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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:PCCA-GRM3

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PCCA-GRM3
FusionPDB ID: 63154
FusionGDB2.0 ID: 63154
HgeneTgene
Gene symbol

PCCA

GRM3

Gene ID

5095

2913

Gene namepropionyl-CoA carboxylase subunit alphaglutamate metabotropic receptor 3
Synonyms-GLUR3|GPRC1C|MGLUR3|mGlu3
Cytomap

13q32.3

7q21.11-q21.12

Type of geneprotein-codingprotein-coding
Descriptionpropionyl-CoA carboxylase alpha chain, mitochondrialPCCase alpha subunitpccA complementation grouppropanoyl-CoA:carbon dioxide ligase alpha subunitpropionyl CoA carboxylase, alpha polypeptidepropionyl Coenzyme A carboxylase, alpha polypeptidepropionmetabotropic glutamate receptor 3glutamate receptor, metabotropic 3
Modification date2020031320200313
UniProtAcc.

Q14832

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:8840013}.
Ensembl transtripts involved in fusion geneENST idsENST00000376285, ENST00000376286, 
ENST00000376279, ENST00000485946, 
ENST00000394720, ENST00000439827, 
ENST00000536043, ENST00000546348, 
ENST00000361669, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score20 X 16 X 12=38406 X 6 X 3=108
# samples 256
** MAII scorelog2(25/3840*10)=-3.94110631094643
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PCCA [Title/Abstract] AND GRM3 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PCCA [Title/Abstract] AND GRM3 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PCCA(101167821)-GRM3(86415576), # samples:1
Anticipated loss of major functional domain due to fusion event.PCCA-GRM3 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.
PCCA-GRM3 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.
PCCA-GRM3 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.
PCCA-GRM3 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


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/chr13:101167821/chr7:86415576)
- 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 PCCA (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 GRM3 (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)
ENST00000376286PCCAchr13101167821+ENST00000361669GRM3chr786415576+476920686442391391
ENST00000376285PCCAchr13101167821+ENST00000361669GRM3chr786415576+477920783842491403

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
ENST00000376286ENST00000361669PCCAchr13101167821+GRM3chr786415576+0.0004606480.9995394
ENST00000376285ENST00000361669PCCAchr13101167821+GRM3chr786415576+0.0003511250.9996489

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 PCCA-GRM3

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PCCAchr13101167821GRM3chr7864155762068668GVVVAVSVKPGDAVANLLRLFQIPQI
PCCAchr13101167821GRM3chr7864155762078680GVVVAVSVKPGDAVANLLRLFQIPQI

