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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: 33577

FusionGeneSummary for SGMS1_PSMB2

check button Fusion gene summary
Fusion gene informationFusion gene name: SGMS1_PSMB2
Fusion gene ID: 33577
HgeneTgene
Gene symbol

SGMS1

PSMB2

Gene ID

259230

5690

Gene namesphingomyelin synthase 1proteasome subunit beta 2
SynonymsMOB|MOB1|SMS1|TMEM23|hmob33HC7-I
Cytomap

10q11.23

1p34.3

Type of geneprotein-codingprotein-coding
Descriptionphosphatidylcholine:ceramide cholinephosphotransferase 1medulla oblongata-derived proteinprotein Mobtransmembrane protein 23proteasome subunit beta type-2macropain subunit C7-Imulticatalytic endopeptidase complex subunit C7-1multicatalytic endopeptidase complex subunit C7-Iproteasome (prosome, macropain) subunit, beta type, 2proteasome beta 2 subunitproteasome component
Modification date2018052320180523
UniProtAcc

Q86VZ5

P49721

Ensembl transtripts involved in fusion geneENST00000361781, ENST00000429490, 
ENST00000492601, ENST00000361543, 
ENST00000373237, 
Fusion gene scores* DoF score7 X 4 X 6=1685 X 4 X 3=60
# samples 76
** MAII scorelog2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/60*10)=0
Context

PubMed: SGMS1 [Title/Abstract] AND PSMB2 [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
HgeneSGMS1

GO:0006686

sphingomyelin biosynthetic process

14685263|14976195

HgeneSGMS1

GO:0046513

ceramide biosynthetic process

25605874


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
TCGALDBRCATCGA-EW-A1OV-01ASGMS1chr10

52193236

-PSMB2chr1

36102033

-
* 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-3CDSENST00000361781ENST00000373237SGMS1chr10

52193236

-PSMB2chr1

36102033

-
intron-3CDSENST00000429490ENST00000373237SGMS1chr10

52193236

-PSMB2chr1

36102033

-
intron-3CDSENST00000492601ENST00000373237SGMS1chr10

52193236

-PSMB2chr1

36102033

-
intron-3CDSENST00000361543ENST00000373237SGMS1chr10

52193236

-PSMB2chr1

36102033

-

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FusionProtFeatures for SGMS1_PSMB2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SGMS1

Q86VZ5

PSMB2

P49721

Sphingomyelin synthases synthesize the sphingolipid,sphingomyelin, through transfer of the phosphatidyl head group,phosphatidylcholine, on to the primary hydroxyl of ceramide. Thereaction is bidirectional depending on the respective levels ofthe sphingolipid and ceramide. Golgi apparatus SMS1 directly andspecifically recognizes the choline head group on the substrate,requiring two fatty chains on the choline-P donor molecule inorder to be recognized efficiently as a substrate. Major form inmacrophages. Required for cell growth in certain cell types suchas HeLa cells. Suppresses BAX-mediated apoptosis and also preventscell death in response to stimuli such as hydrogen peroxide,osmotic stress, elevated temperature and exogenously suppliedsphingolipids. May protect against cell death by reversing thestress-inducible increase in levels of proapoptotic ceramide.{ECO:0000269|PubMed:14685263, ECO:0000269|PubMed:17449912}. Component of the 20S core proteasome complex involved inthe proteolytic degradation of most intracellular proteins. Thiscomplex plays numerous essential roles within the cell byassociating with different regulatory particles. Associated withtwo 19S regulatory particles, forms the 26S proteasome and thusparticipates in the ATP-dependent degradation of ubiquitinatedproteins. The 26S proteasome plays a key role in the maintenanceof protein homeostasis by removing misfolded or damaged proteinsthat could impair cellular functions, and by removing proteinswhose functions are no longer required. Associated with the PA200or PA28, the 20S proteasome mediates ubiquitin-independent proteindegradation. This type of proteolysis is required in severalpathways including spermatogenesis (20S-PA200 complex) orgeneration of a subset of MHC class I-presented antigenic peptides(20S-PA28 complex). {ECO:0000269|PubMed:15244466,ECO:0000269|PubMed:27176742, ECO:0000269|PubMed:8610016}.

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 SGMS1_PSMB2


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 SGMS1_PSMB2


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
SGMS1ATXN1, STK4, PTAR1, TRIM25PSMB2SLX1B, UBC, PSMA2, RAD23A, PSMA1, PSMB3, FKBP8, UCHL5, POMP, PSMB1, PSMB5, PSMB7, PSMA3, PSMA4, PSMA5, PSMA6, PSMA7, PSMB4, PSMB6, PSMB8, PSMC6, PSMC1, PSMC4, PSMC2, PSMC5, PSMD11, PSMD7, PSMD1, PSMD2, PSMD8, PSMD6, PSMC3, PSMD12, PSMD13, PSMD3, PSMD14, PSMD4, PSME1, PSMD5, PSME3, PSMA8, UBA52, RAD23B, TST, UBE2A, PYGB, FOLR1, YBX1, HRAS, SMARCA2, TUBB, C11orf58, PIR, UBE2B, SEC23A, VIM, SULT1A4, FN1, VCAM1, IQCB1, ITGA4, PARK2, GPX2, DDX49, CDK20, HOXA2, PYCRL, ASB11, KRT13, KCTD9, AMFR, SYVN1, PSMB9, HSPB1, AMBRA1, ACACA, ASNA1, ADRM1, MRPS9, PGK1, YWHAE, XPOT, PTEN, MCM2, POU5F1, UBLCP1, PSME4, AKIRIN2, PSMG2, PSME2, PSMF1, FBXO7, PSMG1, CYLD


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 SGMS1_PSMB2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgenePSMB2P49721DB08889CarfilzomibProteasome subunit beta type-2small moleculeapproved|investigational

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RelatedDiseases for SGMS1_PSMB2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePSMB2C0005695Bladder Neoplasm1CTD_human