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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: 32390

FusionGeneSummary for RUNX1T1_TANC2

check button Fusion gene summary
Fusion gene informationFusion gene name: RUNX1T1_TANC2
Fusion gene ID: 32390
HgeneTgene
Gene symbol

RUNX1T1

TANC2

Gene ID

862

26115

Gene nameRUNX1 translocation partner 1tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2
SynonymsAML1-MTG8|AML1T1|CBFA2T1|CDR|ETO|MTG8|ZMYND2ROLSA|rols
Cytomap

8q21.3

17q23.2-q23.3

Type of geneprotein-codingprotein-coding
Descriptionprotein CBFA2T1acute myelogenous leukemia 1 translocation 1, cyclin-D relatedcore-binding factor, runt domain, alpha subunit 2; translocated to, 1; cyclin D-relatedeight twenty one proteinmyeloid translocation gene on 8q22runt related transcription fprotein TANC2putative ankyrin-repeat containing proteinrolling pebbles homolog Btetratricopeptide repeat, ankyrin repeat and coiled-coil domain-containing protein 2
Modification date2018052320180519
UniProtAcc

Q06455

Q9HCD6

Ensembl transtripts involved in fusion geneENST00000523629, ENST00000396218, 
ENST00000265814, ENST00000360348, 
ENST00000436581, ENST00000520724, 
ENST00000518844, ENST00000522163, 
ENST00000422361, ENST00000521553, 
ENST00000424789, ENST00000389520, 
Fusion gene scores* DoF score10 X 12 X 5=60014 X 11 X 5=770
# samples 1213
** MAII scorelog2(12/600*10)=-2.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/770*10)=-2.56634682255381
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RUNX1T1 [Title/Abstract] AND TANC2 [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
HgeneRUNX1T1

GO:0045892

negative regulation of transcription, DNA-templated

23251453


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
ChiTaRS3.1DQ202695RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
* 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-intronENST00000523629ENST00000424789RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000523629ENST00000389520RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000396218ENST00000424789RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000396218ENST00000389520RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000265814ENST00000424789RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000265814ENST00000389520RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000360348ENST00000424789RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000360348ENST00000389520RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000436581ENST00000424789RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000436581ENST00000389520RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000520724ENST00000424789RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000520724ENST00000389520RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000518844ENST00000424789RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000518844ENST00000389520RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000522163ENST00000424789RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000522163ENST00000389520RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000422361ENST00000424789RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000422361ENST00000389520RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000521553ENST00000424789RUNX1T1chr8

93078576

-TANC2chr17

61226151

+
intron-intronENST00000521553ENST00000389520RUNX1T1chr8

93078576

-TANC2chr17

61226151

+

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FusionProtFeatures for RUNX1T1_TANC2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RUNX1T1

Q06455

TANC2

Q9HCD6


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 RUNX1T1_TANC2


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 RUNX1T1_TANC2


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 RUNX1T1_TANC2


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 RUNX1T1_TANC2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRUNX1T1C0023467Leukemia, Myelocytic, Acute2CTD_human
HgeneRUNX1T1C0149925Small cell carcinoma of lung1CTD_human