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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: 4572

FusionGeneSummary for BTRC_ACIN1

check button Fusion gene summary
Fusion gene informationFusion gene name: BTRC_ACIN1
Fusion gene ID: 4572
HgeneTgene
Gene symbol

BTRC

ACIN1

Gene ID

8945

22985

Gene namebeta-transducin repeat containing E3 ubiquitin protein ligaseapoptotic chromatin condensation inducer 1
SynonymsBETA-TRCP|FBW1A|FBXW1|FBXW1A|FWD1|bTrCP|bTrCP1|betaTrCPACINUS|ACN|fSAP152
Cytomap

10q24.32

14q11.2

Type of geneprotein-codingprotein-coding
DescriptionF-box/WD repeat-containing protein 1AE3RSIkappaBF-box and WD repeats protein beta-TrCPF-box and WD-repeat protein 1Bbeta-TrCP1epididymis tissue protein Li 2apIkappaBalpha-E3 receptor subunitapoptotic chromatin condensation inducer in the nucleusfunctional spliceosome-associated protein 152
Modification date2018052320180522
UniProtAcc

Q9Y297

Q9UKV3

Ensembl transtripts involved in fusion geneENST00000370187, ENST00000393441, 
ENST00000408038, ENST00000493877, 
ENST00000557515, ENST00000338631, 
ENST00000357481, ENST00000605057, 
ENST00000457657, ENST00000262710, 
ENST00000397341, ENST00000555053, 
ENST00000555352, 
Fusion gene scores* DoF score5 X 4 X 5=1007 X 7 X 3=147
# samples 58
** MAII scorelog2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/147*10)=-0.877744249949002
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: BTRC [Title/Abstract] AND ACIN1 [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
HgeneBTRC

GO:0000209

protein polyubiquitination

12820959

HgeneBTRC

GO:0006511

ubiquitin-dependent protein catabolic process

15448698

HgeneBTRC

GO:0016567

protein ubiquitination

16885022

HgeneBTRC

GO:0042752

regulation of circadian rhythm

15917222

HgeneBTRC

GO:0043161

proteasome-mediated ubiquitin-dependent protein catabolic process

15917222

TgeneACIN1

GO:0030263

apoptotic chromosome condensation

10490026


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
ChiTaRS3.1BE819409BTRCchr10

103313525

+ACIN1chr14

23548192

+
* 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
3UTR-intronENST00000370187ENST00000557515BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000370187ENST00000338631BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000370187ENST00000357481BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000370187ENST00000605057BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000370187ENST00000457657BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000370187ENST00000262710BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000370187ENST00000397341BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000370187ENST00000555053BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000370187ENST00000555352BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000393441ENST00000557515BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000393441ENST00000338631BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000393441ENST00000357481BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000393441ENST00000605057BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000393441ENST00000457657BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000393441ENST00000262710BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000393441ENST00000397341BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000393441ENST00000555053BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000393441ENST00000555352BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000408038ENST00000557515BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000408038ENST00000338631BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000408038ENST00000357481BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000408038ENST00000605057BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000408038ENST00000457657BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000408038ENST00000262710BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000408038ENST00000397341BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000408038ENST00000555053BTRCchr10

103313525

+ACIN1chr14

23548192

+
3UTR-intronENST00000408038ENST00000555352BTRCchr10

103313525

+ACIN1chr14

23548192

+
intron-intronENST00000493877ENST00000557515BTRCchr10

103313525

+ACIN1chr14

23548192

+
intron-intronENST00000493877ENST00000338631BTRCchr10

103313525

+ACIN1chr14

23548192

+
intron-intronENST00000493877ENST00000357481BTRCchr10

103313525

+ACIN1chr14

23548192

+
intron-intronENST00000493877ENST00000605057BTRCchr10

103313525

+ACIN1chr14

23548192

+
intron-intronENST00000493877ENST00000457657BTRCchr10

103313525

+ACIN1chr14

23548192

+
intron-intronENST00000493877ENST00000262710BTRCchr10

103313525

+ACIN1chr14

23548192

+
intron-intronENST00000493877ENST00000397341BTRCchr10

103313525

+ACIN1chr14

23548192

+
intron-intronENST00000493877ENST00000555053BTRCchr10

103313525

+ACIN1chr14

23548192

+
intron-intronENST00000493877ENST00000555352BTRCchr10

103313525

+ACIN1chr14

23548192

+

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FusionProtFeatures for BTRC_ACIN1


