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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:TPM4-GPR37L1

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

O60883

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
Context (manual curation of fusion genes in FusionPDB)

PubMed: TPM4 [Title/Abstract] AND GPR37L1 [Title/Abstract] AND fusion [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 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 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
ChimerDB4UCECTCGA-D1-A16RTPM4chr19

16204563

+GPR37L1chr1

202096868

+


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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)
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

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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

>93402_93402_1_TPM4-GPR37L1_TPM4_chr19_16204563_ENST00000300933_GPR37L1_chr1_202096868_ENST00000367282_length(amino acids)=314AA_BP=298
MWPAVPTSGPPPAVLTSAVRPGDLIAPTAAGPGGGERRGRPPRRQRLGGPGRGCAALAGAEPSRASAAARAPLRLRAMAGLNSLEAVKRK
IQALQQQADEAEDRAQGLQRELDGERERREKAEGDVAALNRRIQLVEEELDRAQERLATALQKLEEAEKAADESERGMKVIENRAMKDEE
KMEIQEMQLKEAKHIAEEADRKYEEVARKLVILEGELERAEERAEVSELKCGDLEEELKNVTNNLKSLEAASEKYSEKEDKYEEEIKLLS

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

>93402_93402_2_TPM4-GPR37L1_TPM4_chr19_16204563_ENST00000344824_GPR37L1_chr1_202096868_ENST00000367282_length(amino acids)=294AA_BP=23
MRPVLNLQRERLQNWKRQLMTWKVSSLGVTTFSLCALGIDRFHVATSTLPKVRPIERCQSILAKLAVIWVGSMTLAVPELLLWQLAQEPA
PTMGTLDSCIMKPSASLPESLYSLVMTYQNARMWWYFGCYFCLPILFTVTCQLVTWRVRGPPGRKSECRASKHEQCESQLNSTVVGLTVV
YAFCTLPENVCNIVVAYLSTELTRQTLDLLGLINQFSTFFKGAITPVLLLCICRPLGQAFLDCCCCCCCEECGGASEASAANGSDNKLKT

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

>93402_93402_3_TPM4-GPR37L1_TPM4_chr19_16204563_ENST00000538887_GPR37L1_chr1_202096868_ENST00000367282_length(amino acids)=294AA_BP=23
MRPVLNLQRERLQNWKRQLMTWKVSSLGVTTFSLCALGIDRFHVATSTLPKVRPIERCQSILAKLAVIWVGSMTLAVPELLLWQLAQEPA
PTMGTLDSCIMKPSASLPESLYSLVMTYQNARMWWYFGCYFCLPILFTVTCQLVTWRVRGPPGRKSECRASKHEQCESQLNSTVVGLTVV
YAFCTLPENVCNIVVAYLSTELTRQTLDLLGLINQFSTFFKGAITPVLLLCICRPLGQAFLDCCCCCCCEECGGASEASAANGSDNKLKT

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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/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 buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TPM4

P67936

GPR37L1

O60883

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}.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}.

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
HgeneTPM4chr19:16204563chr1:202096868ENST00000344824+892_248257.3333333333333285.0Coiled coilOntology_term=ECO:0000250
HgeneTPM4chr19:16204563chr1:202096868ENST00000538887+8102_248257.3333333333333270.0Coiled coilOntology_term=ECO:0000250
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202418_439210.0482.0Compositional biasNote=Cys-rich
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202227_251210.0482.0Topological domainCytoplasmic
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202273_310210.0482.0Topological domainExtracellular
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202332_361210.0482.0Topological domainCytoplasmic
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202383_398210.0482.0Topological domainExtracellular
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202420_481210.0482.0Topological domainCytoplasmic
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202252_272210.0482.0TransmembraneHelical%3B Name%3D4
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202311_331210.0482.0TransmembraneHelical%3B Name%3D5
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202362_382210.0482.0TransmembraneHelical%3B Name%3D6
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202399_419210.0482.0TransmembraneHelical%3B Name%3D7

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneTPM4chr19:16204563chr1:202096868ENST00000300933+782_248221.33333333333334249.0Coiled coilOntology_term=ECO:0000250
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202156_167210.0482.0Topological domainCytoplasmic
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202189_205210.0482.0Topological domainExtracellular
TgeneGPR37L1chr19:16204563chr1:202096868ENST000003672820226_134210.0482.0Topological domainExtracellular
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202135_155210.0482.0TransmembraneHelical%3B Name%3D1
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202168_188210.0482.0TransmembraneHelical%3B Name%3D2
TgeneGPR37L1chr19:16204563chr1:202096868ENST0000036728202206_226210.0482.0TransmembraneHelical%3B Name%3D3


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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
TPM4TCERG1, TRIP6, PACSIN1, ARRB1, SP1, CDK2, AKT1, TPM3, TPM2, TPM1, SRXN1, HNRNPK, DBN1, ZYX, PCMT1, G3BP1, PSMD2, PSMA6, CDH2, SULT1A1, SERPINH1, ILF3, ILF2, TELO2, MYH9, PSMD1, SNRNP70, TXN2, SRSF2, PRKCDBP, CORO1C, TPM3P4, DCTN2, PSMC2, ATF2, PAN2, HDAC8, PARK2, CAP1, FASN, KIAA1598, SIRT1, TP53, LNX1, PYCARD, EGFR, ACTN1, ACTN2, COX5A, OSTF1, ACTN4, ATP1A1, ATP5F1, CENPE, CKB, COX4I1, MYH7B, NDUFB10, PSMA1, TBCD, NTRK1, ADD1, CAPZA2, FLNA, PPP1CB, PPP1CC, IQGAP1, SLC33A1, PDLIM7, MAPRE1, ANLN, MYO19, MYO18A, CFAP97, Actb, Mapre1, Flot1, Myh9, Myo1c, Rab5c, Tpm1, Dctn3, Uso1, Anapc13, Calml3, 2510003E04Rik, Myh10, Tbck, Mast3, MCM2, SMURF1, ZNF131, DLST, UBE2A, CFTR, TMPO, PTPLA, PPP6C, PPM1D, PTP4A3, PTPN2, CDC25C, PTPRCAP, DUSP7, PPTC7, DUSP19, PPM1M, ILKAP, DUSP21, PHPT1, DUSP12, PPP1R3C, EFTUD2, PIH1D1, TNF, NOD2, RNF181, RNF144A, CDK9, RAB9A, HK1, METTL14, WTAP, ATG16L1, ESR2, DISC1, USP14, APEX1, DYRK1A, SCARB2, VMP1, AKT3, ATF3, PICK1, SNAPIN, JRK, CUL7, PLEKHA4, SRC, UNK, CIT, AURKB, CHMP4C, ECT2, KIF20A, PRNP, MFN2, OPA1, HNRNPH1, nsp13ab, NPC1, UCHL1, COPS5, DANCR, RIN3, TRIM24, BAG5, AR, ISG15, TMOD1, TRIM37, NAA40, MRPL50, LANCL2, ALAD, BTF3, TRIM26, EP300, CTSB, CTSS, DPP4, E, ORF8, TMPRSS2, TOP3B, CTSL, FURIN, IFITM1, IFITM3, CLEC4D, CLEC4E, nsp4, nsp6, nsp8, ORF10, S, FGD5, CCNF, PDE4B, FOS, ELK3, GATA4, IRF8, KLF10, KLF12, KLF3, KLF6, VSX1, ZIC3, MYC, NKX2-5, SOX5, STAT5B, TEAD1, TLX1,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
TPM4all structure
GPR37L1


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 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