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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:PLEKHH1-GPHN

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PLEKHH1-GPHN
FusionPDB ID: 66287
FusionGDB2.0 ID: 66287
HgeneTgene
Gene symbol

PLEKHH1

GPHN

Gene ID

57475

10243

Gene namepleckstrin homology, MyTH4 and FERM domain containing H1gephyrin
Synonyms-GEPH|GPH|GPHRYN|HKPX1|MOCODC
Cytomap

14q24.1

14q23.3-q24.1

Type of geneprotein-codingprotein-coding
Descriptionpleckstrin homology domain-containing family H member 1PH domain-containing family H member 1pleckstrin homology domain containing, family H (with MyTH4 domain) member 1gephyrin
Modification date2020031320200313
UniProtAcc.

Q9NQX3

Ensembl transtripts involved in fusion geneENST idsENST00000329153, ENST00000417684, 
ENST00000559832, 
ENST00000544752, 
ENST00000459628, ENST00000305960, 
ENST00000315266, ENST00000478722, 
ENST00000543237, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 8 X 4=28842 X 51 X 15=32130
# samples 1162
** MAII scorelog2(11/288*10)=-1.38856528791765
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(62/32130*10)=-5.69550895508454
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: PLEKHH1 [Title/Abstract] AND GPHN [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PLEKHH1(68028752)-GPHN(67525366), # samples:3
Anticipated loss of major functional domain due to fusion event.PLEKHH1-GPHN 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.
PLEKHH1-GPHN 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.
PLEKHH1-GPHN 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.
PLEKHH1-GPHN 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.
PLEKHH1-GPHN seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PLEKHH1-GPHN seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PLEKHH1-GPHN seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted 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
TgeneGPHN

GO:0032324

molybdopterin cofactor biosynthetic process

26613940

TgeneGPHN

GO:0097112

gamma-aminobutyric acid receptor clustering

26613940


check buttonFusion gene breakpoints across PLEKHH1 (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 GPHN (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
ChimerDB4BLCATCGA-K4-A3WV-01APLEKHH1chr14

68028752

-GPHNchr14

67525366

+
ChimerDB4BLCATCGA-K4-A3WV-01APLEKHH1chr14

68028752

+GPHNchr14

67525366

+


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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)
ENST00000329153PLEKHH1chr1468028752+ENST00000315266GPHNchr1467525366+2802637301940636
ENST00000329153PLEKHH1chr1468028752+ENST00000478722GPHNchr1467525366+2807637301940636
ENST00000329153PLEKHH1chr1468028752+ENST00000543237GPHNchr1467525366+2027637301940636
ENST00000329153PLEKHH1chr1468028752+ENST00000305960GPHNchr1467525366+2201637301940636

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
ENST00000329153ENST00000315266PLEKHH1chr1468028752+GPHNchr1467525366+0.0023850020.997615
ENST00000329153ENST00000478722PLEKHH1chr1468028752+GPHNchr1467525366+0.0022994550.9977005
ENST00000329153ENST00000543237PLEKHH1chr1468028752+GPHNchr1467525366+0.0076291410.99237084
ENST00000329153ENST00000305960PLEKHH1chr1468028752+GPHNchr1467525366+0.0054343120.9945657

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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

>66287_66287_1_PLEKHH1-GPHN_PLEKHH1_chr14_68028752_ENST00000329153_GPHN_chr14_67525366_ENST00000305960_length(amino acids)=636AA_BP=202
MRRRPEGARVPSARRGRPRARWRAPQNNPEVDSIMAELKVEAPASVDWQKRCLTLETQLFRFRLQASKIRELLADKMQELEQRLLEAEQR
AENAETQVGVMEEKVKLSNLKNVDSEGSLHRKYQELLKAIKGKDELISQLEAQLEKQKQMRAEEAKTVQEKAAKIKEWVTLKLAKLEMEN
QHLKSHNQRLVEQVGSLQDALEGHSAVDITKVARRHRMSPFPLTSMDKAFITVLEMTPVLGTEIINYRDGMGRVLAQDVYAKDNLPPFPA
SVKDGYAVRAADGPGDRFIIGESQAGEQPTQTVMPGQVMRVTTGAPIPCGADAVVQVEDTELIRESDDGTEELEVRILVQARPGQDIRPI
GHDIKRGECVLAKGTHMGPSEIGLLATVGVTEVEVNKFPVVAVMSTGNELLNPEDDLLPGKIRDSNRSTLLATIQEHGYPTINLGIVGDN
PDDLLNALNEGISRADVIITSGGVSMGEKDYLKQVLDIDLHAQIHFGRVFMKPGLPTTFATLDIDGVRKIIFALPGNPVSAVVTCNLFVV
PALRKMQGILDPRPTIIKARLSCDVKLDPRPEYHRCILTWHHQEPLPWAQSTGNQMSSRLMSMRSANGLLMLPPKTEQYVELHKGEVVDV

