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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: 30986

FusionGeneSummary for REST_CNOT1

check button Fusion gene summary
Fusion gene informationFusion gene name: REST_CNOT1
Fusion gene ID: 30986
HgeneTgene
Gene symbol

REST

CNOT1

Gene ID

5978

23019

Gene nameRE1 silencing transcription factorCCR4-NOT transcription complex subunit 1
SynonymsGINGF5|HGF5|NRSF|WT6|XBRAD-005|CDC39|NOT1|NOT1H
Cytomap

4q12

16q21

Type of geneprotein-codingprotein-coding
DescriptionRE1-silencing transcription factorneural-restrictive silencer factorneuron restrictive silencer factorrepressor binding to the X2 boxCCR4-NOT transcription complex subunit 1CCR4-associated factor 1NOT1 (negative regulator of transcription 1, yeast) homologadrenal gland protein AD-005negative regulator of transcription subunit 1 homolog
Modification date2018052320180523
UniProtAcc

Q13127

A5YKK6

Ensembl transtripts involved in fusion geneENST00000309042, ENST00000514063, 
ENST00000317147, ENST00000569240, 
ENST00000441024, ENST00000569732, 
ENST00000245138, 
Fusion gene scores* DoF score4 X 4 X 1=164 X 5 X 3=60
# samples 45
** MAII scorelog2(4/16*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: REST [Title/Abstract] AND CNOT1 [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
HgeneREST

GO:0000122

negative regulation of transcription by RNA polymerase II

8568247|21284946

HgeneREST

GO:0043922

negative regulation by host of viral transcription

17555596

HgeneREST

GO:0045892

negative regulation of transcription, DNA-templated

7697725|10449787|10734093|17984088|19342457

HgeneREST

GO:0045893

positive regulation of transcription, DNA-templated

17984088

HgeneREST

GO:0070933

histone H4 deacetylation

17555596

HgeneREST

GO:0071385

cellular response to glucocorticoid stimulus

17984088

TgeneCNOT1

GO:0000122

negative regulation of transcription by RNA polymerase II

16778766

TgeneCNOT1

GO:0010606

positive regulation of cytoplasmic mRNA processing body assembly

21976065

TgeneCNOT1

GO:0017148

negative regulation of translation

24736845

TgeneCNOT1

GO:0033147

negative regulation of intracellular estrogen receptor signaling pathway

16778766

TgeneCNOT1

GO:0035195

gene silencing by miRNA

23172285|24768540

TgeneCNOT1

GO:0048387

negative regulation of retinoic acid receptor signaling pathway

16778766

TgeneCNOT1

GO:0060213

positive regulation of nuclear-transcribed mRNA poly(A) tail shortening

23644599


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
ChiTaRS3.1U22680RESTchr4

57800857

+CNOT1chr16

58559926

+
* 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
3UTR-3CDSENST00000309042ENST00000317147RESTchr4

57800857

+CNOT1chr16

58559926

+
3UTR-3CDSENST00000309042ENST00000569240RESTchr4

57800857

+CNOT1chr16

58559926

+
3UTR-intronENST00000309042ENST00000441024RESTchr4

57800857

+CNOT1chr16

58559926

+
3UTR-intronENST00000309042ENST00000569732RESTchr4

57800857

+CNOT1chr16

58559926

+
3UTR-intronENST00000309042ENST00000245138RESTchr4

57800857

+CNOT1chr16

58559926

+
intron-3CDSENST00000514063ENST00000317147RESTchr4

57800857

+CNOT1chr16

58559926

+
intron-3CDSENST00000514063ENST00000569240RESTchr4

57800857

+CNOT1chr16

58559926

+
intron-intronENST00000514063ENST00000441024RESTchr4

57800857

+CNOT1chr16

58559926

+
intron-intronENST00000514063ENST00000569732RESTchr4

57800857

+CNOT1chr16

58559926

+
intron-intronENST00000514063ENST00000245138RESTchr4

57800857

+CNOT1chr16

58559926

+

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FusionProtFeatures for REST_CNOT1


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

Q13127

CNOT1

A5YKK6

Transcriptional repressor which binds neuron-restrictivesilencer element (NRSE) and represses neuronal gene transcriptionin non-neuronal cells. Restricts the expression of neuronal genesby associating with two distinct corepressors, mSin3 and CoREST,which in turn recruit histone deacetylase to the promoters ofREST-regulated genes. Mediates repression by recruiting the BHCcomplex at RE1/NRSE sites which acts by deacetylating anddemethylating specific sites on histones, thereby acting as achromatin modifier. Transcriptional repression by REST-CDYL viathe recruitment of histone methyltransferase EHMT2 may beimportant in transformation suppression.{ECO:0000269|PubMed:12399542, ECO:0000269|PubMed:19061646,ECO:0000269|PubMed:26551668, ECO:0000269|PubMed:7697725,ECO:0000269|PubMed:7871435, ECO:0000269|PubMed:8568247}.

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 REST_CNOT1


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 REST_CNOT1


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 REST_CNOT1


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 REST_CNOT1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRESTC0015923Fetal Alcohol Syndrome1PSYGENET
HgeneRESTC0027708Nephroblastoma1CTD_human;HPO;ORPHANET
HgeneRESTC0036341Schizophrenia1PSYGENET
HgeneRESTC0036572Seizures1CTD_human
HgeneRESTC1269683Major Depressive Disorder1PSYGENET
HgeneRESTC3891301WILMS TUMOR, SUSCEPTIBILITY TO1UNIPROT