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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: 32400

FusionGeneSummary for RUNX1_IFNAR1

check button Fusion gene summary
Fusion gene informationFusion gene name: RUNX1_IFNAR1
Fusion gene ID: 32400
HgeneTgene
Gene symbol

RUNX1

IFNAR1

Gene ID

861

3454

Gene namerunt related transcription factor 1interferon alpha and beta receptor subunit 1
SynonymsAML1|AML1-EVI-1|AMLCR1|CBF2alpha|CBFA2|EVI-1|PEBP2aB|PEBP2alphaAVP|IFN-alpha-REC|IFNAR|IFNBR|IFRC
Cytomap

21q22.12

21q22.11

Type of geneprotein-codingprotein-coding
Descriptionrunt-related transcription factor 1AML1-EVI-1 fusion proteinPEA2-alpha BPEBP2-alpha BSL3-3 enhancer factor 1 alpha B subunitSL3/AKV core-binding factor alpha B subunitacute myeloid leukemia 1 proteincore-binding factor, runt domain, alpha subunit 2interferon 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 1interf
Modification date2018052720180523
UniProtAcc

Q01196

P17181

Ensembl transtripts involved in fusion geneENST00000344691, ENST00000325074, 
ENST00000437180, ENST00000300305, 
ENST00000399240, ENST00000486278, 
ENST00000494829, ENST00000358356, 
ENST00000416947, ENST00000493503, 
ENST00000270139, ENST00000442357, 
Fusion gene scores* DoF score23 X 25 X 7=40255 X 5 X 2=50
# samples 535
** MAII scorelog2(53/4025*10)=-2.92492451843878
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(5/50*10)=0
Context

PubMed: RUNX1 [Title/Abstract] AND IFNAR1 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotationTumor suppressor gene involved fusion gene, retained protein feature but frameshift.
DDR (DNA damage repair) gene involved fusion gene, in-frame but not retained their domain.
* 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
HgeneRUNX1

GO:0030097

hemopoiesis

21873977

HgeneRUNX1

GO:0045893

positive regulation of transcription, DNA-templated

10207087|14970218

HgeneRUNX1

GO:0045944

positive regulation of transcription by RNA polymerase II

9199349|10207087|14970218|21873977

TgeneIFNAR1

GO:0060337

type I interferon signaling pathway

7665574


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
TCGARVSKCMTCGA-DA-A3F5-06ARUNX1chr21

36206707

-IFNAR1chr21

34725064

+
* 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
Frame-shiftENST00000344691ENST00000416947RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000344691ENST00000493503RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000344691ENST00000270139RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000344691ENST00000442357RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
Frame-shiftENST00000325074ENST00000416947RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000325074ENST00000493503RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000325074ENST00000270139RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000325074ENST00000442357RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
Frame-shiftENST00000437180ENST00000416947RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000437180ENST00000493503RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000437180ENST00000270139RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000437180ENST00000442357RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
Frame-shiftENST00000300305ENST00000416947RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000300305ENST00000493503RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000300305ENST00000270139RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000300305ENST00000442357RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-3CDSENST00000399240ENST00000416947RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-intronENST00000399240ENST00000493503RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-intronENST00000399240ENST00000270139RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-intronENST00000399240ENST00000442357RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-3CDSENST00000486278ENST00000416947RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-intronENST00000486278ENST00000493503RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-intronENST00000486278ENST00000270139RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-intronENST00000486278ENST00000442357RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-3CDSENST00000494829ENST00000416947RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-intronENST00000494829ENST00000493503RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-intronENST00000494829ENST00000270139RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
intron-intronENST00000494829ENST00000442357RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
Frame-shiftENST00000358356ENST00000416947RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000358356ENST00000493503RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000358356ENST00000270139RUNX1chr21

36206707

-IFNAR1chr21

34725064

+
5CDS-intronENST00000358356ENST00000442357RUNX1chr21

36206707

-IFNAR1chr21

34725064

+

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FusionProtFeatures for RUNX1_IFNAR1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RUNX1

Q01196

IFNAR1

P17181


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 RUNX1_IFNAR1


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 RUNX1_IFNAR1


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
RUNX1SUV39H1, KAT6B, CBFB, AES, PAX5, YAP1, JUN, FOS, SMAD3, SMAD1, SMAD2, SMAD5, VDR, ELF4, ELF2, CEBPB, TLE1, CBFA2T2, TRAF6, FHL2, MYOD1, HIPK2, EP300, HDAC1, HDAC3, KAT6A, TCF12, TCF3, RUNX1T1, NCOR1, SIAH1, UBE2L6, RUNX1, PML, RARA, HDAC2, SIN3A, NR4A2, TRIM33, STUB1, SMARCA4, SMARCB1, SMARCC1, CDK1, TAL1, COPRS, KMT2A, RBM14, SPEN, DNMT1, ELAVL1, CBFA2T3, PRMT1, HLA-DMA, CREBBP, UXT, CTBP2, NOTCH1, MYC, NCOR2, FOXP3, SOX2, CTBP1, HDAC11, RAG1, SPI1, ELF1, CDK6, KLF6, NFATC1, NFATC2, ZNF131, BRCA1, CDK9, FANCD2IFNAR1PRMT1, TYK2, STAT2, PIK3R1, STAT3, AP2M1, FBXW11, BTRC, PRKD2, SOCS1, STAT6, GNB2L1, IFNAR2, IFNB1, TNFRSF10A, TRIM25, USP7


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 RUNX1_IFNAR1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneIFNAR1P17181DB00022Peginterferon alfa-2bInterferon alpha/beta receptor 1biotechapproved
TgeneIFNAR1P17181DB00068Interferon beta-1bInterferon alpha/beta receptor 1biotechapproved
TgeneIFNAR1P17181DB00105Interferon Alfa-2b, RecombinantInterferon alpha/beta receptor 1biotechapproved
TgeneIFNAR1P17181DB00008Peginterferon alfa-2aInterferon alpha/beta receptor 1biotechapproved|investigational
TgeneIFNAR1P17181DB00011Interferon alfa-n1Interferon alpha/beta receptor 1biotechapproved|investigational
TgeneIFNAR1P17181DB00034Interferon Alfa-2a, RecombinantInterferon alpha/beta receptor 1biotechapproved|investigational
TgeneIFNAR1P17181DB00060Interferon beta-1aInterferon alpha/beta receptor 1biotechapproved|investigational
TgeneIFNAR1P17181DB00069Interferon alfacon-1Interferon alpha/beta receptor 1biotechapproved|investigational

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RelatedDiseases for RUNX1_IFNAR1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRUNX1C0023467Leukemia, Myelocytic, Acute2CTD_human;HPO
HgeneRUNX1C0023485Precursor B-Cell Lymphoblastic Leukemia-Lymphoma2CTD_human
HgeneRUNX1C0003873Rheumatoid Arthritis1CTD_human
HgeneRUNX1C0017636Glioblastoma1CTD_human
HgeneRUNX1C0033578Prostatic Neoplasms1CTD_human
HgeneRUNX1C0349639Juvenile Myelomonocytic Leukemia1CTD_human
HgeneRUNX1C1832388Platelet Disorder, Familial, with Associated Myeloid Malignancy1CTD_human;ORPHANET;UNIPROT
HgeneRUNX1C1961102Precursor Cell Lymphoblastic Leukemia Lymphoma1CTD_human
TgeneIFNAR1C0042769Virus Diseases1CTD_human
TgeneIFNAR1C0086132Depressive Symptoms1PSYGENET
TgeneIFNAR1C0338715Drug-induced depressive state1PSYGENET