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

>66287_66287_2_PLEKHH1-GPHN_PLEKHH1_chr14_68028752_ENST00000329153_GPHN_chr14_67525366_ENST00000315266_length(amino acids)=636AA_BP=202
MRRRPEGARVPSARRGRPRARWRAPQNNPEVDSIMAELKVEAPASVDWQKRCLTLETQLFRFRLQASKIRELLADKMQELEQRLLEAEQR
AENAETQVGVMEEKVKLSNLKNVDSEGSLHRKYQELLKAIKGKDELISQLEAQLEKQKQMRAEEAKTVQEKAAKIKEWVTLKLAKLEMEN
QHLKSHNQRLVEQVGSLQDALEGHSAVDITKVARRHRMSPFPLTSMDKAFITVLEMTPVLGTEIINYRDGMGRVLAQDVYAKDNLPPFPA
SVKDGYAVRAADGPGDRFIIGESQAGEQPTQTVMPGQVMRVTTGAPIPCGADAVVQVEDTELIRESDDGTEELEVRILVQARPGQDIRPI
GHDIKRGECVLAKGTHMGPSEIGLLATVGVTEVEVNKFPVVAVMSTGNELLNPEDDLLPGKIRDSNRSTLLATIQEHGYPTINLGIVGDN
PDDLLNALNEGISRADVIITSGGVSMGEKDYLKQVLDIDLHAQIHFGRVFMKPGLPTTFATLDIDGVRKIIFALPGNPVSAVVTCNLFVV
PALRKMQGILDPRPTIIKARLSCDVKLDPRPEYHRCILTWHHQEPLPWAQSTGNQMSSRLMSMRSANGLLMLPPKTEQYVELHKGEVVDV

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

>66287_66287_3_PLEKHH1-GPHN_PLEKHH1_chr14_68028752_ENST00000329153_GPHN_chr14_67525366_ENST00000478722_length(amino acids)=636AA_BP=202
MRRRPEGARVPSARRGRPRARWRAPQNNPEVDSIMAELKVEAPASVDWQKRCLTLETQLFRFRLQASKIRELLADKMQELEQRLLEAEQR
AENAETQVGVMEEKVKLSNLKNVDSEGSLHRKYQELLKAIKGKDELISQLEAQLEKQKQMRAEEAKTVQEKAAKIKEWVTLKLAKLEMEN
QHLKSHNQRLVEQVGSLQDALEGHSAVDITKVARRHRMSPFPLTSMDKAFITVLEMTPVLGTEIINYRDGMGRVLAQDVYAKDNLPPFPA
SVKDGYAVRAADGPGDRFIIGESQAGEQPTQTVMPGQVMRVTTGAPIPCGADAVVQVEDTELIRESDDGTEELEVRILVQARPGQDIRPI
GHDIKRGECVLAKGTHMGPSEIGLLATVGVTEVEVNKFPVVAVMSTGNELLNPEDDLLPGKIRDSNRSTLLATIQEHGYPTINLGIVGDN
PDDLLNALNEGISRADVIITSGGVSMGEKDYLKQVLDIDLHAQIHFGRVFMKPGLPTTFATLDIDGVRKIIFALPGNPVSAVVTCNLFVV
PALRKMQGILDPRPTIIKARLSCDVKLDPRPEYHRCILTWHHQEPLPWAQSTGNQMSSRLMSMRSANGLLMLPPKTEQYVELHKGEVVDV

