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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:CPT1A-FGG (FusionGDB2 ID:19215)

Fusion Gene Summary for CPT1A-FGG

check button Fusion gene summary
Fusion gene informationFusion gene name: CPT1A-FGG
Fusion gene ID: 19215
HgeneTgene
Gene symbol

CPT1A

FGG

Gene ID

1374

2266

Gene namecarnitine palmitoyltransferase 1Afibrinogen gamma chain
SynonymsCPT1|CPT1-L|L-CPT1-
Cytomap

11q13.3

4q32.1

Type of geneprotein-codingprotein-coding
Descriptioncarnitine O-palmitoyltransferase 1, liver isoformCPT ICPTI-Lcarnitine O-palmitoyltransferase I, liver isoformcarnitine palmitoyltransferase 1A (liver)carnitine palmitoyltransferase I, liverfibrinogen gamma chainfibrinogen, gamma polypeptidetesticular tissue protein Li 70
Modification date2020031520200329
UniProtAcc

P50416

Q96C11

Ensembl transtripts involved in fusion geneENST00000265641, ENST00000376618, 
ENST00000537756, ENST00000538994, 
ENST00000539743, ENST00000540367, 
ENST00000336098, ENST00000404648, 
ENST00000405164, ENST00000407946, 
Fusion gene scores* DoF score25 X 23 X 12=69009 X 11 X 4=396
# samples 3211
** MAII scorelog2(32/6900*10)=-4.43045255166553
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/396*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CPT1A [Title/Abstract] AND FGG [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCPT1A(68523409)-FGG(155526135), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneCPT1A

GO:0001676

long-chain fatty acid metabolic process

11350182

HgeneCPT1A

GO:0009437

carnitine metabolic process

11350182

TgeneFGG

GO:0007160

cell-matrix adhesion

10903502

TgeneFGG

GO:0031639

plasminogen activation

16846481

TgeneFGG

GO:0034116

positive regulation of heterotypic cell-cell adhesion

8100742

TgeneFGG

GO:0034622

cellular protein-containing complex assembly

8910396

TgeneFGG

GO:0042730

fibrinolysis

16846481

TgeneFGG

GO:0045907

positive regulation of vasoconstriction

15739255

TgeneFGG

GO:0045921

positive regulation of exocytosis

19193866

TgeneFGG

GO:0050714

positive regulation of protein secretion

19193866

TgeneFGG

GO:0051592

response to calcium ion

6777381

TgeneFGG

GO:0070374

positive regulation of ERK1 and ERK2 cascade

10903502|19193866

TgeneFGG

GO:0070527

platelet aggregation

6281794

TgeneFGG

GO:0072378

blood coagulation, fibrin clot formation

16846481

TgeneFGG

GO:0090277

positive regulation of peptide hormone secretion

19193866

TgeneFGG

GO:1902042

negative regulation of extrinsic apoptotic signaling pathway via death domain receptors

10903502

TgeneFGG

GO:2000352

negative regulation of endothelial cell apoptotic process

10903502


check buttonFusion gene breakpoints across CPT1A (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across FGG (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ACB154699CPT1Achr11

68523409

+FGGchr4

155526135

-


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Fusion Gene ORF analysis for CPT1A-FGG

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-3CDSENST00000265641ENST00000336098CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000265641ENST00000404648CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000265641ENST00000405164CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000265641ENST00000407946CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000376618ENST00000336098CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000376618ENST00000404648CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000376618ENST00000405164CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000376618ENST00000407946CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000537756ENST00000336098CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000537756ENST00000404648CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000537756ENST00000405164CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000537756ENST00000407946CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000538994ENST00000336098CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000538994ENST00000404648CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000538994ENST00000405164CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000538994ENST00000407946CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000539743ENST00000336098CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000539743ENST00000404648CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000539743ENST00000405164CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000539743ENST00000407946CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000540367ENST00000336098CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000540367ENST00000404648CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000540367ENST00000405164CPT1Achr11

68523409

+FGGchr4

155526135

-
intron-3CDSENST00000540367ENST00000407946CPT1Achr11

68523409

+FGGchr4

155526135

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for CPT1A-FGG


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for CPT1A-FGG


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:68523409/:155526135)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CPT1A

P50416

FGG

Q96C11

FUNCTION: Catalyzes the transfer of the acyl group of long-chain fatty acid-CoA conjugates onto carnitine, an essential step for the mitochondrial uptake of long-chain fatty acids and their subsequent beta-oxidation in the mitochondrion (PubMed:9691089, PubMed:11350182, PubMed:14517221). Plays an important role in hepatic triglyceride metabolism (By similarity). {ECO:0000250|UniProtKB:P32198, ECO:0000269|PubMed:11350182, ECO:0000269|PubMed:14517221, ECO:0000269|PubMed:9691089}.

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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Fusion Gene Sequence for CPT1A-FGG


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for CPT1A-FGG


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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Related Drugs for CPT1A-FGG


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for CPT1A-FGG


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