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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:TPM4-GPR37L1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TPM4-GPR37L1
FusionPDB ID: 93402
FusionGDB2.0 ID: 93402
HgeneTgene
Gene symbol

TPM4

GPR37L1

Gene ID

7171

9283

Gene nametropomyosin 4G protein-coupled receptor 37 like 1
SynonymsHEL-S-108ET(B)R-LP-2|ETBR-LP-2|ETBRLP2
Cytomap

19p13.12-p13.11

1q32.1

Type of geneprotein-codingprotein-coding
Descriptiontropomyosin alpha-4 chainTM30p1epididymis secretory protein Li 108G-protein coupled receptor 37-like 1endothelin B receptor-like protein 2endothelin type b receptor-like protein 2prosaposin receptor GPR37L1
Modification date2020032020200313
UniProtAcc

P67936

Main function of 5'-partner protein: FUNCTION: Binds to actin filaments in muscle and non-muscle cells. Plays a central role, in association with the troponin complex, in the calcium dependent regulation of vertebrate striated muscle contraction. Smooth muscle contraction is regulated by interaction with caldesmon. In non-muscle cells is implicated in stabilizing cytoskeleton actin filaments (By similarity). Binds calcium (PubMed:1836432). {ECO:0000250|UniProtKB:P09495, ECO:0000269|PubMed:1836432}.

O60883

Main function of 5'-partner protein: FUNCTION: G-protein coupled receptor (PubMed:27072655). Has been shown to bind the neuroprotective and glioprotective factor prosaposin (PSAP), leading to endocytosis followed by an ERK phosphorylation cascade (PubMed:23690594). However, other studies have shown that prosaposin does not increase activity (PubMed:27072655, PubMed:28688853). It has been suggested that GPR37L1 is a constitutively active receptor which signals through the guanine nucleotide-binding protein G(s) subunit alpha (PubMed:27072655). Participates in the regulation of postnatal cerebellar development by modulating the Shh pathway (By similarity). Regulates baseline blood pressure in females and protects against cardiovascular stress in males (By similarity). Mediates inhibition of astrocyte glutamate transporters and reduction in neuronal N-methyl-D-aspartate receptor activity (By similarity). {ECO:0000250|UniProtKB:Q99JG2, ECO:0000269|PubMed:23690594, ECO:0000269|PubMed:27072655, ECO:0000269|PubMed:28688853}.
Ensembl transtripts involved in fusion geneENST idsENST00000591645, ENST00000300933, 
ENST00000344824, ENST00000538887, 
ENST00000367282, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score22 X 19 X 9=376212 X 6 X 7=504
# samples 2516
** MAII scorelog2(25/3762*10)=-3.91149984886111
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/504*10)=-1.65535182861255
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: TPM4 [Title/Abstract] AND GPR37L1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: TPM4 [Title/Abstract] AND GPR37L1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TPM4(16204563)-GPR37L1(202096868), # samples:1
Anticipated loss of major functional domain due to fusion event.TPM4-GPR37L1 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.
TPM4-GPR37L1 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
TgeneGPR37L1

GO:0007193

adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway

23690594

TgeneGPR37L1

GO:0043410

positive regulation of MAPK cascade

23690594



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/chr19:16204563/chr1:202096868)
- 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 TPM4 (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 GPR37L1 (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)
ENST00000344824TPM4chr1916204563+ENST00000367282GPR37L1chr1202096868+67428908211705294
ENST00000538887TPM4chr1916204563+ENST00000367282GPR37L1chr1202096868+67118597901674294
ENST00000300933TPM4chr1916204563+ENST00000367282GPR37L1chr1202096868+677692429973314

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
ENST00000344824ENST00000367282TPM4chr1916204563+GPR37L1chr1202096868+0.179311160.82068884
ENST00000538887ENST00000367282TPM4chr1916204563+GPR37L1chr1202096868+0.180046450.8199535
ENST00000300933ENST00000367282TPM4chr1916204563+GPR37L1chr1202096868+0.174652340.8253476

