motif%3B important for ligand-induced conformation changes and signaling
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613469_471120.33333333333333388.0MotifPDZ-binding
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813336_340204.33333333333334472.0RegionAgonist binding
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424336_340204.33333333333334472.0RegionAgonist binding
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613155_160120.33333333333333388.0RegionAgonist binding
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613336_340120.33333333333333388.0RegionAgonist binding
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813216_233204.33333333333334472.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813255_324204.33333333333334472.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813347_362204.33333333333334472.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813385_471204.33333333333334472.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424216_233204.33333333333334472.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424255_324204.33333333333334472.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424347_362204.33333333333334472.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424385_471204.33333333333334472.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613133_148120.33333333333333388.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613172_191120.33333333333333388.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613216_233120.33333333333333388.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613255_324120.33333333333333388.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613347_362120.33333333333333388.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613385_471120.33333333333333388.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813234_254204.33333333333334472.0TransmembraneHelical%3B Name%3D5
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813325_346204.33333333333334472.0TransmembraneHelical%3B Name%3D6
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813363_384204.33333333333334472.0TransmembraneHelical%3B Name%3D7
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424234_254204.33333333333334472.0TransmembraneHelical%3B Name%3D5
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424325_346204.33333333333334472.0TransmembraneHelical%3B Name%3D6
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424363_384204.33333333333334472.0TransmembraneHelical%3B Name%3D7
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613149_171120.33333333333333388.0TransmembraneHelical%3B Name%3D3
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613192_215120.33333333333333388.0TransmembraneHelical%3B Name%3D4
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613234_254120.33333333333333388.0TransmembraneHelical%3B Name%3D5
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613325_346120.33333333333333388.0TransmembraneHelical%3B Name%3D6
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613363_384120.33333333333333388.0TransmembraneHelical%3B Name%3D7

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMED4chr13:48653980chr13:47409774ENST00000258648-67262_269213.33333333333334271.0Compositional biasNote=Poly-Ser
HgeneMED4chr13:48653980chr13:47409774ENST00000378586-67262_269167.33333333333334225.0Compositional biasNote=Poly-Ser
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813172_174204.33333333333334472.0MotifDRY motif%3B important for ligand-induced conformation changes
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424172_174204.33333333333334472.0MotifDRY motif%3B important for ligand-induced conformation changes
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813155_160204.33333333333334472.0RegionAgonist binding
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424155_160204.33333333333334472.0RegionAgonist binding
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813100_110204.33333333333334472.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813133_148204.33333333333334472.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813172_191204.33333333333334472.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST00000378688131_75204.33333333333334472.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424100_110204.33333333333334472.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424133_148204.33333333333334472.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424172_191204.33333333333334472.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST00000542664241_75204.33333333333334472.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613100_110120.33333333333333388.0Topological domainCytoplasmic
TgeneHTR2Achr13:48653980chr13:47409774ENST00000543956131_75120.33333333333333388.0Topological domainExtracellular
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813111_132204.33333333333334472.0TransmembraneHelical%3B Name%3D2
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813149_171204.33333333333334472.0TransmembraneHelical%3B Name%3D3
TgeneHTR2Achr13:48653980chr13:47409774ENST0000037868813192_215204.33333333333334472.0TransmembraneHelical%3B Name%3D4
TgeneHTR2Achr13:48653980chr13:47409774ENST000003786881376_99204.33333333333334472.0TransmembraneHelical%3B Name%3D1
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424111_132204.33333333333334472.0TransmembraneHelical%3B Name%3D2
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424149_171204.33333333333334472.0TransmembraneHelical%3B Name%3D3
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054266424192_215204.33333333333334472.0TransmembraneHelical%3B Name%3D4
TgeneHTR2Achr13:48653980chr13:47409774ENST000005426642476_99204.33333333333334472.0TransmembraneHelical%3B Name%3D1
TgeneHTR2Achr13:48653980chr13:47409774ENST0000054395613111_132120.33333333333333388.0TransmembraneHelical%3B Name%3D2
TgeneHTR2Achr13:48653980chr13:47409774ENST000005439561376_99120.33333333333333388.0TransmembraneHelical%3B Name%3D1


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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
MED4
HTR2A


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 MED4-HTR2A


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 MED4-HTR2A


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