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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: 4371

FusionGeneSummary for BRAP_CPT1B

check button Fusion gene summary
Fusion gene informationFusion gene name: BRAP_CPT1B
Fusion gene ID: 4371
HgeneTgene
Gene symbol

BRAP

CPT1B

Gene ID

221477

1375

Gene namechromosome 6 open reading frame 89carnitine palmitoyltransferase 1B
SynonymsBRAP|PS1TP5TP1CPT1-M|CPT1M|CPTI|CPTI-M|M-CPT1|MCCPT1|MCPT1
Cytomap

6p21.2

22q13.33

Type of geneprotein-codingprotein-coding
Descriptionbombesin receptor-activated protein C6orf89amfioncarnitine O-palmitoyltransferase 1, muscle isoformcarnitine O-palmitoyltransferase 1Bcarnitine O-palmitoyltransferase I, mitochondrial muscle isoformcarnitine palmitoyltransferase 1B (muscle)carnitine palmitoyltransferase I-like protein
Modification date2018051920180523
UniProtAcc

Q7Z569

Q92523

Ensembl transtripts involved in fusion geneENST00000419234, ENST00000539060, 
ENST00000327551, 
ENST00000405237, 
ENST00000312108, ENST00000440709, 
ENST00000360719, ENST00000457250, 
ENST00000434492, ENST00000395650, 
Fusion gene scores* DoF score4 X 4 X 4=642 X 2 X 2=8
# samples 42
** MAII scorelog2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: BRAP [Title/Abstract] AND CPT1B [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
HgeneBRAP

GO:0042060

wound healing

21857995

HgeneBRAP

GO:0045787

positive regulation of cell cycle

21857995

HgeneBRAP

GO:0050673

epithelial cell proliferation

21857995

HgeneBRAP

GO:1901727

positive regulation of histone deacetylase activity

23460338


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
ChiTaRS3.1DB055888BRAPchr12

112123685

-CPT1Bchr22

51016368

-
* 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-5UTRENST00000419234ENST00000405237BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000419234ENST00000312108BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000419234ENST00000440709BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000419234ENST00000360719BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000419234ENST00000457250BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000419234ENST00000434492BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000419234ENST00000395650BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000539060ENST00000405237BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000539060ENST00000312108BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000539060ENST00000440709BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000539060ENST00000360719BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000539060ENST00000457250BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000539060ENST00000434492BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000539060ENST00000395650BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000327551ENST00000405237BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000327551ENST00000312108BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000327551ENST00000440709BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000327551ENST00000360719BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000327551ENST00000457250BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000327551ENST00000434492BRAPchr12

112123685

-CPT1Bchr22

51016368

-
intron-5UTRENST00000327551ENST00000395650BRAPchr12

112123685

-CPT1Bchr22

51016368

-

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FusionProtFeatures for BRAP_CPT1B


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

Q7Z569

CPT1B

Q92523

Negatively regulates MAP kinase activation by limitingthe formation of Raf/MEK complexes probably by inactivation of theKSR1 scaffold protein. Also acts as a Ras responsive E3 ubiquitinligase that, on activation of Ras, is modified by auto-polyubiquitination resulting in the release of inhibition ofRaf/MEK complex formation. May also act as a cytoplasmic retentionprotein with a role in regulating nuclear transport.{ECO:0000269|PubMed:14724641, ECO:0000303|PubMed:10777491}.

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 BRAP_CPT1B


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 BRAP_CPT1B


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 BRAP_CPT1B


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 BRAP_CPT1B


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneBRAPC0027051Myocardial Infarction1CTD_human
HgeneBRAPC0036341Schizophrenia1PSYGENET
TgeneCPT1BC0011853Diabetes Mellitus, Experimental1CTD_human
TgeneCPT1BC0018800Cardiomegaly1CTD_human
TgeneCPT1BC0023903Liver neoplasms1CTD_human
TgeneCPT1BC0027404Narcolepsy1CTD_human
TgeneCPT1BC0151744Myocardial Ischemia1CTD_human