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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: 2638

FusionGeneSummary for ARID1B_SESTD1

check button Fusion gene summary
Fusion gene informationFusion gene name: ARID1B_SESTD1
Fusion gene ID: 2638
HgeneTgene
Gene symbol

ARID1B

SESTD1

Gene ID

57492

91404

Gene nameAT-rich interaction domain 1BSEC14 and spectrin domain containing 1
Synonyms6A3-5|BAF250B|BRIGHT|CSS1|DAN15|ELD/OSA1|MRD12|OSA2|P250RSOLO
Cytomap

6q25.3

2q31.2

Type of geneprotein-codingprotein-coding
DescriptionAT-rich interactive domain-containing protein 1BARID domain-containing protein 1BAT rich interactive domain 1B (SWI1-like)BRG1-associated factor 250bBRG1-binding protein ELD/OSA1ELD (eyelid)/OSA proteinSEC14 domain and spectrin repeat-containing protein 1SEC14 and spectrin domains 1huntingtin-interacting protein-like proteinprotein Solo
Modification date2018052920180519
UniProtAcc

Q8NFD5

Q86VW0

Ensembl transtripts involved in fusion geneENST00000350026, ENST00000346085, 
ENST00000367148, ENST00000275248, 
ENST00000478761, 
ENST00000428443, 
ENST00000486468, 
Fusion gene scores* DoF score20 X 12 X 11=26402 X 2 X 1=4
# samples 212
** MAII scorelog2(21/2640*10)=-3.65207669657969
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: ARID1B [Title/Abstract] AND SESTD1 [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

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
ChiTaRS3.1AW952707ARID1Bchr6

157107997

-SESTD1chr2

179982313

-
* 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-3CDSENST00000350026ENST00000428443ARID1Bchr6

157107997

-SESTD1chr2

179982313

-
intron-intronENST00000350026ENST00000486468ARID1Bchr6

157107997

-SESTD1chr2

179982313

-
intron-3CDSENST00000346085ENST00000428443ARID1Bchr6

157107997

-SESTD1chr2

179982313

-
intron-intronENST00000346085ENST00000486468ARID1Bchr6

157107997

-SESTD1chr2

179982313

-
intron-3CDSENST00000367148ENST00000428443ARID1Bchr6

157107997

-SESTD1chr2

179982313

-
intron-intronENST00000367148ENST00000486468ARID1Bchr6

157107997

-SESTD1chr2

179982313

-
intron-3CDSENST00000275248ENST00000428443ARID1Bchr6

157107997

-SESTD1chr2

179982313

-
intron-intronENST00000275248ENST00000486468ARID1Bchr6

157107997

-SESTD1chr2

179982313

-
intron-3CDSENST00000478761ENST00000428443ARID1Bchr6

157107997

-SESTD1chr2

179982313

-
intron-intronENST00000478761ENST00000486468ARID1Bchr6

157107997

-SESTD1chr2

179982313

-

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FusionProtFeatures for ARID1B_SESTD1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ARID1B

Q8NFD5

SESTD1

Q86VW0

Involved in transcriptional activation and repression ofselect genes by chromatin remodeling (alteration of DNA-nucleosometopology). Component of SWI/SNF chromatin remodeling complexesthat carry out key enzymatic activities, changing chromatinstructure by altering DNA-histone contacts within a nucleosome inan ATP-dependent manner. Belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and theneuron-specific chromatin remodeling complex (nBAF complex).During neural development a switch from a stem/progenitor to apostmitotic chromatin remodeling mechanism occurs as neurons exitthe cell cycle and become committed to their adult state. Thetransition from proliferating neural stem/progenitor cells topostmitotic neurons requires a switch in subunit composition ofthe npBAF and nBAF complexes. As neural progenitors exit mitosisand differentiate into neurons, npBAF complexes which containACTL6A/BAF53A and PHF10/BAF45A, are exchanged for homologousalternative ACTL6B/BAF53B and DPF1/BAF45B or DPF3/BAF45C subunitsin neuron-specific complexes (nBAF). The npBAF complex isessential for the self-renewal/proliferative capacity of themultipotent neural stem cells. The nBAF complex along with CRESTplays a role regulating the activity of genes essential fordendrite growth (By similarity). Binds DNA non-specifically(PubMed:14982958, PubMed:15170388). {ECO:0000250|UniProtKB:E9Q4N7,ECO:0000269|PubMed:14982958, ECO:0000269|PubMed:15170388,ECO:0000303|PubMed:12672490, ECO:0000303|PubMed:22952240,ECO:0000303|PubMed:26601204}. May act as the primary docking protein directingmembrane turnover and assembly of the transient receptor potentialchannels TRPC4 and TRPC5. Binds phospholipids such asphosphatidylinositol monophosphates, phosphatidylinositoldiphosphates (PIP2s) and phosphatidic acid, but not less polarlipids including phosphatidylcholine, phosphatidylserine, andphosphatidylinositol. The binding to PIP2s is calcium dependent.Might be involved in the plasma membrane localization of CTNNB1.{ECO:0000269|PubMed:20164195}.

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 ARID1B_SESTD1


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 ARID1B_SESTD1


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 ARID1B_SESTD1


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 ARID1B_SESTD1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneARID1BC0265338Coffin-Siris syndrome2CTD_human;ORPHANET
HgeneARID1BC0027819Neuroblastoma1CTD_human
HgeneARID1BC2239176Liver carcinoma1CTD_human
TgeneSESTD1C0043094Weight Gain1CTD_human