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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 11830

FusionGeneSummary for EPHX1_SEC63

check button Fusion gene summary
Fusion gene informationFusion gene name: EPHX1_SEC63
Fusion gene ID: 11830
HgeneTgene
Gene symbol

EPHX1

SEC63

Gene ID

2052

11231

Gene nameepoxide hydrolase 1SEC63 homolog, protein translocation regulator
SynonymsEPHX|EPOX|HYL1|MEHDNAJC23|ERdj2|PCLD2|PRO2507|SEC63L
Cytomap

1q42.12

6q21

Type of geneprotein-codingprotein-coding
Descriptionepoxide hydrolase 1epoxide hydrataseepoxide hydrolase 1 microsomalepoxide hydrolase 1, microsomal (xenobiotic)translocation protein SEC63 homologSEC63 protein translocation regulatorSEC63-like protein
Modification date2018051920180523
UniProtAcc

P07099

Q9UGP8

Ensembl transtripts involved in fusion geneENST00000272167, ENST00000366837, 
ENST00000467015, 
ENST00000369002, 
ENST00000460009, 
Fusion gene scores* DoF score3 X 3 X 2=1830 X 6 X 14=2520
# samples 333
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(33/2520*10)=-2.93288580414146
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: EPHX1 [Title/Abstract] AND SEC63 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgeneEPHX1

GO:0097176

epoxide metabolic process

22798687


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGARVLIHCTCGA-CC-A7IL-01AEPHX1chr1

226033260

+SEC63chr6

108214782

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
Frame-shiftENST00000272167ENST00000369002EPHX1chr1

226033260

+SEC63chr6

108214782

-
5CDS-intronENST00000272167ENST00000460009EPHX1chr1

226033260

+SEC63chr6

108214782

-
Frame-shiftENST00000366837ENST00000369002EPHX1chr1

226033260

+SEC63chr6

108214782

-
5CDS-intronENST00000366837ENST00000460009EPHX1chr1

226033260

+SEC63chr6

108214782

-
intron-3CDSENST00000467015ENST00000369002EPHX1chr1

226033260

+SEC63chr6

108214782

-
intron-intronENST00000467015ENST00000460009EPHX1chr1

226033260

+SEC63chr6

108214782

-

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FusionProtFeatures for EPHX1_SEC63


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
EPHX1

P07099

SEC63

Q9UGP8

Required for integral membrane and secreted preproteintranslocation across the endoplasmic reticulum membrane.

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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FusionGeneSequence for EPHX1_SEC63


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for EPHX1_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
EPHX1DNAJB11, CDKN2AIP, HPDL, ATP4A, NXF1, RNF2, DERL1, SPINT2, SRPRB, TMEM30A, TSPAN17, TREML2, FAM189A2, PTGER3, EVA1C, IQCF1, CHRNA9, CKMT1A, CKMT1B, HADHA, TMED10, TMX1, RAB34, MFSD8, KCNS3, TRAF1, PCDHGB4, PCDHGA5, NMUR2SEC63GSTK1, IRF1, PMF1, SPA17, GPR183, RFX3, GPRC5D, SKAP1, ACADM, RPS5, ABCC1, DDOST, KPNA4, SEC61A1, NTRK1, TP53, OFD1, TCTN2, TCTN3, NPHP1, RPGRIP1L, EVC2, TCTN1, TMEM17, TMEM216, HSPA5, SENP3, CDKN3, YIPF3, HTR2C, ARFGAP1, BIN3, GPRC5B, TPTE, NR3C1, TRIM25


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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RelatedDrugs for EPHX1_SEC63


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for EPHX1_SEC63


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneEPHX1C0033578Prostatic Neoplasms3CTD_human
HgeneEPHX1C0024121Lung Neoplasms2CTD_human
HgeneEPHX1C0032914Pre-Eclampsia2CTD_human
HgeneEPHX1C0001973Alcoholic Intoxication, Chronic1PSYGENET
HgeneEPHX1C0024117Chronic Obstructive Airway Disease1CTD_human
HgeneEPHX1C0024299Lymphoma1CTD_human
HgeneEPHX1C0024305Lymphoma, Non-Hodgkin1CTD_human
HgeneEPHX1C0024667Animal Mammary Neoplasms1CTD_human
HgeneEPHX1C0024668Mammary Neoplasms, Experimental1CTD_human
HgeneEPHX1C0026764Multiple Myeloma1CTD_human
HgeneEPHX1C0034067Pulmonary Emphysema1CTD_human
HgeneEPHX1C0037286Skin Neoplasms1CTD_human
HgeneEPHX1C0236733Amphetamine-Related Disorders1CTD_human
HgeneEPHX1C0345967Malignant mesothelioma1CTD_human
HgeneEPHX1C1449861Micronuclei, Chromosome-Defective1CTD_human
HgeneEPHX1C1961102Precursor Cell Lymphoblastic Leukemia Lymphoma1CTD_human
HgeneEPHX1C2239176Liver carcinoma1CTD_human
HgeneEPHX1C4277682Chemical and Drug Induced Liver Injury1CTD_human
TgeneSEC63C0022680Polycystic Kidney Diseases1CTD_human
TgeneSEC63C0158683Polycystic liver disease1CTD_human;HPO;ORPHANET