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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: 16072

FusionGeneSummary for HELZ_C7orf25

check button Fusion gene summary
Fusion gene informationFusion gene name: HELZ_C7orf25
Fusion gene ID: 16072
HgeneTgene
Gene symbol

HELZ

C7orf25

Gene ID

9931

79020

Gene namehelicase with zinc fingerchromosome 7 open reading frame 25
SynonymsDHRC|DRHC|HUMORF5-
Cytomap

17q24.2

7p14.1

Type of geneprotein-codingprotein-coding
Descriptionprobable helicase with zinc finger domaindown-regulated in human cancers proteinhelicase with zinc finger domainUPF0415 protein C7orf25
Modification date2018052620180519
UniProtAcc

P42694

Q9BPX7

Ensembl transtripts involved in fusion geneENST00000358691, ENST00000580168, 
ENST00000580662, 
ENST00000350427, 
ENST00000447342, ENST00000431882, 
ENST00000438029, 
Fusion gene scores* DoF score17 X 16 X 7=19042 X 2 X 1=4
# samples 172
** MAII scorelog2(17/1904*10)=-3.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: HELZ [Title/Abstract] AND C7orf25 [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

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
ChiTaRS3.1BG291710HELZchr17

65070293

-C7orf25chr7

42949277

-
* 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
intron-3CDSENST00000358691ENST00000350427HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000358691ENST00000447342HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000358691ENST00000431882HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000358691ENST00000438029HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000580168ENST00000350427HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000580168ENST00000447342HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000580168ENST00000431882HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000580168ENST00000438029HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000580662ENST00000350427HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000580662ENST00000447342HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000580662ENST00000431882HELZchr17

65070293

-C7orf25chr7

42949277

-
intron-3CDSENST00000580662ENST00000438029HELZchr17

65070293

-C7orf25chr7

42949277

-

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FusionProtFeatures for HELZ_C7orf25


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

P42694

C7orf25

Q9BPX7

May act as a helicase that plays a role in RNAmetabolism in multiple tissues and organs within the developingembryo.

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 HELZ_C7orf25


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 HELZ_C7orf25


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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RelatedDrugs for HELZ_C7orf25


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 HELZ_C7orf25


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource