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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: 10014

FusionGeneSummary for DIP2C_ORC4

check button Fusion gene summary
Fusion gene informationFusion gene name: DIP2C_ORC4
Fusion gene ID: 10014
HgeneTgene
Gene symbol

DIP2C

ORC4

Gene ID

22982

5000

Gene namedisco interacting protein 2 homolog Corigin recognition complex subunit 4
SynonymsKIAA0934ORC4L|ORC4P
Cytomap

10p15.3

2q23.1

Type of geneprotein-codingprotein-coding
Descriptiondisco-interacting protein 2 homolog CDIP2 disco-interacting protein 2 homolog CDIP2 homolog Corigin recognition complex subunit 4origin recognition complex, subunit 4 homolog
Modification date2018051920180523
UniProtAcc

Q9Y2E4

O43929

Ensembl transtripts involved in fusion geneENST00000280886, ENST00000381496, 
ENST00000540204, 
ENST00000392857, 
ENST00000392858, ENST00000535373, 
ENST00000536575, ENST00000540442, 
ENST00000264169, ENST00000542387, 
ENST00000488761, 
Fusion gene scores* DoF score13 X 7 X 11=10014 X 4 X 3=48
# samples 144
** MAII scorelog2(14/1001*10)=-2.83794324189103
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DIP2C [Title/Abstract] AND ORC4 [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
TCGALDSARCTCGA-K1-A6RV-01ADIP2Cchr10

735434

-ORC4chr2

148733544

-
* 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-5UTRENST00000280886ENST00000392857DIP2Cchr10

735434

-ORC4chr2

148733544

-
5CDS-5UTRENST00000280886ENST00000392858DIP2Cchr10

735434

-ORC4chr2

148733544

-
5CDS-5UTRENST00000280886ENST00000535373DIP2Cchr10

735434

-ORC4chr2

148733544

-
5CDS-intronENST00000280886ENST00000536575DIP2Cchr10

735434

-ORC4chr2

148733544

-
5CDS-intronENST00000280886ENST00000540442DIP2Cchr10

735434

-ORC4chr2

148733544

-
5CDS-5UTRENST00000280886ENST00000264169DIP2Cchr10

735434

-ORC4chr2

148733544

-
5CDS-5UTRENST00000280886ENST00000542387DIP2Cchr10

735434

-ORC4chr2

148733544

-
5CDS-intronENST00000280886ENST00000488761DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-5UTRENST00000381496ENST00000392857DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-5UTRENST00000381496ENST00000392858DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-5UTRENST00000381496ENST00000535373DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-intronENST00000381496ENST00000536575DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-intronENST00000381496ENST00000540442DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-5UTRENST00000381496ENST00000264169DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-5UTRENST00000381496ENST00000542387DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-intronENST00000381496ENST00000488761DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-5UTRENST00000540204ENST00000392857DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-5UTRENST00000540204ENST00000392858DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-5UTRENST00000540204ENST00000535373DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-intronENST00000540204ENST00000536575DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-intronENST00000540204ENST00000540442DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-5UTRENST00000540204ENST00000264169DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-5UTRENST00000540204ENST00000542387DIP2Cchr10

735434

-ORC4chr2

148733544

-
intron-intronENST00000540204ENST00000488761DIP2Cchr10

735434

-ORC4chr2

148733544

-

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FusionProtFeatures for DIP2C_ORC4


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DIP2C

Q9Y2E4

ORC4

O43929

Component of the origin recognition complex (ORC) thatbinds origins of replication. DNA-binding is ATP-dependent. Thespecific DNA sequences that define origins of replication have notbeen identified yet. ORC is required to assemble the pre-replication complex necessary to initiate DNA replication. Bindshistone H3 and H4 trimethylation marks H3K9me3, H3K27me3 andH4K20me3. {ECO:0000269|PubMed:22427655}.

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 DIP2C_ORC4


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 DIP2C_ORC4


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
DIP2CPCBD1, PIP4K2A, TRIM25ORC4MCM2, MCM3, ORC1, ORC2, ORC5, ORC6, MCM4, MCM6, RPA2, DBF4, ORC3, CCL2, XRCC5, XRCC6, APP, MCM7, MCM10, CCND1, CDKN2A, FBXO6, CTBP1, KPNA1, MLH1, FBXL5, FBXO25, FBXL8, MTUS1, TCF4, RRM2B, HIST3H3, HIST4H4, LACC1, PABPC1, CAPZA2, TSNAX, KLC3, LRWD1, TEAD2, FOXL1, SNW1, CDC5L, MTMR3, CD93, LAMP1, DLK1, IL1R2, TXNDC15, P2RX4


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 DIP2C_ORC4


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 DIP2C_ORC4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDIP2CC0149925Small cell carcinoma of lung1CTD_human
TgeneORC4C1868684EAR, PATELLA, SHORT STATURE SYNDROME2CTD_human;ORPHANET
TgeneORC4C3151097MEIER-GORLIN SYNDROME 21UNIPROT