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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:CTIF-GRM4

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CTIF-GRM4
FusionPDB ID: 20236
FusionGDB2.0 ID: 20236
HgeneTgene
Gene symbol

CTIF

GRM4

Gene ID

9811

2914

Gene namecap binding complex dependent translation initiation factorglutamate metabotropic receptor 4
SynonymsGm672|KIAA0427GPRC1D|MGLUR4|mGlu4
Cytomap

18q21.1

6p21.31

Type of geneprotein-codingprotein-coding
DescriptionCBP80/20-dependent translation initiation factormetabotropic glutamate receptor 4glutamate receptor, metabotropic 4
Modification date2020031320200313
UniProtAcc

O43310

Main function of 5'-partner protein: FUNCTION: Specifically required for the pioneer round of mRNA translation mediated by the cap-binding complex (CBC), that takes place during or right after mRNA export via the nuclear pore complex (NPC). Acts via its interaction with the NCBP1/CBP80 component of the CBC complex and recruits the 40S small subunit of the ribosome via eIF3. In contrast, it is not involved in steady state translation, that takes place when the CBC complex is replaced by cytoplasmic cap-binding protein eIF4E. Also required for nonsense-mediated mRNA decay (NMD), the pioneer round of mRNA translation mediated by the cap-binding complex playing a central role in nonsense-mediated mRNA decay (NMD). {ECO:0000269|PubMed:19648179}.

Q14833

Main function of 5'-partner protein: FUNCTION: G-protein coupled receptor for glutamate. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors. Signaling inhibits adenylate cyclase activity. {ECO:0000269|PubMed:7617140, ECO:0000269|PubMed:8738157, ECO:0000269|PubMed:9473604}.
Ensembl transtripts involved in fusion geneENST idsENST00000256413, ENST00000382998, 
ENST00000592658, 
ENST00000455714, 
ENST00000535756, ENST00000545715, 
ENST00000609222, ENST00000374177, 
ENST00000374181, ENST00000538487, 
ENST00000544773, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score20 X 11 X 10=22007 X 7 X 6=294
# samples 239
** MAII scorelog2(23/2200*10)=-3.25779775746765
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/294*10)=-1.70781924850669
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CTIF [Title/Abstract] AND GRM4 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CTIF [Title/Abstract] AND GRM4 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CTIF(46197115)-GRM4(34059876), # samples:3
Anticipated loss of major functional domain due to fusion event.CTIF-GRM4 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.
CTIF-GRM4 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.
CTIF-GRM4 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.
CTIF-GRM4 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
TgeneGRM4

GO:0000187

activation of MAPK activity

15102938



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/chr18:46197115/chr6:34059876)
- 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 buttonRetention analysis results 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, are available here.

check buttonFusion gene breakpoints across CTIF (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 GRM4 (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 Amino Acid Sequences


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)
ENST00000256413CTIFchr1846197115+ENST00000538487GRM4chr634059876-39928022953021908
ENST00000256413CTIFchr1846197115+ENST00000374181GRM4chr634059876-39918022953021908
ENST00000256413CTIFchr1846197115+ENST00000374177GRM4chr634059876-38488022952880861
ENST00000256413CTIFchr1846197115+ENST00000544773GRM4chr634059876-34108022953021908
ENST00000382998CTIFchr1846197115+ENST00000538487GRM4chr634059876-39547642572983908
ENST00000382998CTIFchr1846197115+ENST00000374181GRM4chr634059876-39537642572983908
ENST00000382998CTIFchr1846197115+ENST00000374177GRM4chr634059876-38107642572842861
ENST00000382998CTIFchr1846197115+ENST00000544773GRM4chr634059876-33727642572983908

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
ENST00000256413ENST00000538487CTIFchr1846197115+GRM4chr634059876-0.0027335520.9972664
ENST00000256413ENST00000374181CTIFchr1846197115+GRM4chr634059876-0.0027184650.99728155
ENST00000256413ENST00000374177CTIFchr1846197115+GRM4chr634059876-0.0031260430.996874
ENST00000256413ENST00000544773CTIFchr1846197115+GRM4chr634059876-0.003910490.9960896
ENST00000382998ENST00000538487CTIFchr1846197115+GRM4chr634059876-0.0033904950.99660957
ENST00000382998ENST00000374181CTIFchr1846197115+GRM4chr634059876-0.0033678180.99663216
ENST00000382998ENST00000374177CTIFchr1846197115+GRM4chr634059876-0.0038208860.9961791
ENST00000382998ENST00000544773CTIFchr1846197115+GRM4chr634059876-0.0051072360.9948927

