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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: 9029

FusionGeneSummary for CUX2_IFT81

check button Fusion gene summary
Fusion gene informationFusion gene name: CUX2_IFT81
Fusion gene ID: 9029
HgeneTgene
Gene symbol

CUX2

IFT81

Gene ID

23316

28981

Gene namecut like homeobox 2intraflagellar transport 81
SynonymsCDP2|CUTL2CDV-1|CDV-1R|CDV1|CDV1R|DV1|SRTD19
Cytomap

12q24.11-q24.12

12q24.11

Type of geneprotein-codingprotein-coding
Descriptionhomeobox protein cut-like 2homeobox protein cux-2intraflagellar transport protein 81 homologcarnitine deficiency-associated gene expressed in ventricle 1carnitine deficiency-associated protein expressed in ventricle 1
Modification date2018052320180523
UniProtAcc

O14529

Q8WYA0

Ensembl transtripts involved in fusion geneENST00000261726, ENST00000551604, 
ENST00000552912, ENST00000242591, 
ENST00000361948, ENST00000549009, 
Fusion gene scores* DoF score5 X 4 X 3=605 X 6 X 7=210
# samples 58
** MAII scorelog2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/210*10)=-1.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CUX2 [Title/Abstract] AND IFT81 [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
HgeneCUX2

GO:0000122

negative regulation of transcription by RNA polymerase II

15656993


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
TCGARVUCSTCGA-NA-A4R1-01ACUX2chr12

111472044

+IFT81chr12

110565165

+
* 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-5UTRENST00000261726ENST00000552912CUX2chr12

111472044

+IFT81chr12

110565165

+
5CDS-5UTRENST00000261726ENST00000242591CUX2chr12

111472044

+IFT81chr12

110565165

+
5CDS-5UTRENST00000261726ENST00000361948CUX2chr12

111472044

+IFT81chr12

110565165

+
5CDS-intronENST00000261726ENST00000549009CUX2chr12

111472044

+IFT81chr12

110565165

+
intron-5UTRENST00000551604ENST00000552912CUX2chr12

111472044

+IFT81chr12

110565165

+
intron-5UTRENST00000551604ENST00000242591CUX2chr12

111472044

+IFT81chr12

110565165

+
intron-5UTRENST00000551604ENST00000361948CUX2chr12

111472044

+IFT81chr12

110565165

+
intron-intronENST00000551604ENST00000549009CUX2chr12

111472044

+IFT81chr12

110565165

+

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FusionProtFeatures for CUX2_IFT81


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CUX2

O14529

IFT81

Q8WYA0

May be a transcription factor involved in neuralspecification. Binds to DNA in a sequence-specific manner (Bysimilarity). {ECO:0000250}. Component of the intraflagellar transport (IFT) complexB: together with IFT74, forms a tubulin-binding module thatspecifically mediates transport of tubulin within the cilium.Binds tubulin via its CH (calponin-homology)-like region(PubMed:23990561). Required for ciliogenesis (PubMed:27666822,PubMed:23990561). Required for proper regulation of SHH signaling(PubMed:27666822). {ECO:0000269|PubMed:23990561,ECO:0000269|PubMed:27666822}.

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 CUX2_IFT81


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 CUX2_IFT81


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
CUX2IFT81APP, IFT88, IFT57, CCDC151, ARL13B, IFT46, PRAME, IFT74, SPATA5L1, NDC80, CEP44, PCM1, LTBR, NTRK1, MED4, LCA5, OFD1, CEP128, CEP63, CNTRL, FBF1, NINL, ODF2, GLI1, UBXN10, TTC30A, TTC30B, JPH4, FGF8, RHPN1, SERPINB2, CORO6, HSPB11, IFT52, IFT27, IFT22, IFT172, TTC26, CCDC28B, IFT20, IFT80


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 CUX2_IFT81


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 CUX2_IFT81


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCUX2C0005586Bipolar Disorder1PSYGENET
HgeneCUX2C1839839MAJOR AFFECTIVE DISORDER 21PSYGENET