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 TPM4-GPR37L1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
TPM4chr1916204563GPR37L1chr120209686885923RLQNWKRQLMTWKVSSLGVTTFSLCA
TPM4chr1916204563GPR37L1chr120209686889023RLQNWKRQLMTWKVSSLGVTTFSLCA
TPM4chr1916204563GPR37L1chr1202096868924298TVAKLEKTIDDLEGLLSGSHDFQPLC

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Potential FusionNeoAntigen Information of TPM4-GPR37L1 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.
TPM4-GPR37L1_16204563_202096868.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)
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B13:02RQLMTWKV0.9820.7948614
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B52:01RQLMTWKV0.64380.9687614
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B08:01LMTWKVSSL0.98330.9778817
TPM4-GPR37L1chr1916204563chr1202096868924HLA-B15:17KTIDDLEGL0.9760.9547615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:22KTIDDLEGL0.96790.5324615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:60KTIDDLEGL0.96770.7026615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:30KTIDDLEGL0.96730.7285615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:67KTIDDLEGL0.96730.7285615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:24KTIDDLEGL0.96730.7285615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:17KTIDDLEGL0.9670.5071615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:04KTIDDLEGL0.96670.6447615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:21KTIDDLEGL0.96530.8181615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-B15:16KTIDDLEGL0.96230.8795615
TPM4-GPR37L1chr1916204563chr1202096868890HLA-A02:17LMTWKVSSL0.95460.6346817
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:29KTIDDLEGL0.90830.7262615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:20KTIDDLEGL0.88120.732615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-B57:03KTIDDLEGL0.82030.9955615
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:01KVSSLGVTTF0.99960.76121222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B57:01KVSSLGVTTF0.99880.88241222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:25KVSSLGVTTF0.99790.78171222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:17KVSSLGVTTF0.99780.77271222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:16KVSSLGVTTF0.99740.64351222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B57:03KVSSLGVTTF0.99610.87831222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B58:02KVSSLGVTTF0.9960.81971222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B58:01KVSSLGVTTF0.99380.8271222
TPM4-GPR37L1chr1916204563chr1202096868924HLA-B57:03KTIDDLEGLL0.97910.9937616
TPM4-GPR37L1chr1916204563chr1202096868890HLA-A32:13KVSSLGVTTF0.96420.71071222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B08:01QLMTWKVSSL0.95670.9693717
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B48:01RQLMTWKVSSL0.99620.8211617
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C08:15TIDDLEGL10.9673715
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C05:09TIDDLEGLL0.99980.9234716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C04:10TIDDLEGLL0.99970.8011716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C04:07TIDDLEGLL0.99950.8295716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C08:15TIDDLEGLL0.99950.9632716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C15:06KTIDDLEGL0.99920.9048615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C04:06TIDDLEGLL0.97060.9374716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:01KTIDDLEGL0.96730.7285615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C08:13TIDDLEGLL0.90810.9702716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C08:04TIDDLEGLL0.90810.9702716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:07TIDDLEGLL0.8090.7104716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C08:03TIDDLEGLL0.69740.9867716
TPM4-GPR37L1chr1916204563chr1202096868890HLA-C01:30LMTWKVSSL0.68040.984817
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C02:06KTIDDLEGL0.65980.9293615
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:07KVSSLGVTTF0.99940.5171222
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C08:02TIDDLEGL10.9673715
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C05:01TIDDLEGLL0.99980.9234716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C04:03TIDDLEGLL0.99980.8562716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C08:02TIDDLEGLL0.99950.9632716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C04:01TIDDLEGLL0.99950.8295716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C15:02KTIDDLEGL0.99930.8703615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C15:05KTIDDLEGL0.99920.9342615
TPM4-GPR37L1chr1916204563chr1202096868890HLA-A02:03LMTWKVSSL0.9910.8243817
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B08:18LMTWKVSSL0.98330.9778817
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:14KTIDDLEGL0.96570.6868615
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:06KTIDDLEGL0.96530.8181615
TPM4-GPR37L1chr1916204563chr1202096868890HLA-C06:08KRQLMTWKV0.90180.9417514
TPM4-GPR37L1chr1916204563chr1202096868924HLA-B57:02KTIDDLEGL0.87140.8809615
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B08:12LMTWKVSSL0.86630.9873817
TPM4-GPR37L1chr1916204563chr1202096868890HLA-C01:03LMTWKVSSL0.84170.9608817
TPM4-GPR37L1chr1916204563chr1202096868890HLA-C01:02LMTWKVSSL0.78340.9815817
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C08:01TIDDLEGLL0.69740.9867716
TPM4-GPR37L1chr1916204563chr1202096868924HLA-C17:01KTIDDLEGL0.640.8769615
TPM4-GPR37L1chr1916204563chr1202096868890HLA-C07:22KRQLMTWKV0.440.6269514
TPM4-GPR37L1chr1916204563chr1202096868890HLA-C06:02KRQLMTWKV0.01250.9434514
TPM4-GPR37L1chr1916204563chr1202096868890HLA-C06:17KRQLMTWKV0.01250.9434514
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:34KVSSLGVTTF0.99960.76121222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:135KVSSLGVTTF0.99960.76551222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:125KVSSLGVTTF0.99960.76121222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:33KVSSLGVTTF0.99960.76121222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:27KVSSLGVTTF0.99960.77011222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:50KVSSLGVTTF0.99950.70581222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:24KVSSLGVTTF0.99940.73251222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:35KVSSLGVTTF0.99940.6651222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B57:04KVSSLGVTTF0.99890.59131222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B57:10KVSSLGVTTF0.99880.88241222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B58:06KVSSLGVTTF0.99850.65811222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B15:39KVSSLGVTTF0.99770.72811222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-A32:01KVSSLGVTTF0.9950.77711222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B57:02KVSSLGVTTF0.98970.83311222
TPM4-GPR37L1chr1916204563chr1202096868890HLA-B08:18QLMTWKVSSL0.95670.9693717
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A02:14KTIDDLEGLL0.92570.6885616
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A68:02EKTIDDLEGL0.75360.6215515
TPM4-GPR37L1chr1916204563chr1202096868924HLA-A69:01EKTIDDLEGL0.56610.8148515

