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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: 33480

FusionGeneSummary for SFMBT1_PBRM1

check button Fusion gene summary
Fusion gene informationFusion gene name: SFMBT1_PBRM1
Fusion gene ID: 33480
HgeneTgene
Gene symbol

SFMBT1

PBRM1

Gene ID

51460

55193

Gene nameScm like with four mbt domains 1polybromo 1
SynonymsRU1|SFMBT|hSFMBTBAF180|PB1
Cytomap

3p21.1

3p21.1

Type of geneprotein-codingprotein-coding
Descriptionscm-like with four MBT domains protein 1Scm-related gene containing four mbt domainsScm-related gene product containing four mbt domainsrenal ubiquitous protein 1protein polybromo-1BRG1-associated factor 180polybromo-1D
Modification date2018051920180523
UniProtAcc

Q9UHJ3

Q86U86

Ensembl transtripts involved in fusion geneENST00000394752, ENST00000394750, 
ENST00000358080, ENST00000296295, 
ENST00000470575, 
ENST00000356770, 
ENST00000394830, ENST00000296302, 
ENST00000337303, ENST00000410007, 
ENST00000409057, ENST00000409114, 
ENST00000409767, 
Fusion gene scores* DoF score11 X 8 X 8=7045 X 5 X 5=125
# samples 125
** MAII scorelog2(12/704*10)=-2.55254102302878
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/125*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SFMBT1 [Title/Abstract] AND PBRM1 [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
HgeneSFMBT1

GO:0045892

negative regulation of transcription, DNA-templated

23592795


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
TCGALDLIHCTCGA-BC-A10Z-01ASFMBT1chr3

53079832

-PBRM1chr3

52623271

-
* 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
5UTR-3CDSENST00000394752ENST00000356770SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000394752ENST00000394830SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000394752ENST00000296302SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000394752ENST00000337303SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000394752ENST00000410007SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000394752ENST00000409057SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000394752ENST00000409114SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000394752ENST00000409767SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000394750ENST00000356770SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000394750ENST00000394830SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000394750ENST00000296302SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000394750ENST00000337303SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000394750ENST00000410007SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000394750ENST00000409057SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000394750ENST00000409114SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000394750ENST00000409767SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000358080ENST00000356770SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000358080ENST00000394830SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000358080ENST00000296302SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000358080ENST00000337303SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000358080ENST00000410007SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000358080ENST00000409057SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000358080ENST00000409114SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000358080ENST00000409767SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000296295ENST00000356770SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000296295ENST00000394830SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000296295ENST00000296302SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000296295ENST00000337303SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000296295ENST00000410007SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000296295ENST00000409057SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000296295ENST00000409114SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
5UTR-3CDSENST00000296295ENST00000409767SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000470575ENST00000356770SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000470575ENST00000394830SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000470575ENST00000296302SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000470575ENST00000337303SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000470575ENST00000410007SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000470575ENST00000409057SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000470575ENST00000409114SFMBT1chr3

53079832

-PBRM1chr3

52623271

-
intron-3CDSENST00000470575ENST00000409767SFMBT1chr3

53079832

-PBRM1chr3

52623271

-

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FusionProtFeatures for SFMBT1_PBRM1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SFMBT1

Q9UHJ3

PBRM1

Q86U86

Histone-binding protein, which is part of variouscorepressor complexes. Mediates the recruitment of corepressorcomplexes to target genes, followed by chromatin compaction andrepression of transcription. Plays a role during myogenesis:required for the maintenance of undifferentiated states ofmyogenic progenitor cells via interaction with MYOD1. Interactionwith MYOD1 leads to the recruitment of associated corepressors andsilencing of MYOD1 target genes. Part of the SLC complex in germcells, where it may play a role during spermatogenesis.{ECO:0000269|PubMed:17599839, ECO:0000269|PubMed:23349461,ECO:0000269|PubMed:23592795}.

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 SFMBT1_PBRM1


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 SFMBT1_PBRM1


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
SFMBT1PHC1, ACP1, PHC2, HIST1H3A, HIST1H4A, PSMA1, SRPK1, ZCCHC10, CLNK, KIF22, RBPJ, HDAC1, HMG20APBRM1ARID1A, SMARCC2, SMARCC1, SMARCE1, HIST1H3A, HIST1H4A, HIST2H2BE, HIST2H2AC, CHD7, ARID2, SMARCD1, ACTL6A, SMARCB1, SMARCA4, SMARCAD1, HIST3H3, SIRT7, CALML5, APP, GTF3C5, TCHHL1, NOTCH1, MAML1, ZNF512B, HECW2, CDC20, ZDHHC17, OBSL1, EED, DPF3, NUP50, COPS3, BRD7, SCARNA22, IFI16, HIST1H3E, DPPA4, NANOG, POU5F1, TOP1, HDAC6, VHL, BCL7C, BCL7A, ZBTB48, UHRF2, BRD1


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 SFMBT1_PBRM1


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 SFMBT1_PBRM1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePBRM1C0005586Bipolar Disorder3PSYGENET
TgenePBRM1C0007134Renal Cell Carcinoma2CTD_human
TgenePBRM1C0033975Psychotic Disorders1PSYGENET
TgenePBRM1C0036341Schizophrenia1PSYGENET
TgenePBRM1C0040100Thymoma1CTD_human
TgenePBRM1C0206698Cholangiocarcinoma1CTD_human
TgenePBRM1C0349204Nonorganic psychosis1PSYGENET