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for CTIF-GRM4

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CTIFchr1846197115GRM4chr634059876764166DGINLNDIEKVLPAWQIPQISYASTA
CTIFchr1846197115GRM4chr634059876802166DGINLNDIEKVLPAWQIPQISYASTA

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Potential FusionNeoAntigen Information of CTIF-GRM4 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
CTIF-GRM4_46197115_34059876.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
CTIF-GRM4chr1846197115chr634059876802HLA-B44:03IEKVLPAW0.99880.932715
CTIF-GRM4chr1846197115chr634059876802HLA-B18:01IEKVLPAW0.99090.8104715
CTIF-GRM4chr1846197115chr634059876802HLA-B51:01LPAWQIPQI0.99620.81461120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:02LPAWQIPQI0.99160.8221120
CTIF-GRM4chr1846197115chr634059876802HLA-B56:01LPAWQIPQI0.98060.72171120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:03LPAWQIPQI0.97320.81031120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:02LPAWQIPQI0.96920.96191120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:04LPAWQIPQI0.96920.96191120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:05LPAWQIPQI0.93990.68471120
CTIF-GRM4chr1846197115chr634059876802HLA-B53:01LPAWQIPQI0.93640.65431120
CTIF-GRM4chr1846197115chr634059876802HLA-B07:05LPAWQIPQI0.89370.5441120
CTIF-GRM4chr1846197115chr634059876802HLA-B53:01DIEKVLPAW0.88210.5898615
CTIF-GRM4chr1846197115chr634059876802HLA-B55:01LPAWQIPQI0.82940.58981120
CTIF-GRM4chr1846197115chr634059876802HLA-B82:01LPAWQIPQI0.33320.94181120
CTIF-GRM4chr1846197115chr634059876802HLA-B81:01LPAWQIPQI0.28910.92241120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:01LPAWQIPQISY0.99170.84211122
CTIF-GRM4chr1846197115chr634059876802HLA-B35:08LPAWQIPQISY0.98740.83511122
CTIF-GRM4chr1846197115chr634059876802HLA-B35:05LPAWQIPQISY0.94020.55411122
CTIF-GRM4chr1846197115chr634059876802HLA-B53:01LPAWQIPQISY0.88370.54631122
CTIF-GRM4chr1846197115chr634059876802HLA-B78:01LPAWQIPQI0.99620.82661120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:07LPAWQIPQI0.99520.9811120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:12LPAWQIPQI0.96920.96191120
CTIF-GRM4chr1846197115chr634059876802HLA-B54:01LPAWQIPQI0.96470.89531120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:08LPAWQIPQI0.95840.74831120
CTIF-GRM4chr1846197115chr634059876802HLA-B56:04LPAWQIPQI0.88370.90351120
CTIF-GRM4chr1846197115chr634059876802HLA-B07:12LPAWQIPQI0.77570.52951120
CTIF-GRM4chr1846197115chr634059876802HLA-B07:04LPAWQIPQI0.64490.51761120
CTIF-GRM4chr1846197115chr634059876802HLA-B42:02LPAWQIPQI0.56450.92381120
CTIF-GRM4chr1846197115chr634059876802HLA-B42:01LPAWQIPQI0.52250.91921120
CTIF-GRM4chr1846197115chr634059876802HLA-B39:10LPAWQIPQI0.35210.98341120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:07EKVLPAWQI0.08180.8825817
CTIF-GRM4chr1846197115chr634059876802HLA-A02:07VLPAWQIPQI0.94210.53271020
CTIF-GRM4chr1846197115chr634059876802HLA-B15:31LPAWQIPQISY0.99020.82721122
CTIF-GRM4chr1846197115chr634059876802HLA-B44:13IEKVLPAW0.99880.932715
CTIF-GRM4chr1846197115chr634059876802HLA-B44:07IEKVLPAW0.99880.932715
CTIF-GRM4chr1846197115chr634059876802HLA-B44:26IEKVLPAW0.99880.932715
CTIF-GRM4chr1846197115chr634059876802HLA-B18:05IEKVLPAW0.99090.8104715
CTIF-GRM4chr1846197115chr634059876802HLA-B18:03IEKVLPAW0.98840.7935715