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Potential FusionNeoAntigen Information of TPM4-GPR37L1 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.

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)

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Fusion breakpoint peptide structures of TPM4-GPR37L1

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
4631KTIDDLEGLLSGSHTPM4GPR37L1chr1916204563chr1202096868924
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
8130RQLMTWKVSSLGVTTPM4GPR37L1chr1916204563chr1202096868890

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of TPM4-GPR37L1

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-B14:023BVN4631KTIDDLEGLLSGSH-7.15543-7.26883
HLA-B14:023BVN4631KTIDDLEGLLSGSH-4.77435-5.80965
HLA-B52:013W394631KTIDDLEGLLSGSH-6.80875-6.92215
HLA-B52:013W394631KTIDDLEGLLSGSH-4.20386-5.23916
HLA-A11:014UQ24631KTIDDLEGLLSGSH-7.5194-8.5547
HLA-A11:014UQ24631KTIDDLEGLLSGSH-6.9601-7.0735
HLA-A24:025HGA4631KTIDDLEGLLSGSH-7.52403-7.63743
HLA-A24:025HGA4631KTIDDLEGLLSGSH-5.82433-6.85963
HLA-B27:056PYJ4631KTIDDLEGLLSGSH-3.28285-4.31815
HLA-B44:053DX84631KTIDDLEGLLSGSH-5.91172-6.94702
HLA-B44:053DX84631KTIDDLEGLLSGSH-4.24346-4.35686
HLA-B14:023BVN8130RQLMTWKVSSLGVT-7.15543-7.26883
HLA-B14:023BVN8130RQLMTWKVSSLGVT-4.77435-5.80965
HLA-B52:013W398130RQLMTWKVSSLGVT-6.80875-6.92215
HLA-B52:013W398130RQLMTWKVSSLGVT-4.20386-5.23916
HLA-A11:014UQ28130RQLMTWKVSSLGVT-7.5194-8.5547
HLA-A11:014UQ28130RQLMTWKVSSLGVT-6.9601-7.0735
HLA-A24:025HGA8130RQLMTWKVSSLGVT-7.52403-7.63743
HLA-A24:025HGA8130RQLMTWKVSSLGVT-5.82433-6.85963
HLA-B27:056PYJ8130RQLMTWKVSSLGVT-3.28285-4.31815
HLA-B44:053DX88130RQLMTWKVSSLGVT-5.91172-6.94702
HLA-B44:053DX88130RQLMTWKVSSLGVT-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of TPM4-GPR37L1

