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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:SSR3-CLU

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SSR3-CLU
FusionPDB ID: 86844
FusionGDB2.0 ID: 86844
HgeneTgene
Gene symbol

SSR3

CLU

Gene ID

6747

1191

Gene namesignal sequence receptor subunit 3clusterin
SynonymsTRAPGAAG4|APO-J|APOJ|CLI|CLU1|CLU2|KUB1|NA1/NA2|SGP-2|SGP2|SP-40|TRPM-2|TRPM2
Cytomap

3q25.31

8p21.1

Type of geneprotein-codingprotein-coding
Descriptiontranslocon-associated protein subunit gammaSSR gammaTRAP-complex gamma subunitTRAP-gammasignal sequence receptor subunit gammasignal sequence receptor, gamma (translocon-associated protein gamma)translocon-associated protein gamma subunitclusterinaging-associated protein 4apolipoprotein Jcomplement cytolysis inhibitorcomplement lysis inhibitorcomplement-associated protein SP-40,40epididymis secretory sperm binding proteinku70-binding protein 1sulfated glycoprotein 2testosterone-r
Modification date2020031320200327
UniProtAcc.

Q15846

Ensembl transtripts involved in fusion geneENST idsENST00000265044, ENST00000463503, 
ENST00000467789, ENST00000476217, 
ENST00000496050, ENST00000478842, 
ENST00000316403, ENST00000405140, 
ENST00000546343, ENST00000523500, 
ENST00000560366, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 7 X 4=19623 X 24 X 12=6624
# samples 730
** MAII scorelog2(7/196*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(30/6624*10)=-4.46466826700344
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: SSR3 [Title/Abstract] AND CLU [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SSR3(156271443)-CLU(27455767), # samples:1
Anticipated loss of major functional domain due to fusion event.SSR3-CLU 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.
SSR3-CLU 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.
SSR3-CLU seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
SSR3-CLU seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SSR3-CLU seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
TgeneCLU

GO:0000902

cell morphogenesis

15857407

TgeneCLU

GO:0001774

microglial cell activation

15857407

TgeneCLU

GO:0017038

protein import

24446231

TgeneCLU

GO:0031333

negative regulation of protein complex assembly

22179788|23106396

TgeneCLU

GO:0031334

positive regulation of protein complex assembly

22179788

TgeneCLU

GO:0032760

positive regulation of tumor necrosis factor production

15857407

TgeneCLU

GO:0045429

positive regulation of nitric oxide biosynthetic process

15857407

TgeneCLU

GO:0050821

protein stabilization

11123922|12176985

TgeneCLU

GO:0051131

chaperone-mediated protein complex assembly

17412999

TgeneCLU

GO:0051788

response to misfolded protein

19996109

TgeneCLU

GO:0061077

chaperone-mediated protein folding

11123922

TgeneCLU

GO:0061518

microglial cell proliferation

15857407

TgeneCLU

GO:1900221

regulation of amyloid-beta clearance

24446231

TgeneCLU

GO:1901214

regulation of neuron death

17412999

TgeneCLU

GO:1901216

positive regulation of neuron death

15857407

TgeneCLU

GO:1902430

negative regulation of amyloid-beta formation

12047389|17412999

TgeneCLU

GO:1905907

negative regulation of amyloid fibril formation

22179788


check buttonFusion gene breakpoints across SSR3 (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 CLU (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
ChimerDB4OVTCGA-04-1536SSR3chr3

156271443

-CLUchr8

27455767

-


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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)
ENST00000265044SSR3chr3156271443-ENST00000560366CLUchr827455767-167135541364107
ENST00000265044SSR3chr3156271443-ENST00000523500CLUchr827455767-61035541364107
ENST00000467789SSR3chr3156271443-ENST00000560366CLUchr827455767-16363206329107
ENST00000467789SSR3chr3156271443-ENST00000523500CLUchr827455767-5753206329107
ENST00000476217SSR3chr3156271443-ENST00000560366CLUchr827455767-16122961078764104
ENST00000476217SSR3chr3156271443-ENST00000523500CLUchr827455767-5512963630589
ENST00000463503SSR3chr3156271443-ENST00000546343CLUchr827455767-15522361018704104
ENST00000496050SSR3chr3156271443-ENST00000546343CLUchr827455767-15762601042728104