CTIF-GRM4chr1846197115chr634059876802HLA-B51:13PAWQIPQI0.97610.58191220
CTIF-GRM4chr1846197115chr634059876802HLA-B78:02LPAWQIPQI0.99670.83951120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:13LPAWQIPQI0.99610.7471120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:14LPAWQIPQI0.9960.81071120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:22LPAWQIPQI0.99510.84471120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:09LPAWQIPQI0.99470.78871120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:06LPAWQIPQI0.99270.78911120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:21LPAWQIPQI0.99170.82491120
CTIF-GRM4chr1846197115chr634059876802HLA-B56:05LPAWQIPQI0.98720.78781120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:13LPAWQIPQI0.97410.82551120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:09LPAWQIPQI0.96920.96191120
CTIF-GRM4chr1846197115chr634059876802HLA-B53:02DIEKVLPAW0.96720.7592615
CTIF-GRM4chr1846197115chr634059876802HLA-B35:17LPAWQIPQI0.93520.77391120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:30LPAWQIPQI0.93520.77391120
CTIF-GRM4chr1846197115chr634059876802HLA-B55:02LPAWQIPQI0.93140.78611120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:29LPAWQIPQI0.93010.72611120
CTIF-GRM4chr1846197115chr634059876802HLA-B59:01LPAWQIPQI0.92970.82311120
CTIF-GRM4chr1846197115chr634059876802HLA-B51:05LPAWQIPQI0.9180.611120
CTIF-GRM4chr1846197115chr634059876802HLA-B53:02LPAWQIPQI0.90660.62151120
CTIF-GRM4chr1846197115chr634059876802HLA-B56:02LPAWQIPQI0.88370.90351120
CTIF-GRM4chr1846197115chr634059876802HLA-B55:04LPAWQIPQI0.87990.9231120
CTIF-GRM4chr1846197115chr634059876802HLA-A25:01DIEKVLPAW0.76260.923615
CTIF-GRM4chr1846197115chr634059876802HLA-B15:13DIEKVLPAW0.67450.8837615
CTIF-GRM4chr1846197115chr634059876802HLA-B07:26LPAWQIPQI0.65460.52231120
CTIF-GRM4chr1846197115chr634059876802HLA-B67:01LPAWQIPQI0.50570.98111120
CTIF-GRM4chr1846197115chr634059876802HLA-B82:02LPAWQIPQI0.33320.94181120
CTIF-GRM4chr1846197115chr634059876802HLA-B35:77LPAWQIPQISY0.99170.84211122
CTIF-GRM4chr1846197115chr634059876802HLA-B35:23LPAWQIPQISY0.99170.8891122
CTIF-GRM4chr1846197115chr634059876802HLA-B35:20LPAWQIPQISY0.9910.89991122
CTIF-GRM4chr1846197115chr634059876802HLA-B35:24LPAWQIPQISY0.98630.81751122
CTIF-GRM4chr1846197115chr634059876802HLA-B35:30LPAWQIPQISY0.95940.74351122
CTIF-GRM4chr1846197115chr634059876802HLA-B35:17LPAWQIPQISY0.95940.74351122
CTIF-GRM4chr1846197115chr634059876802HLA-B35:11LPAWQIPQISY0.94410.86951122
CTIF-GRM4chr1846197115chr634059876802HLA-B15:08LPAWQIPQISY0.90230.77921122
CTIF-GRM4chr1846197115chr634059876802HLA-B15:11LPAWQIPQISY0.89820.78921122
CTIF-GRM4chr1846197115chr634059876802HLA-B35:43LPAWQIPQISY0.89590.78481122
CTIF-GRM4chr1846197115chr634059876802HLA-B53:02LPAWQIPQISY0.84910.52091122

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Potential FusionNeoAntigen Information of CTIF-GRM4 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
CTIF-GRM4_46197115_34059876.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)
CTIF-GRM4chr1846197115chr634059876802DRB3-0301DGINLNDIEKVLPAW015

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Fusion breakpoint peptide structures of CTIF-GRM4

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
1145DIEKVLPAWQIPQICTIFGRM4chr1846197115chr634059876802