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
TPM4-GPR37L1chr1916204563chr12020968681222KVSSLGVTTFAAGGTCTCCTCTCTGGGAGTCACGACTTTC
TPM4-GPR37L1chr1916204563chr1202096868514KRQLMTWKVAAAAGACAATTGATGACCTGGAAGGTC
TPM4-GPR37L1chr1916204563chr1202096868515EKTIDDLEGLAAAAGACAATTGATGACCTGGAAGGTCTCC
TPM4-GPR37L1chr1916204563chr1202096868614RQLMTWKVAGACAATTGATGACCTGGAAGGTC
TPM4-GPR37L1chr1916204563chr1202096868615KTIDDLEGLAGACAATTGATGACCTGGAAGGTCTCC
TPM4-GPR37L1chr1916204563chr1202096868616KTIDDLEGLLAGACAATTGATGACCTGGAAGGTCTCCTCT
TPM4-GPR37L1chr1916204563chr1202096868617RQLMTWKVSSLAGACAATTGATGACCTGGAAGGTCTCCTCTCTG
TPM4-GPR37L1chr1916204563chr1202096868715TIDDLEGLCAATTGATGACCTGGAAGGTCTCC
TPM4-GPR37L1chr1916204563chr1202096868716TIDDLEGLLCAATTGATGACCTGGAAGGTCTCCTCT
TPM4-GPR37L1chr1916204563chr1202096868717QLMTWKVSSLCAATTGATGACCTGGAAGGTCTCCTCTCTG
TPM4-GPR37L1chr1916204563chr1202096868817LMTWKVSSLTTGATGACCTGGAAGGTCTCCTCTCTG

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

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Information of the samples that have these potential fusion neoantigens of TPM4-GPR37L1

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
UCECTPM4-GPR37L1chr1916204563ENST00000300933chr1202096868ENST00000367282TCGA-D1-A16R
UCECTPM4-GPR37L1chr1916204563ENST00000344824chr1202096868ENST00000367282TCGA-D1-A16R

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Potential target of CAR-T therapy development for TPM4-GPR37L1

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
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202252_2720482.0TransmembraneHelical%3B Name%3D4
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202311_3310482.0TransmembraneHelical%3B Name%3D5
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202362_3820482.0TransmembraneHelical%3B Name%3D6
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202399_4190482.0TransmembraneHelical%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 TPM4-GPR37L1

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 TPM4-GPR37L1

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
HgeneTPM4C0001787Osteoporosis, Age-Related1CTD_human
HgeneTPM4C0003949Asbestosis1CTD_human
HgeneTPM4C0005818Blood Platelet Disorders1GENOMICS_ENGLAND
HgeneTPM4C0014859Esophageal Neoplasms1CTD_human
HgeneTPM4C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneTPM4C0027627Neoplasm Metastasis1CTD_human
HgeneTPM4C0029456Osteoporosis1CTD_human
HgeneTPM4C0029459Osteoporosis, Senile1CTD_human
HgeneTPM4C0032927Precancerous Conditions1CTD_human
HgeneTPM4C0043094Weight Gain1CTD_human
HgeneTPM4C0282313Condition, Preneoplastic1CTD_human
HgeneTPM4C0334121Inflammatory Myofibroblastic Tumor1ORPHANET
HgeneTPM4C0546837Malignant neoplasm of esophagus1CTD_human
HgeneTPM4C0751406Post-Traumatic Osteoporosis1CTD_human
HgeneTPM4C0948089Acute Coronary Syndrome1CTD_human
HgeneTPM4C2751260Macrothrombocytopenia1GENOMICS_ENGLAND
HgeneTPM4C2930617Pulmonary Fibrosis - from Asbestos Exposure1CTD_human
HgeneTPM4C4304021Autosomal dominant macrothrombocytopenia1ORPHANET