FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:IFNAR1-RPS27A (FusionGDB2 ID:38218)

Fusion Gene Summary for IFNAR1-RPS27A

check button Fusion gene summary
Fusion gene informationFusion gene name: IFNAR1-RPS27A
Fusion gene ID: 38218
HgeneTgene
Gene symbol

IFNAR1

RPS27A

Gene ID

3454

6233

Gene nameinterferon alpha and beta receptor subunit 1ribosomal protein S27a
SynonymsAVP|IFN-alpha-REC|IFNAR|IFNBR|IFRCCEP80|HEL112|S27A|UBA80|UBC|UBCEP1|UBCEP80
Cytomap

21q22.11

2p16.1

Type of geneprotein-codingprotein-coding
Descriptioninterferon alpha/beta receptor 1CRF2-1IFN-R-1IFN-alpha/beta receptor 1alpha-type antiviral proteinbeta-type antiviral proteincytokine receptor class-II member 1cytokine receptor family 2 member 1interferon (alpha, beta and omega) receptor 1interfubiquitin-40S ribosomal protein S27a40S ribosomal protein S27aepididymis luminal protein 112ubiquitin Cubiquitin and ribosomal protein S27aubiquitin carboxyl extension protein 80ubiquitin-CEP80
Modification date2020031320200313
UniProtAcc

P17181

.
Ensembl transtripts involved in fusion geneENST00000416947, ENST00000493503, 
ENST00000270139, ENST00000442357, 
ENST00000402285, ENST00000272317, 
ENST00000404735, 
Fusion gene scores* DoF score7 X 8 X 4=22412 X 13 X 6=936
# samples 717
** MAII scorelog2(7/224*10)=-1.67807190511264
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(17/936*10)=-2.4609737834457
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: IFNAR1 [Title/Abstract] AND RPS27A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointIFNAR1(34727789)-RPS27A(55460532), # samples:1
Anticipated loss of major functional domain due to fusion event.IFNAR1-RPS27A seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
IFNAR1-RPS27A seems lost the major protein functional domain in Tgene partner, which is a cell metabolism 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
HgeneIFNAR1

GO:0060337

type I interferon signaling pathway

7665574


check buttonFusion gene breakpoints across IFNAR1 (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 RPS27A (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/ABQ946630IFNAR1chr21

34727789

+RPS27Achr2

55460532

+


Top

Fusion Gene ORF analysis for IFNAR1-RPS27A

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-shiftENST00000416947ENST00000402285IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
Frame-shiftENST00000416947ENST00000272317IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
Frame-shiftENST00000416947ENST00000404735IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
intron-3CDSENST00000493503ENST00000402285IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
intron-3CDSENST00000493503ENST00000272317IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
intron-3CDSENST00000493503ENST00000404735IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
Frame-shiftENST00000270139ENST00000402285IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
Frame-shiftENST00000270139ENST00000272317IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
Frame-shiftENST00000270139ENST00000404735IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
Frame-shiftENST00000442357ENST00000402285IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
Frame-shiftENST00000442357ENST00000272317IFNAR1chr21

34727789

+RPS27Achr2

55460532

+
Frame-shiftENST00000442357ENST00000404735IFNAR1chr21

34727789

+RPS27Achr2

55460532

+

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

Top

Fusion Genomic Features for IFNAR1-RPS27A


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.

Top

Fusion Protein Features for IFNAR1-RPS27A


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
IFNAR1

P17181

.
FUNCTION: Component of the receptor for type I interferons, including interferons alpha, IFNB1 and IFNW1 (PubMed:2153461, PubMed:7665574, PubMed:10049744, PubMed:14532120, PubMed:15337770, PubMed:21854986). Functions in general as heterodimer with IFNAR2 (PubMed:7665574, PubMed:10049744, PubMed:21854986). Type I interferon binding activates the JAK-STAT signaling cascade, and triggers tyrosine phosphorylation of a number of proteins including JAKs, TYK2, STAT proteins and the IFNR alpha- and beta-subunits themselves (PubMed:7665574, PubMed:21854986, PubMed:32972995). Can form an active IFNB1 receptor by itself and activate a signaling cascade that does not involve activation of the JAK-STAT pathway (By similarity). {ECO:0000250|UniProtKB:P33896, ECO:0000269|PubMed:10049744, ECO:0000269|PubMed:14532120, ECO:0000269|PubMed:15337770, ECO:0000269|PubMed:19561067, ECO:0000269|PubMed:2153461, ECO:0000269|PubMed:32972995, ECO:0000269|PubMed:7665574, ECO:0000305|PubMed:21854986}.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


Top

Fusion Gene Sequence for IFNAR1-RPS27A


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.

Top

Fusion Gene PPI Analysis for IFNAR1-RPS27A


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


Top

Related Drugs for IFNAR1-RPS27A


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneIFNAR1P17181DB00022Peginterferon alfa-2bAgonistBiotechApproved
HgeneIFNAR1P17181DB00022Peginterferon alfa-2bAgonistBiotechApproved
HgeneIFNAR1P17181DB00068Interferon beta-1bAgonistBiotechApproved
HgeneIFNAR1P17181DB00068Interferon beta-1bAgonistBiotechApproved
HgeneIFNAR1P17181DB00105Interferon alfa-2bBinderBiotechApproved
HgeneIFNAR1P17181DB00105Interferon alfa-2bBinderBiotechApproved
HgeneIFNAR1P17181DB00008Peginterferon alfa-2aAgonistBiotechApproved|Investigational
HgeneIFNAR1P17181DB00008Peginterferon alfa-2aAgonistBiotechApproved|Investigational
HgeneIFNAR1P17181DB00011Interferon alfa-n1AgonistBiotechApproved|Investigational
HgeneIFNAR1P17181DB00011Interferon alfa-n1AgonistBiotechApproved|Investigational
HgeneIFNAR1P17181DB00018Interferon alfa-n3AgonistBiotechApproved|Investigational
HgeneIFNAR1P17181DB00018Interferon alfa-n3AgonistBiotechApproved|Investigational
HgeneIFNAR1P17181DB00034Interferon alfa-2a, RecombinantBiotechApproved|Investigational
HgeneIFNAR1P17181DB00034Interferon alfa-2a, RecombinantBiotechApproved|Investigational
HgeneIFNAR1P17181DB00060Interferon beta-1aAgonistBiotechApproved|Investigational
HgeneIFNAR1P17181DB00060Interferon beta-1aAgonistBiotechApproved|Investigational
HgeneIFNAR1P17181DB00069Interferon alfacon-1BinderBiotechApproved|Investigational
HgeneIFNAR1P17181DB00069Interferon alfacon-1BinderBiotechApproved|Investigational
HgeneIFNAR1P17181DB14999Human interferon betaBinderBiotechApproved|Investigational
HgeneIFNAR1P17181DB14999Human interferon betaBinderBiotechApproved|Investigational

Top

Related Diseases for IFNAR1-RPS27A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneIFNAR1C0042769Virus Diseases1CTD_human
HgeneIFNAR1C0086132Depressive Symptoms1PSYGENET
HgeneIFNAR1C0338715Drug-induced depressive state1PSYGENET
TgeneRPS27AC1260899Anemia, Diamond-Blackfan1GENOMICS_ENGLAND