FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 39705

FusionGeneSummary for TRRAP_TMEM168

check button Fusion gene summary
Fusion gene informationFusion gene name: TRRAP_TMEM168
Fusion gene ID: 39705
HgeneTgene
Gene symbol

TRRAP

TMEM168

Gene ID

8295

64418

Gene nametransformation/transcription domain associated proteintransmembrane protein 168
SynonymsPAF350/400|PAF400|STAF40|TR-AP|Tra1-
Cytomap

7q22.1

7q31.1

Type of geneprotein-codingprotein-coding
Descriptiontransformation/transcription domain-associated protein350/400 kDa PCAF-associated factortra1 homologtransmembrane protein 168
Modification date2018052320180519
UniProtAcc

Q9Y4A5

Q9H0V1

Ensembl transtripts involved in fusion geneENST00000355540, ENST00000359863, 
ENST00000446306, 
ENST00000312814, 
ENST00000454074, ENST00000480969, 
Fusion gene scores* DoF score5 X 5 X 4=1002 X 2 X 2=8
# samples 52
** MAII scorelog2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: TRRAP [Title/Abstract] AND TMEM168 [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
HgeneTRRAP

GO:0016578

histone deubiquitination

18206972

HgeneTRRAP

GO:0043967

histone H4 acetylation

14966270

HgeneTRRAP

GO:0043968

histone H2A acetylation

14966270


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
TCGALDLUADTCGA-78-7154-01ATRRAPchr7

98552927

+TMEM168chr7

112425008

-
* 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-5UTRENST00000355540ENST00000312814TRRAPchr7

98552927

+TMEM168chr7

112425008

-
5CDS-5UTRENST00000355540ENST00000454074TRRAPchr7

98552927

+TMEM168chr7

112425008

-
5CDS-intronENST00000355540ENST00000480969TRRAPchr7

98552927

+TMEM168chr7

112425008

-
5CDS-5UTRENST00000359863ENST00000312814TRRAPchr7

98552927

+TMEM168chr7

112425008

-
5CDS-5UTRENST00000359863ENST00000454074TRRAPchr7

98552927

+TMEM168chr7

112425008

-
5CDS-intronENST00000359863ENST00000480969TRRAPchr7

98552927

+TMEM168chr7

112425008

-
5CDS-5UTRENST00000446306ENST00000312814TRRAPchr7

98552927

+TMEM168chr7

112425008

-
5CDS-5UTRENST00000446306ENST00000454074TRRAPchr7

98552927

+TMEM168chr7

112425008

-
5CDS-intronENST00000446306ENST00000480969TRRAPchr7

98552927

+TMEM168chr7

112425008

-

Top

FusionProtFeatures for TRRAP_TMEM168


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

Q9Y4A5

TMEM168

Q9H0V1

Adapter protein, which is found in various multiproteinchromatin complexes with histone acetyltransferase activity (HAT),which gives a specific tag for epigenetic transcriptionactivation. Component of the NuA4 histone acetyltransferasecomplex which is responsible for acetylation of nucleosomalhistones H4 and H2A. Plays a central role in MYC transcriptionactivation, and also participates in cell transformation by MYC.Required for p53/TP53-, E2F1- and E2F4-mediated transcriptionactivation. Also involved in transcription activation mediated bythe adenovirus E1A, a viral oncoprotein that deregulatestranscription of key genes. Probably acts by linking transcriptionfactors such as E1A, MYC or E2F1 to HAT complexes such as STAGAthereby allowing transcription activation. Probably not requiredin the steps following histone acetylation in processes oftranscription activation. May be required for the mitoticcheckpoint and normal cell cycle progression. Component of a SWR1-like complex that specifically mediates the removal of histoneH2A.Z/H2AFZ from the nucleosome. {ECO:0000269|PubMed:11418595,ECO:0000269|PubMed:12138177, ECO:0000269|PubMed:12660246,ECO:0000269|PubMed:12743606, ECO:0000269|PubMed:14966270,ECO:0000269|PubMed:17967892, ECO:0000269|PubMed:24463511,ECO:0000269|PubMed:9708738}.

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


Top

FusionGeneSequence for TRRAP_TMEM168


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).

Top

FusionGenePPI for TRRAP_TMEM168


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
TRRAPMYC, MAX, KAT2A, E2F1, EP400, KAT2B, RUVBL1, ACTL6A, ING1, TAL1, SUPT3H, TAF9, ATXN7L3, USP22, ATXN7, ENY2, ING3, KAT5, OFD1, CTNNB1, TAF10, TTI1, TELO2, MRGBP, TP53, MED1, MED23, MED26, CDK8, MED12, MED13, MED14, MED15, MED16, MED17, MED24, MED25, E2F4, NPAT, USF1, C14orf169, MORF4L1, MORF4L2, SREBF1, CCDC101, DMAP1, PYGO2, ESR1, SIRT7, H2AFZ, SREBF2, ZNF148, CDKN1A, DCUN1D1, SKP1, CUL1, TCF3, TAF9B, TAF7, TAF4, MRE11A, CDC20, TAF5, TAF6, NPM1, DCP2, SOX3, OBSL1, EED, PLAC1, FOXR1, FOXR2, TADA1, TADA2B, TADA3, HIST1H2BA, YEATS4, USP7, BTAF1, VPS72, NCBP1, NCK1, MPHOSPH8, SUPT7L, RUVBL2, BRD8, EPC2, SUPT20H, TTI2, EPC1, KRT72, JAZF1, BRINP1, GAN, FOXO3, SENP3, NFATC1, NFATC2, MBTD1, AURKA, ATOH1, MYCL, MEAF6, SCN3B, STAT2, TAF6L, CACNG5, CREB3L1, HDAC6TMEM168SPP1, CRKL, NETO2, FAM174A, ATP2B2


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


Top

RelatedDrugs for TRRAP_TMEM168


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

Top

RelatedDiseases for TRRAP_TMEM168


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTRRAPC0036341Schizophrenia2CTD_human
HgeneTRRAPC0025202melanoma1CTD_human