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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:RAP1A-MAML1 (FusionGDB2 ID:71683)

Fusion Gene Summary for RAP1A-MAML1

check button Fusion gene summary
Fusion gene informationFusion gene name: RAP1A-MAML1
Fusion gene ID: 71683
HgeneTgene
Gene symbol

RAP1A

MAML1

Gene ID

5906

9794

Gene nameRAP1A, member of RAS oncogene familymastermind like transcriptional coactivator 1
SynonymsC21KG|G-22K|KREV-1|KREV1|RAP1|SMGP21Mam-1|Mam1
Cytomap

1p13.2

5q35.3

Type of geneprotein-codingprotein-coding
Descriptionras-related protein Rap-1AGTP-binding protein smg p21ARas-related protein Krev-1mastermind-like protein 1mastermind homologmastermind-like 1
Modification date2020032920200322
UniProtAcc.

Q92585

Ensembl transtripts involved in fusion geneENST00000356415, ENST00000436150, 
ENST00000369709, ENST00000545460, 
ENST00000494982, 
ENST00000292599, 
ENST00000503050, 
Fusion gene scores* DoF score13 X 11 X 5=7155 X 5 X 4=100
# samples 136
** MAII scorelog2(13/715*10)=-2.4594316186373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/100*10)=-0.736965594166206
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RAP1A [Title/Abstract] AND MAML1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointRAP1A(112170185)-MAML1(179198148), # 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
HgeneRAP1A

GO:0071320

cellular response to cAMP

21840392

HgeneRAP1A

GO:0072659

protein localization to plasma membrane

17916086

HgeneRAP1A

GO:0098696

regulation of neurotransmitter receptor localization to postsynaptic specialization membrane

12202034

TgeneMAML1

GO:0006468

protein phosphorylation

16510869

TgeneMAML1

GO:0007219

Notch signaling pathway

11101851

TgeneMAML1

GO:0045944

positive regulation of transcription by RNA polymerase II

11101851|16510869


check buttonFusion gene breakpoints across RAP1A (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 MAML1 (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
ChimerDB4SARCTCGA-FX-A2QS-01ARAP1Achr1

112170185

+MAML1chr5

179198148

+


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Fusion Gene ORF analysis for RAP1A-MAML1

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-3CDSENST00000356415ENST00000292599RAP1Achr1

112170185

+MAML1chr5

179198148

+
intron-3UTRENST00000356415ENST00000503050RAP1Achr1

112170185

+MAML1chr5

179198148

+
5UTR-3CDSENST00000436150ENST00000292599RAP1Achr1

112170185

+MAML1chr5

179198148

+
5UTR-3UTRENST00000436150ENST00000503050RAP1Achr1

112170185

+MAML1chr5

179198148

+
intron-3CDSENST00000369709ENST00000292599RAP1Achr1

112170185

+MAML1chr5

179198148

+
intron-3UTRENST00000369709ENST00000503050RAP1Achr1

112170185

+MAML1chr5

179198148

+
intron-3CDSENST00000545460ENST00000292599RAP1Achr1

112170185

+MAML1chr5

179198148

+
intron-3UTRENST00000545460ENST00000503050RAP1Achr1

112170185

+MAML1chr5

179198148

+
3UTR-3CDSENST00000494982ENST00000292599RAP1Achr1

112170185

+MAML1chr5

179198148

+
3UTR-3UTRENST00000494982ENST00000503050RAP1Achr1

112170185

+MAML1chr5

179198148

+

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 RAP1A-MAML1


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)
RAP1Achr1112170181+MAML1chr5179198147+3.97E-070.99999964
RAP1Achr1112170181+MAML1chr5179198147+3.97E-070.99999964

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 RAP1A-MAML1


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
.MAML1

Q92585

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: Acts as a transcriptional coactivator for NOTCH proteins. Has been shown to amplify NOTCH-induced transcription of HES1. Enhances phosphorylation and proteolytic turnover of the NOTCH intracellular domain in the nucleus through interaction with CDK8. Binds to CREBBP/CBP which promotes nucleosome acetylation at NOTCH enhancers and activates transcription. Induces phosphorylation and localization of CREBBP to nuclear foci. Plays a role in hematopoietic development by regulating NOTCH-mediated lymphoid cell fate decisions. {ECO:0000269|PubMed:11101851, ECO:0000269|PubMed:11390662, ECO:0000269|PubMed:12050117, ECO:0000269|PubMed:15546612, ECO:0000269|PubMed:17317671}.

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 RAP1A-MAML1


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 RAP1A-MAML1


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 RAP1A-MAML1


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 RAP1A-MAML1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRAP1AC0796004Kabuki make-up syndrome1ORPHANET