FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 10180

FusionGeneSummary for DNAH14_EPHX1

check button Fusion gene summary
Fusion gene informationFusion gene name: DNAH14_EPHX1
Fusion gene ID: 10180
HgeneTgene
Gene symbol

DNAH14

EPHX1

Gene ID

127602

2052

Gene namedynein axonemal heavy chain 14epoxide hydrolase 1
SynonymsC1orf67|Dnahc14|HL-18|HL18EPHX|EPOX|HYL1|MEH
Cytomap

1q42.12

1q42.12

Type of geneprotein-codingprotein-coding
Descriptiondynein heavy chain 14, axonemalaxonemal beta dynein heavy chain 14ciliary dynein heavy chain 14dynein, axonemal, heavy polypeptide 14epoxide hydrolase 1epoxide hydrataseepoxide hydrolase 1 microsomalepoxide hydrolase 1, microsomal (xenobiotic)
Modification date2018052320180519
UniProtAcc

Q0VDD8

P07099

Ensembl transtripts involved in fusion geneENST00000445597, ENST00000430092, 
ENST00000439375, ENST00000400952, 
ENST00000366849, ENST00000366850, 
ENST00000498360, ENST00000366848, 
ENST00000272167, ENST00000366837, 
ENST00000467015, 
Fusion gene scores* DoF score4 X 3 X 4=488 X 6 X 5=240
# samples 412
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/240*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DNAH14 [Title/Abstract] AND EPHX1 [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
TgeneEPHX1

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
TCGALDLUADTCGA-J2-A4AD-01ADNAH14chr1

225117537

+EPHX1chr1

226016426

+
* 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
5CDS-5UTRENST00000445597ENST00000272167DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5CDS-5UTRENST00000445597ENST00000366837DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5CDS-intronENST00000445597ENST00000467015DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-5UTRENST00000430092ENST00000272167DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-5UTRENST00000430092ENST00000366837DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-intronENST00000430092ENST00000467015DNAH14chr1

225117537

+EPHX1chr1

226016426

+
intron-5UTRENST00000439375ENST00000272167DNAH14chr1

225117537

+EPHX1chr1

226016426

+
intron-5UTRENST00000439375ENST00000366837DNAH14chr1

225117537

+EPHX1chr1

226016426

+
intron-intronENST00000439375ENST00000467015DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-5UTRENST00000400952ENST00000272167DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-5UTRENST00000400952ENST00000366837DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-intronENST00000400952ENST00000467015DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-5UTRENST00000366849ENST00000272167DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-5UTRENST00000366849ENST00000366837DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-intronENST00000366849ENST00000467015DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-5UTRENST00000366850ENST00000272167DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-5UTRENST00000366850ENST00000366837DNAH14chr1

225117537

+EPHX1chr1

226016426

+
5UTR-intronENST00000366850ENST00000467015DNAH14chr1

225117537

+EPHX1chr1

226016426

+
3UTR-5UTRENST00000498360ENST00000272167DNAH14chr1

225117537

+EPHX1chr1

226016426

+
3UTR-5UTRENST00000498360ENST00000366837DNAH14chr1

225117537

+EPHX1chr1

226016426

+
3UTR-intronENST00000498360ENST00000467015DNAH14chr1

225117537

+EPHX1chr1

226016426

+
intron-5UTRENST00000366848ENST00000272167DNAH14chr1

225117537

+EPHX1chr1

226016426

+
intron-5UTRENST00000366848ENST00000366837DNAH14chr1

225117537

+EPHX1chr1

226016426

+
intron-intronENST00000366848ENST00000467015DNAH14chr1

225117537

+EPHX1chr1

226016426

+

Top

FusionProtFeatures for DNAH14_EPHX1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DNAH14

Q0VDD8

EPHX1

P07099


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


Top

FusionGeneSequence for DNAH14_EPHX1


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).

Top

FusionGenePPI for DNAH14_EPHX1


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
DNAH14APP, IGSF8, DLK1, CETN2, CAMK2D, SSSCA1, IKZF5, CETN1, RELL2, GFAPEPHX1DNAJB11, 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, NMUR2


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


Top

RelatedDrugs for DNAH14_EPHX1


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

Top

RelatedDiseases for DNAH14_EPHX1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneEPHX1C0033578Prostatic Neoplasms3CTD_human
TgeneEPHX1C0024121Lung Neoplasms2CTD_human
TgeneEPHX1C0032914Pre-Eclampsia2CTD_human
TgeneEPHX1C0001973Alcoholic Intoxication, Chronic1PSYGENET
TgeneEPHX1C0024117Chronic Obstructive Airway Disease1CTD_human
TgeneEPHX1C0024299Lymphoma1CTD_human
TgeneEPHX1C0024305Lymphoma, Non-Hodgkin1CTD_human
TgeneEPHX1C0024667Animal Mammary Neoplasms1CTD_human
TgeneEPHX1C0024668Mammary Neoplasms, Experimental1CTD_human
TgeneEPHX1C0026764Multiple Myeloma1CTD_human
TgeneEPHX1C0034067Pulmonary Emphysema1CTD_human
TgeneEPHX1C0037286Skin Neoplasms1CTD_human
TgeneEPHX1C0236733Amphetamine-Related Disorders1CTD_human
TgeneEPHX1C0345967Malignant mesothelioma1CTD_human
TgeneEPHX1C1449861Micronuclei, Chromosome-Defective1CTD_human
TgeneEPHX1C1961102Precursor Cell Lymphoblastic Leukemia Lymphoma1CTD_human
TgeneEPHX1C2239176Liver carcinoma1CTD_human
TgeneEPHX1C4277682Chemical and Drug Induced Liver Injury1CTD_human