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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: 38502

FusionGeneSummary for TMEM181_SMARCA2

check button Fusion gene summary
Fusion gene informationFusion gene name: TMEM181_SMARCA2
Fusion gene ID: 38502
HgeneTgene
Gene symbol

TMEM181

SMARCA2

Gene ID

57583

6595

Gene nametransmembrane protein 181SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
SynonymsGPR178|KIAA1423BAF190|BRM|NCBRS|SNF2|SNF2L2|SNF2LA|SWI2|Sth1p|hBRM|hSNF2a
Cytomap

6q25.3

9p24.3

Type of geneprotein-codingprotein-coding
Descriptiontransmembrane protein 181G protein-coupled receptor 178probable global transcription activator SNF2L2ATP-dependent helicase SMARCA2BAF190BBRG1-associated factor 190BSNF2-alphaSNF2/SWI2-like protein 2SWI/SNF-related matrix-associated actin-dependent regulator of chromatin a2brahma homologglobal transcr
Modification date2018052320180519
UniProtAcc

Q9P2C4

P51531

Ensembl transtripts involved in fusion geneENST00000367090, ENST00000357248, 
ENST00000349721, ENST00000382203, 
ENST00000382194, ENST00000491574, 
ENST00000324954, ENST00000302401, 
ENST00000382186, ENST00000382185, 
Fusion gene scores* DoF score3 X 3 X 2=1811 X 11 X 5=605
# samples 412
** MAII scorelog2(4/18*10)=1.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(12/605*10)=-2.33390073655344
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TMEM181 [Title/Abstract] AND SMARCA2 [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
TgeneSMARCA2

GO:0008285

negative regulation of cell proliferation

14660596

TgeneSMARCA2

GO:0045892

negative regulation of transcription, DNA-templated

12065415

TgeneSMARCA2

GO:0045893

positive regulation of transcription, DNA-templated

17984088

TgeneSMARCA2

GO:0045944

positive regulation of transcription by RNA polymerase II

15774904


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
ChiTaRS3.1D26155TMEM181chr6

159055150

+SMARCA2chr9

2029019

+
* 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-5UTRENST00000367090ENST00000357248TMEM181chr6

159055150

+SMARCA2chr9

2029019

+
3UTR-5UTRENST00000367090ENST00000349721TMEM181chr6

159055150

+SMARCA2chr9

2029019

+
3UTR-5UTRENST00000367090ENST00000382203TMEM181chr6

159055150

+SMARCA2chr9

2029019

+
3UTR-5UTRENST00000367090ENST00000382194TMEM181chr6

159055150

+SMARCA2chr9

2029019

+
3UTR-intronENST00000367090ENST00000491574TMEM181chr6

159055150

+SMARCA2chr9

2029019

+
3UTR-intronENST00000367090ENST00000324954TMEM181chr6

159055150

+SMARCA2chr9

2029019

+
3UTR-intronENST00000367090ENST00000302401TMEM181chr6

159055150

+SMARCA2chr9

2029019

+
3UTR-intronENST00000367090ENST00000382186TMEM181chr6

159055150

+SMARCA2chr9

2029019

+
3UTR-intronENST00000367090ENST00000382185TMEM181chr6

159055150

+SMARCA2chr9

2029019

+

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FusionProtFeatures for TMEM181_SMARCA2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TMEM181

Q9P2C4

SMARCA2

P51531

Mediates action of cytolethal distending toxins (CDT),which are secreted by many pathogenic bacteria. Expression levelof TMEM181 is rate-limiting for intoxication.{ECO:0000269|PubMed:19965467}. 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. Binds DNA non-specifically(PubMed:22952240, PubMed:26601204). Belongs to the neuralprogenitors-specific chromatin remodeling complex (npBAF complex)and the neuron-specific chromatin remodeling complex (nBAFcomplex). During neural development a switch from astem/progenitor to a postmitotic chromatin remodeling mechanismoccurs as neurons exit the cell cycle and become committed totheir adult state. The transition from proliferating neuralstem/progenitor cells to postmitotic neurons requires a switch insubunit composition of the npBAF and nBAF complexes. As neuralprogenitors exit mitosis and differentiate into neurons, npBAFcomplexes which contain ACTL6A/BAF53A and PHF10/BAF45A, areexchanged for homologous alternative ACTL6B/BAF53B and DPF1/BAF45Bor DPF3/BAF45C subunits in neuron-specific complexes (nBAF). ThenpBAF complex is essential for the self-renewal/proliferativecapacity of the multipotent neural stem cells. The nBAF complexalong with CREST plays a role regulating the activity of genesessential for dendrite growth (By similarity).{ECO:0000250|UniProtKB:Q6DIC0, ECO:0000303|PubMed:22952240,ECO:0000303|PubMed:26601204}.

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 TMEM181_SMARCA2


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 TMEM181_SMARCA2


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 TMEM181_SMARCA2


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 TMEM181_SMARCA2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSMARCA2C0036341Schizophrenia4PSYGENET
TgeneSMARCA2C1303073Nicolaides Baraitser syndrome2CTD_human;ORPHANET;UNIPROT
TgeneSMARCA2C0010606Adenoid Cystic Carcinoma1CTD_human
TgeneSMARCA2C0265338Coffin-Siris syndrome1CTD_human
TgeneSMARCA2C0345967Malignant mesothelioma1CTD_human