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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: 42947

FusionGeneSummary for ZMPSTE24_SMAP2

check button Fusion gene summary
Fusion gene informationFusion gene name: ZMPSTE24_SMAP2
Fusion gene ID: 42947
HgeneTgene
Gene symbol

ZMPSTE24

SMAP2

Gene ID

10269

64744

Gene namezinc metallopeptidase STE24small ArfGAP2
SynonymsFACE-1|FACE1|HGPS|PRO1|STE24|Ste24pSMAP1L
Cytomap

1p34.2

1p34.2

Type of geneprotein-codingprotein-coding
DescriptionCAAX prenyl protease 1 homologfarnesylated proteins-converting enzyme 1prenyl protein-specific endoprotease 1zinc metallopeptidase STE24 homologzinc metalloproteinase Ste24 homologstromal membrane-associated protein 2stromal membrane-associated GTPase-activating protein 2
Modification date2018052320180522
UniProtAcc

O75844

Q8WU79

Ensembl transtripts involved in fusion geneENST00000372759, ENST00000479131, 
ENST00000539317, ENST00000487871, 
Fusion gene scores* DoF score5 X 3 X 5=755 X 5 X 3=75
# samples 65
** MAII scorelog2(6/75*10)=-0.321928094887362
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZMPSTE24 [Title/Abstract] AND SMAP2 [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
TCGALDBLCATCGA-FD-A62S-01AZMPSTE24chr1

40737707

+SMAP2chr1

40872408

+
* 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
5CDS-5UTRENST00000372759ENST00000539317ZMPSTE24chr1

40737707

+SMAP2chr1

40872408

+
5CDS-intronENST00000372759ENST00000487871ZMPSTE24chr1

40737707

+SMAP2chr1

40872408

+
intron-5UTRENST00000479131ENST00000539317ZMPSTE24chr1

40737707

+SMAP2chr1

40872408

+
intron-intronENST00000479131ENST00000487871ZMPSTE24chr1

40737707

+SMAP2chr1

40872408

+

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FusionProtFeatures for ZMPSTE24_SMAP2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ZMPSTE24

O75844

SMAP2

Q8WU79

Proteolytically removes the C-terminal three residues offarnesylated proteins. Acts on lamin A/C.

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 ZMPSTE24_SMAP2


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 ZMPSTE24_SMAP2


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
ZMPSTE24MME, ELAVL1, DDOST, S100A10, MGST3, ATP6V1H, NDUFB7, TMEM43, UQCRFS1P1, SYNJ2BP, RAB5C, GALNT2, HNRNPF, CD55, MRPS5, VDAC1, HNRNPUL1, KIAA2013, PTPN1, MRPL40, RAB10, BAG3, PMF1, RNF26, CYP1A1, CLTC, TCTN2, TCTN3, SLC18A1, TNFRSF17, GDPD5, VAC14, FDPS, MED21, DEFB4A, GPR21, GTF2E2, SLC17A2, TMPRSS12, SLC2A5, DUSP23, GJB7SMAP2FN1, VCAM1, DAB1, MAGED1, DAZAP2, FAM168A, C1orf94, SLC25A11, SLC2A4, CRYZ, CEP170, CNTROB, TMEM17, XPO1, GTSE1, MFSD4, SLC22A12, CLINT1, CELF5, STAMBPL1, MFSD11, CDIPT, SLC5A8, SLC2A14, SLC2A12, RBMS1, SMAD9, ZNF143


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 ZMPSTE24_SMAP2


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 ZMPSTE24_SMAP2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneZMPSTE24C1837756MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY3CTD_human;ORPHANET;UNIPROT
HgeneZMPSTE24C0917990Acro-Osteolysis2CTD_human
HgeneZMPSTE24C0017668Focal glomerulosclerosis1CTD_human
HgeneZMPSTE24C0023787Lipodystrophy1CTD_human
HgeneZMPSTE24C0024689Mandibular Diseases1CTD_human
HgeneZMPSTE24C0033300Progeria1CTD_human;ORPHANET
HgeneZMPSTE24C0376634Craniofacial Abnormalities1CTD_human
HgeneZMPSTE24C1136321HIV-Associated Lipodystrophy Syndrome1CTD_human