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Potential FusionNeoAntigen Information of PCCA-GRM3 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.
PCCA-GRM3_101167821_86415576.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)
PCCA-GRM3chr13101167821chr7864155762078HLA-A26:02DAVANLLRL0.99880.53721120
PCCA-GRM3chr13101167821chr7864155762078HLA-B07:05KPGDAVANL0.99870.5291817
PCCA-GRM3chr13101167821chr7864155762078HLA-B07:02KPGDAVANL0.99870.6217817
PCCA-GRM3chr13101167821chr7864155762078HLA-B15:17AVANLLRLF0.99690.90361221
PCCA-GRM3chr13101167821chr7864155762078HLA-B15:16AVANLLRLF0.99480.90321221
PCCA-GRM3chr13101167821chr7864155762078HLA-A31:08AVANLLRLF0.99350.51051221
PCCA-GRM3chr13101167821chr7864155762078HLA-B58:02AVANLLRLF0.98670.94891221
PCCA-GRM3chr13101167821chr7864155762078HLA-B57:03AVANLLRLF0.98320.99071221
PCCA-GRM3chr13101167821chr7864155762078HLA-A32:13AVANLLRLF0.97760.94391221
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:03DAVANLLRL0.97360.86391120
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:02DAVANLLRL0.83240.94731120
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:04DAVANLLRL0.83240.94731120
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:03KPGDAVANL0.80720.9143817
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:04KPGDAVANL0.51690.9804817
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:02KPGDAVANL0.51690.9804817
PCCA-GRM3chr13101167821chr7864155762078HLA-B81:01KPGDAVANL0.0580.6862817
PCCA-GRM3chr13101167821chr7864155762078HLA-B82:01KPGDAVANL0.01190.6045817
PCCA-GRM3chr13101167821chr7864155762078HLA-A26:15DAVANLLRLF0.99540.61791121
PCCA-GRM3chr13101167821chr7864155762078HLA-A26:14DAVANLLRLF0.99540.61791121
PCCA-GRM3chr13101167821chr7864155762078HLA-B51:07DAVANLLRL0.98650.73021120
PCCA-GRM3chr13101167821chr7864155762078HLA-B78:01DAVANLLRL0.98150.61761120
PCCA-GRM3chr13101167821chr7864155762078HLA-C15:04AVANLLRLF0.97460.93241221
PCCA-GRM3chr13101167821chr7864155762078HLA-B07:12KPGDAVANL0.96920.7467817
PCCA-GRM3chr13101167821chr7864155762078HLA-C03:14AVANLLRLF0.86690.98171221
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:12DAVANLLRL0.83240.94731120
PCCA-GRM3chr13101167821chr7864155762078HLA-C12:12AVANLLRLF0.83110.95711221
PCCA-GRM3chr13101167821chr7864155762078HLA-B07:04KPGDAVANL0.76820.5652817
PCCA-GRM3chr13101167821chr7864155762078HLA-B56:04KPGDAVANL0.72610.765817
PCCA-GRM3chr13101167821chr7864155762078HLA-C12:04AVANLLRLF0.62860.99281221
PCCA-GRM3chr13101167821chr7864155762078HLA-C06:03AVANLLRLF0.61630.99371221
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:12KPGDAVANL0.51690.9804817
PCCA-GRM3chr13101167821chr7864155762078HLA-B39:10KPGDAVANL0.50130.9574817
PCCA-GRM3chr13101167821chr7864155762078HLA-B42:02KPGDAVANL0.11340.7144817
PCCA-GRM3chr13101167821chr7864155762078HLA-B42:01KPGDAVANL0.10950.7077817
PCCA-GRM3chr13101167821chr7864155762078HLA-A26:01DAVANLLRLF0.99540.61791121
PCCA-GRM3chr13101167821chr7864155762078HLA-B07:12KPGDAVANLL0.98210.5613818
PCCA-GRM3chr13101167821chr7864155762078HLA-A25:01DAVANLLRL0.99870.89661120
PCCA-GRM3chr13101167821chr7864155762078HLA-B07:22KPGDAVANL0.99870.6217817
PCCA-GRM3chr13101167821chr7864155762078HLA-B07:09KPGDAVANL0.99850.6238817
PCCA-GRM3chr13101167821chr7864155762078HLA-B57:04AVANLLRLF0.99760.80841221
PCCA-GRM3chr13101167821chr7864155762078HLA-B58:06AVANLLRLF0.99540.89941221
PCCA-GRM3chr13101167821chr7864155762078HLA-A32:01AVANLLRLF0.9940.96681221
PCCA-GRM3chr13101167821chr7864155762078HLA-B57:02AVANLLRLF0.99130.95141221
PCCA-GRM3chr13101167821chr7864155762078HLA-B78:02DAVANLLRL0.98620.68861120
PCCA-GRM3chr13101167821chr7864155762078HLA-B15:24AVANLLRLF0.98490.92551221
PCCA-GRM3chr13101167821chr7864155762078HLA-C15:09AVANLLRLF0.97460.93241221
PCCA-GRM3chr13101167821chr7864155762078HLA-A69:01DAVANLLRL0.94530.61561120
PCCA-GRM3chr13101167821chr7864155762078HLA-A25:01AVANLLRLF0.93310.93411221
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:09DAVANLLRL0.83240.94731120
PCCA-GRM3chr13101167821chr7864155762078HLA-C03:06VSVKPGDAV0.81780.9826514
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:13KPGDAVANL0.74950.9153817
PCCA-GRM3chr13101167821chr7864155762078HLA-B56:02KPGDAVANL0.72610.765817
PCCA-GRM3chr13101167821chr7864155762078HLA-C16:02AVANLLRLF0.71440.98981221
PCCA-GRM3chr13101167821chr7864155762078HLA-B55:04KPGDAVANL0.65440.8183817
PCCA-GRM3chr13101167821chr7864155762078HLA-B59:01KPGDAVANL0.590.7032817
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:22KPGDAVANL0.58720.8266817
PCCA-GRM3chr13101167821chr7864155762078HLA-B67:01KPGDAVANL0.53570.9559817
PCCA-GRM3chr13101167821chr7864155762078HLA-C02:02AVANLLRLF0.52090.9731221
PCCA-GRM3chr13101167821chr7864155762078HLA-C02:10AVANLLRLF0.52090.9731221
PCCA-GRM3chr13101167821chr7864155762078HLA-B35:09KPGDAVANL0.51690.9804817
PCCA-GRM3chr13101167821chr7864155762078HLA-B51:05KPGDAVANL0.38220.5919817
PCCA-GRM3chr13101167821chr7864155762078HLA-B07:26KPGDAVANL0.35540.5546817
PCCA-GRM3chr13101167821chr7864155762078HLA-B82:02KPGDAVANL0.01190.6045817
PCCA-GRM3chr13101167821chr7864155762078HLA-A25:01DAVANLLRLF0.99730.90341121
PCCA-GRM3chr13101167821chr7864155762078HLA-B67:01KPGDAVANLL0.43130.9183818

