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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:AMOTL1-PPIF (FusionGDB2 ID:4344)

Fusion Gene Summary for AMOTL1-PPIF

check button Fusion gene summary
Fusion gene informationFusion gene name: AMOTL1-PPIF
Fusion gene ID: 4344
HgeneTgene
Gene symbol

AMOTL1

PPIF

Gene ID

154810

10105

Gene nameangiomotin like 1peptidylprolyl isomerase F
SynonymsJEAPCYP3|CyP-M|Cyp-D|CypD
Cytomap

11q21

10q22.3

Type of geneprotein-codingprotein-coding
Descriptionangiomotin-like protein 1junction-enriched and associated proteinpeptidyl-prolyl cis-trans isomerase F, mitochondrialPPIase Fcyclophilin 3cyclophilin Dcyclophilin Fmitochondrial cyclophilinpeptidyl-prolyl cis-trans isomerase, mitochondrialrotamase F
Modification date2020031320200327
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000317829, ENST00000317837, 
ENST00000433060, ENST00000539727, 
ENST00000394579, ENST00000225174, 
ENST00000492149, 
Fusion gene scores* DoF score6 X 6 X 6=2163 X 3 X 1=9
# samples 73
** MAII scorelog2(7/216*10)=-1.6256044852185
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: AMOTL1 [Title/Abstract] AND PPIF [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointAMOTL1(94533095)-PPIF(81111311), # samples:1
Anticipated loss of major functional domain due to fusion event.AMOTL1-PPIF seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
AMOTL1-PPIF seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* 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
TgenePPIF

GO:0000413

protein peptidyl-prolyl isomerization

20676357

TgenePPIF

GO:0043066

negative regulation of apoptotic process

19228691

TgenePPIF

GO:0090201

negative regulation of release of cytochrome c from mitochondria

19228691


check buttonFusion gene breakpoints across AMOTL1 (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 PPIF (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/ABF738681AMOTL1chr11

94533095

-PPIFchr10

81111311

-


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Fusion Gene ORF analysis for AMOTL1-PPIF

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
Frame-shiftENST00000317829ENST00000394579AMOTL1chr11

94533095

-PPIFchr10

81111311

-
Frame-shiftENST00000317829ENST00000225174AMOTL1chr11

94533095

-PPIFchr10

81111311

-
5CDS-intronENST00000317829ENST00000492149AMOTL1chr11

94533095

-PPIFchr10

81111311

-
Frame-shiftENST00000317837ENST00000394579AMOTL1chr11

94533095

-PPIFchr10

81111311

-
Frame-shiftENST00000317837ENST00000225174AMOTL1chr11

94533095

-PPIFchr10

81111311

-
5CDS-intronENST00000317837ENST00000492149AMOTL1chr11

94533095

-PPIFchr10

81111311

-
Frame-shiftENST00000433060ENST00000394579AMOTL1chr11

94533095

-PPIFchr10

81111311

-
Frame-shiftENST00000433060ENST00000225174AMOTL1chr11

94533095

-PPIFchr10

81111311

-
5CDS-intronENST00000433060ENST00000492149AMOTL1chr11

94533095

-PPIFchr10

81111311

-
intron-3CDSENST00000539727ENST00000394579AMOTL1chr11

94533095

-PPIFchr10

81111311

-
intron-3CDSENST00000539727ENST00000225174AMOTL1chr11

94533095

-PPIFchr10

81111311

-
intron-intronENST00000539727ENST00000492149AMOTL1chr11

94533095

-PPIFchr10

81111311

-

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 AMOTL1-PPIF


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 AMOTL1-PPIF


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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 AMOTL1-PPIF


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 AMOTL1-PPIF


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 AMOTL1-PPIF


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 AMOTL1-PPIF


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneAMOTL1C3495676Anorectal Malformations1GENOMICS_ENGLAND
TgenePPIFC0021831Intestinal Diseases1CTD_human
TgenePPIFC0041582Ulcer1CTD_human