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
ENST00000265044ENST00000560366SSR3chr3156271443-CLUchr827455767-0.047769070.95223093
ENST00000265044ENST00000523500SSR3chr3156271443-CLUchr827455767-0.036377030.963623
ENST00000467789ENST00000560366SSR3chr3156271443-CLUchr827455767-0.0877365840.91226345
ENST00000467789ENST00000523500SSR3chr3156271443-CLUchr827455767-0.0368797560.9631203
ENST00000476217ENST00000560366SSR3chr3156271443-CLUchr827455767-0.114467050.885533
ENST00000476217ENST00000523500SSR3chr3156271443-CLUchr827455767-0.061408840.9385912
ENST00000463503ENST00000546343SSR3chr3156271443-CLUchr827455767-0.82586940.1741306
ENST00000496050ENST00000546343SSR3chr3156271443-CLUchr827455767-0.732797440.2672026

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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

>86844_86844_1_SSR3-CLU_SSR3_chr3_156271443_ENST00000265044_CLU_chr8_27455767_ENST00000523500_length(amino acids)=107AA_BP=
MPALAAGSTFPVLACSSAMAPKGSSKQQSEEDLLLQDFSRNLSAKSSALFFGNAFIVSAIPIWLYWRIWHMDLIQSAVLYSVMTLVSTYL

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

>86844_86844_2_SSR3-CLU_SSR3_chr3_156271443_ENST00000265044_CLU_chr8_27455767_ENST00000560366_length(amino acids)=107AA_BP=
MPALAAGSTFPVLACSSAMAPKGSSKQQSEEDLLLQDFSRNLSAKSSALFFGNAFIVSAIPIWLYWRIWHMDLIQSAVLYSVMTLVSTYL

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

>86844_86844_3_SSR3-CLU_SSR3_chr3_156271443_ENST00000463503_CLU_chr8_27455767_ENST00000546343_length(amino acids)=104AA_BP=
MLSSYNSKSTAFTNKTAAKAIALTNKTDNLDFWAPNVFITKTSIMHYNTKYTLHLLILLLNFQCIPLGDCRTLVRIHRQFYNRTEKLPFA

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

>86844_86844_4_SSR3-CLU_SSR3_chr3_156271443_ENST00000467789_CLU_chr8_27455767_ENST00000523500_length(amino acids)=107AA_BP=
MPALAAGSTFPVLACSSAMAPKGSSKQQSEEDLLLQDFSRNLSAKSSALFFGNAFIVSAIPIWLYWRIWHMDLIQSAVLYSVMTLVSTYL

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

>86844_86844_5_SSR3-CLU_SSR3_chr3_156271443_ENST00000467789_CLU_chr8_27455767_ENST00000560366_length(amino acids)=107AA_BP=
MPALAAGSTFPVLACSSAMAPKGSSKQQSEEDLLLQDFSRNLSAKSSALFFGNAFIVSAIPIWLYWRIWHMDLIQSAVLYSVMTLVSTYL

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

>86844_86844_6_SSR3-CLU_SSR3_chr3_156271443_ENST00000476217_CLU_chr8_27455767_ENST00000523500_length(amino acids)=89AA_BP=

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

>86844_86844_7_SSR3-CLU_SSR3_chr3_156271443_ENST00000476217_CLU_chr8_27455767_ENST00000560366_length(amino acids)=104AA_BP=
MLSSYNSKSTAFTNKTAAKAIALTNKTDNLDFWAPNVFITKTSIMHYNTKYTLHLLILLLNFQCIPLGDCRTLVRIHRQFYNRTEKLPFA

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

>86844_86844_8_SSR3-CLU_SSR3_chr3_156271443_ENST00000496050_CLU_chr8_27455767_ENST00000546343_length(amino acids)=104AA_BP=
MLSSYNSKSTAFTNKTAAKAIALTNKTDNLDFWAPNVFITKTSIMHYNTKYTLHLLILLLNFQCIPLGDCRTLVRIHRQFYNRTEKLPFA

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

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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/chr3:156271443/chr8:27455767)
- 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
.CLU

Q15846

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.

