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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: 34835

FusionGeneSummary for SMARCC2_SELENBP1

check button Fusion gene summary
Fusion gene informationFusion gene name: SMARCC2_SELENBP1
Fusion gene ID: 34835
HgeneTgene
Gene symbol

SMARCC2

SELENBP1

Gene ID

6601

8991

Gene nameSWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2selenium binding protein 1
SynonymsBAF170|CRACC2|Rsc8HEL-S-134P|LPSB|MTO|SBP56|SP56|hSBP
Cytomap

12q13.2

1q21.3

Type of geneprotein-codingprotein-coding
DescriptionSWI/SNF complex subunit SMARCC2SWI/SNF complex 170 kDa subunitSWI3-like proteinchromatin remodeling complex BAF170 subunitmammalian chromatin remodeling complex BRG1-associated factor 170methanethiol oxidaseselenium-binding protein 156 kDa selenium-binding proteinepididymis secretory sperm binding protein Li 134P
Modification date2018051920180519
UniProtAcc

Q8TAQ2

Q13228

Ensembl transtripts involved in fusion geneENST00000394023, ENST00000550164, 
ENST00000347471, ENST00000267064, 
ENST00000550859, 
ENST00000368868, 
ENST00000447402, ENST00000426705, 
ENST00000435071, ENST00000473693, 
Fusion gene scores* DoF score7 X 7 X 3=1474 X 6 X 4=96
# samples 77
** MAII scorelog2(7/147*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/96*10)=-0.45567948377619
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SMARCC2 [Title/Abstract] AND SELENBP1 [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
HgeneSMARCC2

GO:0006337

nucleosome disassembly

8895581

HgeneSMARCC2

GO:0006338

chromatin remodeling

10078207|11018012|11726552

HgeneSMARCC2

GO:0045892

negative regulation of transcription, DNA-templated

12192000

HgeneSMARCC2

GO:0045893

positive regulation of transcription, DNA-templated

11018012


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
ChiTaRS3.1AW603757SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
* 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-3UTRENST00000394023ENST00000368868SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000394023ENST00000447402SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000394023ENST00000426705SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000394023ENST00000435071SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-intronENST00000394023ENST00000473693SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000550164ENST00000368868SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000550164ENST00000447402SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000550164ENST00000426705SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000550164ENST00000435071SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-intronENST00000550164ENST00000473693SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000347471ENST00000368868SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000347471ENST00000447402SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000347471ENST00000426705SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000347471ENST00000435071SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-intronENST00000347471ENST00000473693SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000267064ENST00000368868SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000267064ENST00000447402SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000267064ENST00000426705SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000267064ENST00000435071SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-intronENST00000267064ENST00000473693SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000550859ENST00000368868SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000550859ENST00000447402SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000550859ENST00000426705SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-3UTRENST00000550859ENST00000435071SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+
intron-intronENST00000550859ENST00000473693SMARCC2chr12

56563975

-SELENBP1chr1

151336946

+

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FusionProtFeatures for SMARCC2_SELENBP1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SMARCC2

Q8TAQ2

SELENBP1

Q13228

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 (PubMed:11018012). Can stimulate theATPase activity of the catalytic subunit of these complexes(PubMed:10078207). May be required for CoREST dependent repressionof neuronal specific gene promoters in non-neuronal cells(PubMed:12192000). Belongs to the neural progenitors-specificchromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). Duringneural 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). Critical regulator of myeloiddifferentiation, controlling granulocytopoiesis and the expressionof genes involved in neutrophil granule formation (By similarity).{ECO:0000250|UniProtKB:Q6PDG5, ECO:0000269|PubMed:10078207,ECO:0000269|PubMed:11018012, ECO:0000269|PubMed:12192000,ECO:0000303|PubMed:22952240, ECO:0000303|PubMed:26601204}. Catalyzes the oxidation of methanethiol, an organosulfurcompound known to be produced in substantial amounts by gutbacteria (PubMed:29255262). Selenium-binding protein which may beinvolved in the sensing of reactive xenobiotics in the cytoplasm.May be involved in intra-Golgi protein transport (By similarity).{ECO:0000250|UniProtKB:Q8VIF7, ECO:0000269|PubMed:29255262}.

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 SMARCC2_SELENBP1


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 SMARCC2_SELENBP1


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 SMARCC2_SELENBP1


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 SMARCC2_SELENBP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSELENBP1C0001418Adenocarcinoma2CTD_human
TgeneSELENBP1C0036341Schizophrenia2CTD_human
TgeneSELENBP1C0038356Stomach Neoplasms2CTD_human
TgeneSELENBP1C0919267ovarian neoplasm2CTD_human
TgeneSELENBP1C0009404Colorectal Neoplasms1CTD_human
TgeneSELENBP1C0024121Lung Neoplasms1CTD_human
TgeneSELENBP1C0033975Psychotic Disorders1CTD_human
TgeneSELENBP1C4277682Chemical and Drug Induced Liver Injury1CTD_human