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Potential FusionNeoAntigen Information of PCCA-GRM3 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.
PCCA-GRM3_101167821_86415576.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)
PCCA-GRM3chr13101167821chr7864155762078DRB1-0806GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-0810GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-0812GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-0822GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-0829GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-0840GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1303GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-13101GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1310GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1312GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1313GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1332GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1348GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1349GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1355GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1358GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1366GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1381GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1388GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1389GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1390GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1394GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1395GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1470GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1473GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1474GVVVAVSVKPGDAVA015
PCCA-GRM3chr13101167821chr7864155762078DRB1-1478GVVVAVSVKPGDAVA015

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Fusion breakpoint peptide structures of PCCA-GRM3

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
9153SVKPGDAVANLLRLPCCAGRM3chr13101167821chr7864155762078

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PCCA-GRM3

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-B14:023BVN9153SVKPGDAVANLLRL-7.15543-7.26883
HLA-B14:023BVN9153SVKPGDAVANLLRL-4.77435-5.80965
HLA-B52:013W399153SVKPGDAVANLLRL-6.80875-6.92215
HLA-B52:013W399153SVKPGDAVANLLRL-4.20386-5.23916
HLA-A11:014UQ29153SVKPGDAVANLLRL-7.5194-8.5547
HLA-A11:014UQ29153SVKPGDAVANLLRL-6.9601-7.0735
HLA-A24:025HGA9153SVKPGDAVANLLRL-7.52403-7.63743
HLA-A24:025HGA9153SVKPGDAVANLLRL-5.82433-6.85963
HLA-B27:056PYJ9153SVKPGDAVANLLRL-3.28285-4.31815
HLA-B44:053DX89153SVKPGDAVANLLRL-5.91172-6.94702
HLA-B44:053DX89153SVKPGDAVANLLRL-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of PCCA-GRM3