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
HgeneSSR3chr3:156271443chr8:27455767ENST00000265044-251_2786.66666666666667186.0Topological domainLumenal
HgeneSSR3chr3:156271443chr8:27455767ENST00000265044-2549_5486.66666666666667186.0Topological domainCytoplasmic
HgeneSSR3chr3:156271443chr8:27455767ENST00000265044-2528_4886.66666666666667186.0TransmembraneHelical
HgeneSSR3chr3:156271443chr8:27455767ENST00000265044-2555_7686.66666666666667186.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSSR3chr3:156271443chr8:27455767ENST00000265044-25158_16386.66666666666667186.0Topological domainCytoplasmic
HgeneSSR3chr3:156271443chr8:27455767ENST00000265044-2577_13586.66666666666667186.0Topological domainLumenal
HgeneSSR3chr3:156271443chr8:27455767ENST00000265044-25136_15786.66666666666667186.0TransmembraneHelical
HgeneSSR3chr3:156271443chr8:27455767ENST00000265044-25164_18486.66666666666667186.0TransmembraneHelical
TgeneCLUchr3:156271443chr8:27455767ENST0000031640379443_447446.6666666666667450.0MotifNuclear localization signal
TgeneCLUchr3:156271443chr8:27455767ENST000003164037978_81446.6666666666667450.0MotifNuclear localization signal
TgeneCLUchr3:156271443chr8:27455767ENST0000040514079443_447446.6666666666667450.0MotifNuclear localization signal
TgeneCLUchr3:156271443chr8:27455767ENST000004051407978_81446.6666666666667450.0MotifNuclear localization signal
TgeneCLUchr3:156271443chr8:27455767ENST0000052350068443_447446.6666666666667450.0MotifNuclear localization signal
TgeneCLUchr3:156271443chr8:27455767ENST000005235006878_81446.6666666666667450.0MotifNuclear localization signal
TgeneCLUchr3:156271443chr8:27455767ENST0000054634379443_447457.6666666666667461.0MotifNuclear localization signal
TgeneCLUchr3:156271443chr8:27455767ENST000005463437978_81457.6666666666667461.0MotifNuclear localization signal
TgeneCLUchr3:156271443chr8:27455767ENST0000056036679443_447498.6666666666667502.0MotifNuclear localization signal
TgeneCLUchr3:156271443chr8:27455767ENST000005603667978_81498.6666666666667502.0MotifNuclear localization signal


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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
SSR3
CLUall 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