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CTIF-GRM4

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN1145DIEKVLPAWQIPQI-7.15543-7.26883
HLA-B14:023BVN1145DIEKVLPAWQIPQI-4.77435-5.80965
HLA-B52:013W391145DIEKVLPAWQIPQI-6.80875-6.92215
HLA-B52:013W391145DIEKVLPAWQIPQI-4.20386-5.23916
HLA-A11:014UQ21145DIEKVLPAWQIPQI-7.5194-8.5547
HLA-A11:014UQ21145DIEKVLPAWQIPQI-6.9601-7.0735
HLA-A24:025HGA1145DIEKVLPAWQIPQI-7.52403-7.63743
HLA-A24:025HGA1145DIEKVLPAWQIPQI-5.82433-6.85963
HLA-B27:056PYJ1145DIEKVLPAWQIPQI-3.28285-4.31815
HLA-B44:053DX81145DIEKVLPAWQIPQI-5.91172-6.94702
HLA-B44:053DX81145DIEKVLPAWQIPQI-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of CTIF-GRM4

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
CTIF-GRM4chr1846197115chr6340598761020VLPAWQIPQIGCCTGGCAGATACCCCAGATCAGCTACGCC
CTIF-GRM4chr1846197115chr6340598761120LPAWQIPQITGGCAGATACCCCAGATCAGCTACGCC
CTIF-GRM4chr1846197115chr6340598761122LPAWQIPQISYTGGCAGATACCCCAGATCAGCTACGCCTCCACA
CTIF-GRM4chr1846197115chr6340598761220PAWQIPQICAGATACCCCAGATCAGCTACGCC
CTIF-GRM4chr1846197115chr634059876615DIEKVLPAWAAGGTCCTTCCAGCCTGGCAGATACCC
CTIF-GRM4chr1846197115chr634059876715IEKVLPAWGTCCTTCCAGCCTGGCAGATACCC
CTIF-GRM4chr1846197115chr634059876817EKVLPAWQICTTCCAGCCTGGCAGATACCCCAGATC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CTIF-GRM4chr1846197115chr634059876015DGINLNDIEKVLPAWAACCTGAATGACATCGAGAAGGTCCTTCCAGCCTGGCAGATACCC

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Information of the samples that have these potential fusion neoantigens of CTIF-GRM4

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
KIRCCTIF-GRM4chr1846197115ENST00000256413chr634059876ENST00000374177TCGA-B0-4945-01A

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Potential target of CAR-T therapy development for CTIF-GRM4

check button Predicted 3D structure. We used RoseTTAFold.