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

Q9Y297

ACIN1

Q9UKV3

Substrate recognition component of a SCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediatesthe ubiquitination and subsequent proteasomal degradation oftarget proteins. Recognizes and binds to phosphorylated targetproteins (PubMed:10066435, PubMed:10497169, PubMed:10644755,PubMed:10835356, PubMed:11238952, PubMed:11359933,PubMed:11994270, PubMed:12791267, PubMed:12902344,PubMed:14603323, PubMed:14681206, PubMed:14988407,PubMed:15448698, PubMed:15917222, PubMed:16371461,PubMed:25503564, PubMed:25704143, PubMed:9859996). SCF(BTRC)mediates the ubiquitination of CTNNB1 and participates in Wntsignaling (PubMed:12077367, PubMed:12820959). SCF(BTRC) mediatesthe ubiquitination of phosphorylated NFKB1, ATF4, CDC25A, DLG1,FBXO5, PER1, SMAD3, SMAD4, SNAI1 and probably NFKB2(PubMed:10835356, PubMed:11238952, PubMed:14681206,PubMed:14603323). SCF(BTRC) mediates the ubiquitination of NFKBIA,NFKBIB and NFKBIE; the degradation frees the associated NFKB1 totranslocate into the nucleus and to activate transcription(PubMed:10066435, PubMed:10497169, PubMed:10644755).Ubiquitination of NFKBIA occurs at 'Lys-21' and 'Lys-22'(PubMed:10066435). SCF(BTRC) mediates the ubiquitination of CEP68;this is required for centriole separation during mitosis(PubMed:25704143, PubMed:25503564). SCF(BTRC) mediates theubiquitination and subsequent degradation of nuclear NFE2L1 (Bysimilarity). Has an essential role in the control of the clock-dependent transcription via degradation of phosphorylated PER1 andPER2 (PubMed:15917222). May be involved in ubiquitination andsubsequent proteasomal degradation through a DBB1-CUL4 E3ubiquitin-protein ligase. Required for activation of NFKB-mediatedtranscription by IL1B, MAP3K14, MAP3K1, IKBKB and TNF. Requiredfor proteolytic processing of GLI3 (PubMed:16371461).{ECO:0000250|UniProtKB:Q3ULA2, ECO:0000269|PubMed:10066435,ECO:0000269|PubMed:10497169, ECO:0000269|PubMed:10644755,ECO:0000269|PubMed:10835356, ECO:0000269|PubMed:11238952,ECO:0000269|PubMed:11359933, ECO:0000269|PubMed:11994270,ECO:0000269|PubMed:12077367, ECO:0000269|PubMed:12791267,ECO:0000269|PubMed:12820959, ECO:0000269|PubMed:12902344,ECO:0000269|PubMed:14603323, ECO:0000269|PubMed:14681206,ECO:0000269|PubMed:14988407, ECO:0000269|PubMed:15448698,ECO:0000269|PubMed:15917222, ECO:0000269|PubMed:16371461,ECO:0000269|PubMed:25503564, ECO:0000269|PubMed:25704143,ECO:0000269|PubMed:9859996}. Auxiliary component of the splicing-dependentmultiprotein exon junction complex (EJC) deposited at splicejunction on mRNAs. The EJC is a dynamic structure consisting ofcore proteins and several peripheral nuclear and cytoplasmicassociated factors that join the complex only transiently eitherduring EJC assembly or during subsequent mRNA metabolism.Component of the ASAP complexes which bind RNA in a sequence-independent manner and are proposed to be recruited to the EJCprior to or during the splicing process and to regulate specificexcision of introns in specific transcription subsets; ACIN1confers RNA-binding to the complex. The ASAP complex can inhibitRNA processing during in vitro splicing reactions. The ASAPcomplex promotes apoptosis and is disassembled after induction ofapoptosis. Involved in the splicing modulation of BCL2L1/Bcl-X(and probably other apoptotic genes); specifically inhibitsformation of proapoptotic isoforms such as Bcl-X(S); the activityis different from the established EJC assembly and function.Induces apoptotic chromatin condensation after activation byCASP3. Regulates cyclin A1, but not cyclin A2, expression inleukemia cells. {ECO:0000269|PubMed:10490026,ECO:0000269|PubMed:12665594, ECO:0000269|PubMed:18559500,ECO:0000269|PubMed:22203037, ECO:0000269|PubMed:22388736}.

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 BTRC_ACIN1


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 BTRC_ACIN1


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 BTRC_ACIN1


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 BTRC_ACIN1


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