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Related Drugs to SSR3-CLU


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 SSR3-CLU


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
TgeneCLUC0022660Kidney Failure, Acute6CTD_human
TgeneCLUC1565662Acute Kidney Insufficiency6CTD_human
TgeneCLUC2609414Acute kidney injury6CTD_human
TgeneCLUC0002395Alzheimer's Disease3CTD_human
TgeneCLUC0011265Presenile dementia3CTD_human
TgeneCLUC0022658Kidney Diseases3CTD_human
TgeneCLUC0276496Familial Alzheimer Disease (FAD)3CTD_human
TgeneCLUC0494463Alzheimer Disease, Late Onset3CTD_human
TgeneCLUC0546126Acute Confusional Senile Dementia3CTD_human
TgeneCLUC0750900Alzheimer's Disease, Focal Onset3CTD_human
TgeneCLUC0750901Alzheimer Disease, Early Onset3CTD_human
TgeneCLUC0013221Drug toxicity2CTD_human
TgeneCLUC0029408Degenerative polyarthritis2CTD_human
TgeneCLUC0041755Adverse reaction to drug2CTD_human
TgeneCLUC0086743Osteoarthrosis Deformans2CTD_human
TgeneCLUC0019193Hepatitis, Toxic1CTD_human
TgeneCLUC0022333Jacksonian Seizure1CTD_human
TgeneCLUC0024141Lupus Erythematosus, Systemic1CTD_human
TgeneCLUC0025202melanoma1CTD_human
TgeneCLUC0027686Pathologic Neovascularization1CTD_human
TgeneCLUC0033578Prostatic Neoplasms1CTD_human
TgeneCLUC0036341Schizophrenia1PSYGENET
TgeneCLUC0036572Seizures1CTD_human
TgeneCLUC0087031Juvenile-Onset Still Disease1CTD_human
TgeneCLUC0149958Complex partial seizures1CTD_human
TgeneCLUC0234533Generalized seizures1CTD_human
TgeneCLUC0234535Clonic Seizures1CTD_human
TgeneCLUC0234985Mental deterioration1CTD_human
TgeneCLUC0242380Libman-Sacks Disease1CTD_human
TgeneCLUC0270824Visual seizure1CTD_human
TgeneCLUC0270844Tonic Seizures1CTD_human
TgeneCLUC0270846Epileptic drop attack1CTD_human
TgeneCLUC0333641Atrophic1CTD_human
TgeneCLUC0338656Impaired cognition1CTD_human
TgeneCLUC0376358Malignant neoplasm of prostate1CTD_human
TgeneCLUC0422850Seizures, Somatosensory1CTD_human
TgeneCLUC0422852Seizures, Auditory1CTD_human
TgeneCLUC0422853Olfactory seizure1CTD_human
TgeneCLUC0422854Gustatory seizure1CTD_human
TgeneCLUC0422855Vertiginous seizure1CTD_human
TgeneCLUC0494475Tonic - clonic seizures1CTD_human
TgeneCLUC0751056Non-epileptic convulsion1CTD_human
TgeneCLUC0751110Single Seizure1CTD_human
TgeneCLUC0751123Atonic Absence Seizures1CTD_human
TgeneCLUC0751494Convulsive Seizures1CTD_human
TgeneCLUC0751495Seizures, Focal1CTD_human
TgeneCLUC0751496Seizures, Sensory1CTD_human
TgeneCLUC0860207Drug-Induced Liver Disease1CTD_human
TgeneCLUC1262760Hepatitis, Drug-Induced1CTD_human
TgeneCLUC1270972Mild cognitive disorder1CTD_human
TgeneCLUC1862939AMYOTROPHIC LATERAL SCLEROSIS 11CTD_human
TgeneCLUC1862941Amyotrophic Lateral Sclerosis, Sporadic1CTD_human
TgeneCLUC3495559Juvenile arthritis1CTD_human
TgeneCLUC3495874Nonepileptic Seizures1CTD_human
TgeneCLUC3658290Drug-Induced Acute Liver Injury1CTD_human
TgeneCLUC3714758Juvenile psoriatic arthritis1CTD_human
TgeneCLUC4048158Convulsions1CTD_human
TgeneCLUC4277682Chemical and Drug Induced Liver Injury1CTD_human
TgeneCLUC4279912Chemically-Induced Liver Toxicity1CTD_human
TgeneCLUC4316903Absence Seizures1CTD_human
TgeneCLUC4317109Epileptic Seizures1CTD_human
TgeneCLUC4317123Myoclonic Seizures1CTD_human
TgeneCLUC4505436Generalized Absence Seizures1CTD_human
TgeneCLUC4551993Amyotrophic Lateral Sclerosis, Familial1CTD_human
TgeneCLUC4552091Polyarthritis, Juvenile, Rheumatoid Factor Negative1CTD_human
TgeneCLUC4704862Polyarthritis, Juvenile, Rheumatoid Factor Positive1CTD_human