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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: 17123

FusionGeneSummary for IFT80_TP73

check button Fusion gene summary
Fusion gene informationFusion gene name: IFT80_TP73
Fusion gene ID: 17123
HgeneTgene
Gene symbol

IFT80

TP73

Gene ID

57560

7161

Gene nameintraflagellar transport 80tumor protein p73
SynonymsATD2|SRTD2|WDR56P73
Cytomap

3q25.33

1p36.32

Type of geneprotein-codingprotein-coding
Descriptionintraflagellar transport protein 80 homologWD repeat domain 56WD repeat-containing protein 56intraflagellar transport 80 homologtumor protein p73p53-like transcription factorp53-related protein
Modification date2018052320180522
UniProtAcc

Q9P2H3

O15350

Ensembl transtripts involved in fusion geneENST00000326448, ENST00000483465, 
ENST00000496589, ENST00000477495, 
ENST00000378295, ENST00000604074, 
ENST00000354437, ENST00000346387, 
ENST00000357733, ENST00000603362, 
ENST00000604479, ENST00000378285, 
ENST00000378280, ENST00000378288, 
ENST00000378290, 
Fusion gene scores* DoF score6 X 6 X 4=1442 X 2 X 2=8
# samples 83
** MAII scorelog2(8/144*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/8*10)=1.90689059560852
Context

PubMed: IFT80 [Title/Abstract] AND TP73 [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
TgeneTP73

GO:0006974

cellular response to DNA damage stimulus

18174154

TgeneTP73

GO:0042771

intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator

18174154|19490146

TgeneTP73

GO:0045893

positive regulation of transcription, DNA-templated

15678106|16343436

TgeneTP73

GO:0045944

positive regulation of transcription by RNA polymerase II

16343436|18174154|18421303|19490146|24652652

TgeneTP73

GO:0071158

positive regulation of cell cycle arrest

18421303


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
ChiTaRS3.1CR740291IFT80chr3

160126797

+TP73chr1

3580033

-
ChiTaRS3.1BX280087IFT80chr3

160126797

+TP73chr1

3580033

-
* 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-intronENST00000326448ENST00000378295IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000326448ENST00000604074IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000326448ENST00000354437IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000326448ENST00000346387IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000326448ENST00000357733IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000326448ENST00000603362IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000326448ENST00000604479IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000326448ENST00000378285IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000326448ENST00000378280IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000326448ENST00000378288IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000326448ENST00000378290IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000378295IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000604074IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000354437IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000346387IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000357733IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000603362IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000604479IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000378285IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000378280IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000378288IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000483465ENST00000378290IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000378295IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000604074IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000354437IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000346387IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000357733IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000603362IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000604479IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000378285IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000378280IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000378288IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000496589ENST00000378290IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000378295IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000604074IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000354437IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000346387IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000357733IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000603362IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000604479IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000378285IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000378280IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000378288IFT80chr3

160126797

+TP73chr1

3580033

-
intron-intronENST00000477495ENST00000378290IFT80chr3

160126797

+TP73chr1

3580033

-

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FusionProtFeatures for IFT80_TP73


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
IFT80

Q9P2H3

TP73

O15350

Component of the intraflagellar transport (IFT) complexB, which is essential for the development and maintenance ofmotile and sensory cilia. {ECO:0000269|PubMed:17468754}.

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 IFT80_TP73


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 IFT80_TP73


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 IFT80_TP73


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneTP73O15350DB01593ZincTumor protein p73small moleculeapproved|investigational

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RelatedDiseases for IFT80_TP73


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneIFT80C0004044Asphyxia1CTD_human
HgeneIFT80C0005941Bone Diseases, Developmental1CTD_human
HgeneIFT80C0035229Respiratory Insufficiency1CTD_human
HgeneIFT80C0035304Retinal Degeneration1CTD_human
HgeneIFT80C0039978Thoracic Diseases1CTD_human
HgeneIFT80C0152427Polydactyly1CTD_human
HgeneIFT80C1691228Cystic Kidney Diseases1CTD_human
HgeneIFT80C1970005Asphyxiating Thoracic Dystrophy 21CTD_human;UNIPROT
TgeneTP73C0023493Adult T-Cell Lymphoma/Leukemia1CTD_human
TgeneTP73C0206655Alveolar rhabdomyosarcoma1CTD_human