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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: 23226

FusionGeneSummary for MYPOP_RAI1

check button Fusion gene summary
Fusion gene informationFusion gene name: MYPOP_RAI1
Fusion gene ID: 23226
HgeneTgene
Gene symbol

MYPOP

RAI1

Gene ID

339344

10743

Gene nameMyb related transcription factor, partner of profilinretinoic acid induced 1
SynonymsP42popSMCR|SMS
Cytomap

19q13.32

17p11.2

Type of geneprotein-codingprotein-coding
Descriptionmyb-related transcription factor, partner of profilinmyb-related protein p42POPp42 Myb-related transcription factor, partner of profilinpartner of profilinretinoic acid-induced protein 1Smith-Magenis syndrome chromosome region
Modification date2018052320180523
UniProtAcc

Q86VE0

Q7Z5J4

Ensembl transtripts involved in fusion geneENST00000322217, ENST00000353383, 
ENST00000489697, ENST00000261641, 
Fusion gene scores* DoF score1 X 1 X 1=14 X 4 X 3=48
# samples 14
** MAII scorelog2(1/1*10)=3.32192809488736log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MYPOP [Title/Abstract] AND RAI1 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
TgeneRAI1

GO:0045893

positive regulation of transcription, DNA-templated

22578325


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
ChiTaRS3.1BG992883MYPOPchr19

46403681

-RAI1chr17

17663283

+
* 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
intron-intronENST00000322217ENST00000353383MYPOPchr19

46403681

-RAI1chr17

17663283

+
intron-intronENST00000322217ENST00000489697MYPOPchr19

46403681

-RAI1chr17

17663283

+
intron-intronENST00000322217ENST00000261641MYPOPchr19

46403681

-RAI1chr17

17663283

+

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FusionProtFeatures for MYPOP_RAI1


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

Q86VE0

RAI1

Q7Z5J4

Transcriptional repressor; DNA-binding protein thatspecifically recognizes the core sequence 5'-YAAC[GT]G-3'.Dimerization with PFN1 reduces its DNA-binding capacity (Bysimilarity). {ECO:0000250}. Transcriptional regulator of the circadian clockcomponents: CLOCK, ARNTL/BMAL1, ARNTL2/BMAL2, PER1/3, CRY1/2,NR1D1/2 and RORA/C. Positively regulates the transcriptionalactivity of CLOCK a core component of the circadian clock.Regulates transcription through chromatin remodeling byinteracting with other proteins in chromatin as well as proteinsin the basic transcriptional machinery. May be important forembryonic and postnatal development. May be involved in neuronaldifferentiation. {ECO:0000269|PubMed:22578325}.

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 MYPOP_RAI1


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 MYPOP_RAI1


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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RelatedDrugs for MYPOP_RAI1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for MYPOP_RAI1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneRAI1C0795864Smith-Magenis syndrome12CTD_human;ORPHANET
TgeneRAI1C0028754Obesity2CTD_human;HPO
TgeneRAI1C0003469Anxiety Disorders1CTD_human
TgeneRAI1C0018273Growth Disorders1CTD_human
TgeneRAI1C0025202melanoma1CTD_human
TgeneRAI1C0036341Schizophrenia1PSYGENET
TgeneRAI1C0376634Craniofacial Abnormalities1CTD_human
TgeneRAI1C0525041Neurobehavioral Manifestations1CTD_human
TgeneRAI1C0700201Dyssomnias1CTD_human
TgeneRAI1C1510586Autism Spectrum Disorders1CTD_human
TgeneRAI1C1970482Potocki-Lupski syndrome1CTD_human
TgeneRAI1C3714756Intellectual Disability1CTD_human;HPO
TgeneRAI1C3887612Psychomotor Agitation1CTD_human