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
PCCA-GRM3chr13101167821chr7864155761120DAVANLLRLGACGCGGTGGCAAACCTGCTGCGGCTC
PCCA-GRM3chr13101167821chr7864155761121DAVANLLRLFGACGCGGTGGCAAACCTGCTGCGGCTCTTC
PCCA-GRM3chr13101167821chr7864155761221AVANLLRLFGCGGTGGCAAACCTGCTGCGGCTCTTC
PCCA-GRM3chr13101167821chr786415576514VSVKPGDAVGTCTCTGTCAAGCCTGGAGACGCGGTG
PCCA-GRM3chr13101167821chr786415576817KPGDAVANLAAGCCTGGAGACGCGGTGGCAAACCTG
PCCA-GRM3chr13101167821chr786415576818KPGDAVANLLAAGCCTGGAGACGCGGTGGCAAACCTGCTG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PCCA-GRM3chr13101167821chr786415576015GVVVAVSVKPGDAVAGGAGTGGTGGTGGCCGTCTCTGTCAAGCCTGGAGACGCGGTGGCA

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Information of the samples that have these potential fusion neoantigens of PCCA-GRM3

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
SARCPCCA-GRM3chr13101167821ENST00000376285chr786415576ENST00000361669TCGA-SI-A71O

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Potential target of CAR-T therapy development for PCCA-GRM3

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
TgeneGRM3chr13:101167821chr7:86415576ENST0000036166916577_5990880.0TransmembraneHelical%3B Name%3D1
TgeneGRM3chr13:101167821chr7:86415576ENST0000036166916614_6340880.0TransmembraneHelical%3B Name%3D2
TgeneGRM3chr13:101167821chr7:86415576ENST0000036166916646_6640880.0TransmembraneHelical%3B Name%3D3
TgeneGRM3chr13:101167821chr7:86415576ENST0000036166916689_7090880.0TransmembraneHelical%3B Name%3D4
TgeneGRM3chr13:101167821chr7:86415576ENST0000036166916735_7560880.0TransmembraneHelical%3B Name%3D5
TgeneGRM3chr13:101167821chr7:86415576ENST0000036166916770_7920880.0TransmembraneHelical%3B Name%3D6
TgeneGRM3chr13:101167821chr7:86415576ENST0000036166916803_8280880.0TransmembraneHelical%3B Name%3D7
TgeneGRM3chr13:101167821chr7:86415576ENST0000039472015577_5990536.0TransmembraneHelical%3B Name%3D1
TgeneGRM3chr13:101167821chr7:86415576ENST0000039472015614_6340536.0TransmembraneHelical%3B Name%3D2
TgeneGRM3chr13:101167821chr7:86415576ENST0000039472015646_6640536.0TransmembraneHelical%3B Name%3D3
TgeneGRM3chr13:101167821chr7:86415576ENST0000039472015689_7090536.0TransmembraneHelical%3B Name%3D4
TgeneGRM3chr13:101167821chr7:86415576ENST0000039472015735_7560536.0TransmembraneHelical%3B Name%3D5
TgeneGRM3chr13:101167821chr7:86415576ENST0000039472015770_7920536.0TransmembraneHelical%3B Name%3D6
TgeneGRM3chr13:101167821chr7:86415576ENST0000039472015803_8280536.0TransmembraneHelical%3B Name%3D7
TgeneGRM3chr13:101167821chr7:86415576ENST0000043982715577_5990538.0TransmembraneHelical%3B Name%3D1
TgeneGRM3chr13:101167821chr7:86415576ENST0000043982715614_6340538.0TransmembraneHelical%3B Name%3D2
TgeneGRM3chr13:101167821chr7:86415576ENST0000043982715646_6640538.0TransmembraneHelical%3B Name%3D3
TgeneGRM3chr13:101167821chr7:86415576ENST0000043982715689_7090538.0TransmembraneHelical%3B Name%3D4
TgeneGRM3chr13:101167821chr7:86415576ENST0000043982715735_7560538.0TransmembraneHelical%3B Name%3D5
TgeneGRM3chr13:101167821chr7:86415576ENST0000043982715770_7920538.0TransmembraneHelical%3B Name%3D6
TgeneGRM3chr13:101167821chr7:86415576ENST0000043982715803_8280538.0TransmembraneHelical%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 PCCA-GRM3

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 PCCA-GRM3

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