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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: 39689

FusionGeneSummary for TRPS1_PCGF5

check button Fusion gene summary
Fusion gene informationFusion gene name: TRPS1_PCGF5
Fusion gene ID: 39689
HgeneTgene
Gene symbol

TRPS1

PCGF5

Gene ID

7227

84333

Gene nametranscriptional repressor GATA binding 1polycomb group ring finger 5
SynonymsGC79|LGCRRNF159
Cytomap

8q23.3

10q23.32

Type of geneprotein-codingprotein-coding
Descriptionzinc finger transcription factor Trps1tricho-rhino-phalangeal syndrome type I proteintrichorhinophalangeal syndrome Izinc finger protein GC79polycomb group RING finger protein 5RING finger protein 159ring finger protein (C3HC4 type) 159
Modification date2018051920180523
UniProtAcc

Q9UHF7

Q86SE9

Ensembl transtripts involved in fusion geneENST00000395715, ENST00000220888, 
ENST00000519076, ENST00000520276, 
ENST00000519674, 
ENST00000371687, 
ENST00000543648, ENST00000490164, 
ENST00000336126, 
Fusion gene scores* DoF score14 X 6 X 3=2523 X 4 X 2=24
# samples 134
** MAII scorelog2(13/252*10)=-0.954912110471462
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/24*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TRPS1 [Title/Abstract] AND PCGF5 [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
HgeneTRPS1

GO:0000122

negative regulation of transcription by RNA polymerase II

12885770|21673316

TgenePCGF5

GO:0045944

positive regulation of transcription by RNA polymerase II

25519132


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
ChiTaRS3.1BF329822TRPS1chr8

116454627

+PCGF5chr10

93002873

+
* 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-intronENST00000395715ENST00000371687TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000395715ENST00000543648TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000395715ENST00000490164TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000395715ENST00000336126TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000220888ENST00000371687TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000220888ENST00000543648TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000220888ENST00000490164TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000220888ENST00000336126TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000519076ENST00000371687TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000519076ENST00000543648TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000519076ENST00000490164TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000519076ENST00000336126TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000520276ENST00000371687TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000520276ENST00000543648TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000520276ENST00000490164TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000520276ENST00000336126TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000519674ENST00000371687TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000519674ENST00000543648TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000519674ENST00000490164TRPS1chr8

116454627

+PCGF5chr10

93002873

+
intron-intronENST00000519674ENST00000336126TRPS1chr8

116454627

+PCGF5chr10

93002873

+

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FusionProtFeatures for TRPS1_PCGF5


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TRPS1

Q9UHF7

PCGF5

Q86SE9

Transcriptional repressor. Binds specifically to GATAsequences and represses expression of GATA-regulated genes atselected sites and stages in vertebrate development. Regulateschondrocyte proliferation and differentiation. Executes multiplefunctions in proliferating chondrocytes, expanding the region ofdistal chondrocytes, activating proliferation in columnar cellsand supporting the differentiation of columnar into hypertrophicchondrocytes. {ECO:0000269|PubMed:12885770,ECO:0000269|PubMed:17391059}. Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain thetranscriptionally repressive state of many genes, including Hoxgenes, throughout development. PcG PRC1 complex acts via chromatinremodeling and modification of histones; it mediatesmonoubiquitination of histone H2A 'Lys-119', rendering chromatinheritably changed in its expressibility (PubMed:26151332). Withinthe PRC1-like complex, regulates RNF2 ubiquitin ligase activity(PubMed:26151332). Plays a redundant role with PCGF3 as part of aPRC1-like complex that mediates monoubiquitination of histone H2A'Lys-119' on the X chromosome and is required for normal silencingof one copy of the X chromosome in XX females (By similarity).{ECO:0000250|UniProtKB:Q3UK78, ECO:0000269|PubMed:26151332}.

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 TRPS1_PCGF5


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 TRPS1_PCGF5


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 TRPS1_PCGF5


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 TRPS1_PCGF5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTRPS1C0376634Craniofacial Abnormalities2CTD_human
HgeneTRPS1C1860823Trichorhinophalangeal Syndrome, Type III2CTD_human;UNIPROT
HgeneTRPS1C0005941Bone Diseases, Developmental1CTD_human
HgeneTRPS1C0023003Langer-Giedion Syndrome1CTD_human;ORPHANET
HgeneTRPS1C0024667Animal Mammary Neoplasms1CTD_human
HgeneTRPS1C0024668Mammary Neoplasms, Experimental1CTD_human
HgeneTRPS1C0432233Trichorhinophalangeal dysplasia type I1CTD_human;UNIPROT