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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneGRM4chr18:46197115chr6:34059876ENST0000037417709588_6100797.0TransmembraneHelical%3B Name%3D1
TgeneGRM4chr18:46197115chr6:34059876ENST0000037417709625_6450797.0TransmembraneHelical%3B Name%3D2
TgeneGRM4chr18:46197115chr6:34059876ENST0000037417709657_6750797.0TransmembraneHelical%3B Name%3D3
TgeneGRM4chr18:46197115chr6:34059876ENST0000037417709700_7200797.0TransmembraneHelical%3B Name%3D4
TgeneGRM4chr18:46197115chr6:34059876ENST0000037417709751_7720797.0TransmembraneHelical%3B Name%3D5
TgeneGRM4chr18:46197115chr6:34059876ENST0000037417709786_8080797.0TransmembraneHelical%3B Name%3D6
TgeneGRM4chr18:46197115chr6:34059876ENST0000037417709822_8470797.0TransmembraneHelical%3B Name%3D7
TgeneGRM4chr18:46197115chr6:34059876ENST00000374181010588_6100913.0TransmembraneHelical%3B Name%3D1
TgeneGRM4chr18:46197115chr6:34059876ENST00000374181010625_6450913.0TransmembraneHelical%3B Name%3D2
TgeneGRM4chr18:46197115chr6:34059876ENST00000374181010657_6750913.0TransmembraneHelical%3B Name%3D3
TgeneGRM4chr18:46197115chr6:34059876ENST00000374181010700_7200913.0TransmembraneHelical%3B Name%3D4
TgeneGRM4chr18:46197115chr6:34059876ENST00000374181010751_7720913.0TransmembraneHelical%3B Name%3D5
TgeneGRM4chr18:46197115chr6:34059876ENST00000374181010786_8080913.0TransmembraneHelical%3B Name%3D6
TgeneGRM4chr18:46197115chr6:34059876ENST00000374181010822_8470913.0TransmembraneHelical%3B Name%3D7
TgeneGRM4chr18:46197115chr6:34059876ENST00000455714010588_6100773.0TransmembraneHelical%3B Name%3D1
TgeneGRM4chr18:46197115chr6:34059876ENST00000455714010625_6450773.0TransmembraneHelical%3B Name%3D2
TgeneGRM4chr18:46197115chr6:34059876ENST00000455714010657_6750773.0TransmembraneHelical%3B Name%3D3
TgeneGRM4chr18:46197115chr6:34059876ENST00000455714010700_7200773.0TransmembraneHelical%3B Name%3D4
TgeneGRM4chr18:46197115chr6:34059876ENST00000455714010751_7720773.0TransmembraneHelical%3B Name%3D5
TgeneGRM4chr18:46197115chr6:34059876ENST00000455714010786_8080773.0TransmembraneHelical%3B Name%3D6
TgeneGRM4chr18:46197115chr6:34059876ENST00000455714010822_8470773.0TransmembraneHelical%3B Name%3D7
TgeneGRM4chr18:46197115chr6:34059876ENST00000535756010588_6100780.0TransmembraneHelical%3B Name%3D1
TgeneGRM4chr18:46197115chr6:34059876ENST00000535756010625_6450780.0TransmembraneHelical%3B Name%3D2
TgeneGRM4chr18:46197115chr6:34059876ENST00000535756010657_6750780.0TransmembraneHelical%3B Name%3D3
TgeneGRM4chr18:46197115chr6:34059876ENST00000535756010700_7200780.0TransmembraneHelical%3B Name%3D4
TgeneGRM4chr18:46197115chr6:34059876ENST00000535756010751_7720780.0TransmembraneHelical%3B Name%3D5
TgeneGRM4chr18:46197115chr6:34059876ENST00000535756010786_8080780.0TransmembraneHelical%3B Name%3D6
TgeneGRM4chr18:46197115chr6:34059876ENST00000535756010822_8470780.0TransmembraneHelical%3B Name%3D7
TgeneGRM4chr18:46197115chr6:34059876ENST00000538487111588_6100913.0TransmembraneHelical%3B Name%3D1
TgeneGRM4chr18:46197115chr6:34059876ENST00000538487111625_6450913.0TransmembraneHelical%3B Name%3D2
TgeneGRM4chr18:46197115chr6:34059876ENST00000538487111657_6750913.0TransmembraneHelical%3B Name%3D3
TgeneGRM4chr18:46197115chr6:34059876ENST00000538487111700_7200913.0TransmembraneHelical%3B Name%3D4
TgeneGRM4chr18:46197115chr6:34059876ENST00000538487111751_7720913.0TransmembraneHelical%3B Name%3D5
TgeneGRM4chr18:46197115chr6:34059876ENST00000538487111786_8080913.0TransmembraneHelical%3B Name%3D6
TgeneGRM4chr18:46197115chr6:34059876ENST00000538487111822_8470913.0TransmembraneHelical%3B Name%3D7
TgeneGRM4chr18:46197115chr6:34059876ENST00000544773010588_6100744.0TransmembraneHelical%3B Name%3D1
TgeneGRM4chr18:46197115chr6:34059876ENST00000544773010625_6450744.0TransmembraneHelical%3B Name%3D2
TgeneGRM4chr18:46197115chr6:34059876ENST00000544773010657_6750744.0TransmembraneHelical%3B Name%3D3
TgeneGRM4chr18:46197115chr6:34059876ENST00000544773010700_7200744.0TransmembraneHelical%3B Name%3D4
TgeneGRM4chr18:46197115chr6:34059876ENST00000544773010751_7720744.0TransmembraneHelical%3B Name%3D5
TgeneGRM4chr18:46197115chr6:34059876ENST00000544773010786_8080744.0TransmembraneHelical%3B Name%3D6
TgeneGRM4chr18:46197115chr6:34059876ENST00000544773010822_8470744.0TransmembraneHelical%3B Name%3D7

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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Related Drugs to CTIF-GRM4

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 CTIF-GRM4

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