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

>66287_66287_4_PLEKHH1-GPHN_PLEKHH1_chr14_68028752_ENST00000329153_GPHN_chr14_67525366_ENST00000543237_length(amino acids)=636AA_BP=202
MRRRPEGARVPSARRGRPRARWRAPQNNPEVDSIMAELKVEAPASVDWQKRCLTLETQLFRFRLQASKIRELLADKMQELEQRLLEAEQR
AENAETQVGVMEEKVKLSNLKNVDSEGSLHRKYQELLKAIKGKDELISQLEAQLEKQKQMRAEEAKTVQEKAAKIKEWVTLKLAKLEMEN
QHLKSHNQRLVEQVGSLQDALEGHSAVDITKVARRHRMSPFPLTSMDKAFITVLEMTPVLGTEIINYRDGMGRVLAQDVYAKDNLPPFPA
SVKDGYAVRAADGPGDRFIIGESQAGEQPTQTVMPGQVMRVTTGAPIPCGADAVVQVEDTELIRESDDGTEELEVRILVQARPGQDIRPI
GHDIKRGECVLAKGTHMGPSEIGLLATVGVTEVEVNKFPVVAVMSTGNELLNPEDDLLPGKIRDSNRSTLLATIQEHGYPTINLGIVGDN
PDDLLNALNEGISRADVIITSGGVSMGEKDYLKQVLDIDLHAQIHFGRVFMKPGLPTTFATLDIDGVRKIIFALPGNPVSAVVTCNLFVV
PALRKMQGILDPRPTIIKARLSCDVKLDPRPEYHRCILTWHHQEPLPWAQSTGNQMSSRLMSMRSANGLLMLPPKTEQYVELHKGEVVDV

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

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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/chr14:68028752/chr14:67525366)
- 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
.GPHN

Q9NQX3

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.FUNCTION: Microtubule-associated protein involved in membrane protein-cytoskeleton interactions. It is thought to anchor the inhibitory glycine receptor (GLYR) to subsynaptic microtubules (By similarity). Acts as a major instructive molecule at inhibitory synapses, where it also clusters GABA type A receptors (PubMed:25025157, PubMed:26613940). {ECO:0000250|UniProtKB:Q03555, ECO:0000269|PubMed:25025157, ECO:0000269|PubMed:26613940}.; FUNCTION: Has also a catalytic activity and catalyzes two steps in the biosynthesis of the molybdenum cofactor. In the first step, molybdopterin is adenylated. Subsequently, molybdate is inserted into adenylated molybdopterin and AMP is released. {ECO:0000269|PubMed:26613940}.

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
HgenePLEKHH1chr14:68028752chr14:67525366ENST00000329153+62928_169168.333333333333341365.0Coiled coilOntology_term=ECO:0000255
TgeneGPHNchr14:68028752chr14:67525366ENST00000315266822326_736302.3333333333333737.0RegionNote=MPT adenylyltransferase

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgenePLEKHH1chr14:68028752chr14:67525366ENST00000329153+629239_242168.333333333333341365.0Compositional biasNote=Poly-Ser
HgenePLEKHH1chr14:68028752chr14:67525366ENST00000329153+629578_672168.333333333333341365.0DomainPH 1
HgenePLEKHH1chr14:68028752chr14:67525366ENST00000329153+629687_796168.333333333333341365.0DomainPH 2
HgenePLEKHH1chr14:68028752chr14:67525366ENST00000329153+629832_986168.333333333333341365.0DomainMyTH4
HgenePLEKHH1chr14:68028752chr14:67525366ENST00000329153+629997_1333168.333333333333341365.0DomainFERM
TgeneGPHNchr14:68028752chr14:67525366ENST0000031526682214_166302.3333333333333737.0RegionNote=MPT Mo-transferase
TgeneGPHNchr14:68028752chr14:67525366ENST0000047872292314_166335.3333333333333770.0RegionNote=MPT Mo-transferase
TgeneGPHNchr14:68028752chr14:67525366ENST00000478722923326_736335.3333333333333770.0RegionNote=MPT adenylyltransferase


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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
PLEKHH1
GPHNall structure


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
TgeneGPHNchr14:68028752chr14:67525366ENST00000315266822140_316302.3333333333333737.0GABARAP
TgeneGPHNchr14:68028752chr14:67525366ENST00000478722923140_316335.3333333333333770.0GABARAP


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Related Drugs to PLEKHH1-GPHN


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 PLEKHH1-GPHN


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
TgeneGPHNC1854990Molybdenum Cofactor Deficiency, Complementation Group C5CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneGPHNC0001956Alcohol Use Disorder1CTD_human
TgeneGPHNC0001973Alcoholic Intoxication, Chronic1CTD_human
TgeneGPHNC0009171Cocaine Abuse1CTD_human
TgeneGPHNC0085762Alcohol abuse1CTD_human
TgeneGPHNC0236736Cocaine-Related Disorders1CTD_human
TgeneGPHNC0543888Epileptic encephalopathy1GENOMICS_ENGLAND
TgeneGPHNC0600427Cocaine Dependence1CTD_human