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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: 27138

FusionGeneSummary for PIGM_ZBTB7C

check button Fusion gene summary
Fusion gene informationFusion gene name: PIGM_ZBTB7C
Fusion gene ID: 27138
HgeneTgene
Gene symbol

PIGM

ZBTB7C

Gene ID

93183

201501

Gene namephosphatidylinositol glycan anchor biosynthesis class Mzinc finger and BTB domain containing 7C
SynonymsGPI-MT-IAPM-1|APM1|ZBTB36|ZNF857C
Cytomap

1q23.2

18q21.1

Type of geneprotein-codingprotein-coding
DescriptionGPI mannosyltransferase 1DPM:GlcN-(acyl-)PI mannosyltransferaseGPI mannosyltransferase IPIG-M mannosyltransferasedol-P-Man dependent GPI mannosyltransferasephosphatidylinositol-glycan biosynthesis class M proteinzinc finger and BTB domain-containing protein 7CB230208J24Rikaffected by papillomavirus DNA integration in ME180 cells protein 1zinc finger and BTB domain containing 36zinc finger and BTB domain-containing protein 36zinc finger protein 857C
Modification date2018052220180519
UniProtAcc

Q9H3S5

A1YPR0

Ensembl transtripts involved in fusion geneENST00000368090, ENST00000535628, 
ENST00000588982, ENST00000586438, 
ENST00000590800, ENST00000332053, 
Fusion gene scores* DoF score1 X 1 X 1=17 X 6 X 5=210
# samples 18
** MAII scorelog2(1/1*10)=3.32192809488736log2(8/210*10)=-1.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PIGM [Title/Abstract] AND ZBTB7C [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
TgeneZBTB7C

GO:0008285

negative regulation of cell proliferation

9427755


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
ChiTaRS3.1BE843437PIGMchr1

160000558

-ZBTB7Cchr18

45853369

-
* 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-intronENST00000368090ENST00000535628PIGMchr1

160000558

-ZBTB7Cchr18

45853369

-
intron-intronENST00000368090ENST00000588982PIGMchr1

160000558

-ZBTB7Cchr18

45853369

-
intron-intronENST00000368090ENST00000586438PIGMchr1

160000558

-ZBTB7Cchr18

45853369

-
intron-intronENST00000368090ENST00000590800PIGMchr1

160000558

-ZBTB7Cchr18

45853369

-
intron-intronENST00000368090ENST00000332053PIGMchr1

160000558

-ZBTB7Cchr18

45853369

-

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FusionProtFeatures for PIGM_ZBTB7C


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

Q9H3S5

ZBTB7C

A1YPR0

Mannosyltransferase involved inglycosylphosphatidylinositol-anchor biosynthesis. Transfers thefirst alpha-1,4-mannose to GlcN-acyl-PI during GPI precursorassembly. {ECO:0000269|PubMed:11226175}. May be a tumor suppressor gene.{ECO:0000269|PubMed:9427755}.

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 PIGM_ZBTB7C


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 PIGM_ZBTB7C


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 PIGM_ZBTB7C


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 PIGM_ZBTB7C


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePIGMC0036572Seizures1CTD_human
HgenePIGMC0042487Venous Thrombosis1CTD_human