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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:GPX4-SEC63 (FusionGDB2 ID:34439)

Fusion Gene Summary for GPX4-SEC63

check button Fusion gene summary
Fusion gene informationFusion gene name: GPX4-SEC63
Fusion gene ID: 34439
HgeneTgene
Gene symbol

GPX4

SEC63

Gene ID

2879

11231

Gene nameglutathione peroxidase 4SEC63 homolog, protein translocation regulator
SynonymsGPx-4|GSHPx-4|MCSP|PHGPx|SMDS|snGPx|snPHGPxDNAJC23|ERdj2|PCLD2|PRO2507|SEC63L
Cytomap

19p13.3

6q21

Type of geneprotein-codingprotein-coding
Descriptionphospholipid hydroperoxide glutathione peroxidaseepididymis secretory sperm binding proteinphospholipid hydroperoxidasephospholipid hydroperoxide glutathione peroxidase, mitochondrialsperm nucleus glutathione peroxidasetranslocation protein SEC63 homologSEC63 protein translocation regulatorSEC63-like protein
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000354171, ENST00000589115, 
ENST00000369002, ENST00000460009, 
Fusion gene scores* DoF score9 X 7 X 5=31538 X 14 X 15=7980
# samples 1039
** MAII scorelog2(10/315*10)=-1.65535182861255
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(39/7980*10)=-4.3548427173601
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GPX4 [Title/Abstract] AND SEC63 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGPX4(1106786)-SEC63(108214782), # samples:1
Anticipated loss of major functional domain due to fusion event.GPX4-SEC63 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
GPX4-SEC63 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
GPX4-SEC63 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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

check buttonFusion gene breakpoints across GPX4 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across SEC63 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4THCATCGA-EM-A22K-01AGPX4chr19

1106786

-SEC63chr6

108214782

-


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Fusion Gene ORF analysis for GPX4-SEC63

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
intron-3CDSENST00000354171ENST00000369002GPX4chr19

1106786

-SEC63chr6

108214782

-
intron-intronENST00000354171ENST00000460009GPX4chr19

1106786

-SEC63chr6

108214782

-
Frame-shiftENST00000589115ENST00000369002GPX4chr19

1106786

-SEC63chr6

108214782

-
5CDS-intronENST00000589115ENST00000460009GPX4chr19

1106786

-SEC63chr6

108214782

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

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

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Fusion Genomic Features for GPX4-SEC63


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for GPX4-SEC63


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
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: 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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for GPX4-SEC63


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for GPX4-SEC63


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 (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for GPX4-SEC63


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for GPX4-SEC63


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGPX4C0021364Male infertility2CTD_human
HgeneGPX4C0848676Subfertility, Male2CTD_human
HgeneGPX4C0917731Male sterility2CTD_human
HgeneGPX4C0006142Malignant neoplasm of breast1CTD_human
HgeneGPX4C0006635Cadmium poisoning1CTD_human
HgeneGPX4C0009402Colorectal Carcinoma1CTD_human
HgeneGPX4C0009404Colorectal Neoplasms1CTD_human
HgeneGPX4C0010417Cryptorchidism1CTD_human
HgeneGPX4C0012684Blastocyst Disintegration1CTD_human
HgeneGPX4C0013937Embryo Resorption1CTD_human
HgeneGPX4C0015695Fatty Liver1CTD_human
HgeneGPX4C0016059Fibrosis1CTD_human
HgeneGPX4C0018801Heart failure1CTD_human
HgeneGPX4C0018802Congestive heart failure1CTD_human
HgeneGPX4C0023212Left-Sided Heart Failure1CTD_human
HgeneGPX4C0235527Heart Failure, Right-Sided1CTD_human
HgeneGPX4C0271650Impaired glucose tolerance1CTD_human
HgeneGPX4C0431663Bilateral Cryptorchidism1CTD_human
HgeneGPX4C0431664Unilateral Cryptorchidism1CTD_human
HgeneGPX4C0678222Breast Carcinoma1CTD_human
HgeneGPX4C0752350Embryo Death1CTD_human
HgeneGPX4C0752351Embryo Loss1CTD_human
HgeneGPX4C1136082Embryo Disintegration1CTD_human
HgeneGPX4C1257931Mammary Neoplasms, Human1CTD_human
HgeneGPX4C1458155Mammary Neoplasms1CTD_human
HgeneGPX4C1563730Abdominal Cryptorchidism1CTD_human
HgeneGPX4C1563731Inguinal Cryptorchidism1CTD_human
HgeneGPX4C1623038Cirrhosis1CTD_human
HgeneGPX4C1855229Spondylometaphyseal dysplasia, Sedaghatian type1CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneGPX4C1959583Myocardial Failure1CTD_human
HgeneGPX4C1961112Heart Decompensation1CTD_human
HgeneGPX4C2711227Steatohepatitis1CTD_human
HgeneGPX4C4704874Mammary Carcinoma, Human1CTD_human
TgeneSEC63C0158683Polycystic liver disease2CTD_human;ORPHANET
TgeneSEC63C0022680Polycystic Kidney Diseases1CTD_human
TgeneSEC63C1567435Polycystic Kidney - body part1CTD_human
TgeneSEC63C4310769POLYCYSTIC LIVER DISEASE 2 WITH OR WITHOUT KIDNEY CYSTS1GENOMICS_ENGLAND