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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: 7196

FusionGeneSummary for CHST8_PDCD5

check button Fusion gene summary
Fusion gene informationFusion gene name: CHST8_PDCD5
Fusion gene ID: 7196
HgeneTgene
Gene symbol

CHST8

PDCD5

Gene ID

64377

9141

Gene namecarbohydrate sulfotransferase 8programmed cell death 5
SynonymsGALNAC4ST1|GalNAc4ST|PSS3TFAR19
Cytomap

19q13.11

19q13.11

Type of geneprotein-codingprotein-coding
Descriptioncarbohydrate sulfotransferase 8GALNAC-4-ST1GalNAc-4-O-sulfotransferase 1N-acetylgalactosamine-4-O-sulfotransferase 1carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 8galNAc4ST-1programmed cell death protein 5TF-1 cell apoptosis-related protein 19TF1 cell apoptosis-related gene 19TFAR19 novel apoptosis-related
Modification date2018051920180523
UniProtAcc

Q9H2A9

O14737

Ensembl transtripts involved in fusion geneENST00000434302, ENST00000438847, 
ENST00000604556, ENST00000262622, 
ENST00000590247, ENST00000419343, 
ENST00000592786, ENST00000379316, 
ENST00000586035, 
Fusion gene scores* DoF score4 X 2 X 4=323 X 1 X 3=9
# samples 43
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: CHST8 [Title/Abstract] AND PDCD5 [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
HgeneCHST8

GO:0006790

sulfur compound metabolic process

11445554

HgeneCHST8

GO:0030166

proteoglycan biosynthetic process

10988300

TgenePDCD5

GO:0010628

positive regulation of gene expression

24012345

TgenePDCD5

GO:0071560

cellular response to transforming growth factor beta stimulus

24012345


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
TCGARVPRADTCGA-EJ-A46G-01ACHST8chr19

34113202

+PDCD5chr19

33073101

+
* 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-3CDSENST00000434302ENST00000590247CHST8chr19

34113202

+PDCD5chr19

33073101

+
5UTR-3CDSENST00000434302ENST00000419343CHST8chr19

34113202

+PDCD5chr19

33073101

+
5UTR-3CDSENST00000434302ENST00000592786CHST8chr19

34113202

+PDCD5chr19

33073101

+
5UTR-3CDSENST00000434302ENST00000379316CHST8chr19

34113202

+PDCD5chr19

33073101

+
5UTR-5UTRENST00000434302ENST00000586035CHST8chr19

34113202

+PDCD5chr19

33073101

+
5UTR-3CDSENST00000438847ENST00000590247CHST8chr19

34113202

+PDCD5chr19

33073101

+
5UTR-3CDSENST00000438847ENST00000419343CHST8chr19

34113202

+PDCD5chr19

33073101

+
5UTR-3CDSENST00000438847ENST00000592786CHST8chr19

34113202

+PDCD5chr19

33073101

+
5UTR-3CDSENST00000438847ENST00000379316CHST8chr19

34113202

+PDCD5chr19

33073101

+
5UTR-5UTRENST00000438847ENST00000586035CHST8chr19

34113202

+PDCD5chr19

33073101

+
3UTR-3CDSENST00000604556ENST00000590247CHST8chr19

34113202

+PDCD5chr19

33073101

+
3UTR-3CDSENST00000604556ENST00000419343CHST8chr19

34113202

+PDCD5chr19

33073101

+
3UTR-3CDSENST00000604556ENST00000592786CHST8chr19

34113202

+PDCD5chr19

33073101

+
3UTR-3CDSENST00000604556ENST00000379316CHST8chr19

34113202

+PDCD5chr19

33073101

+
3UTR-5UTRENST00000604556ENST00000586035CHST8chr19

34113202

+PDCD5chr19

33073101

+
intron-3CDSENST00000262622ENST00000590247CHST8chr19

34113202

+PDCD5chr19

33073101

+
intron-3CDSENST00000262622ENST00000419343CHST8chr19

34113202

+PDCD5chr19

33073101

+
intron-3CDSENST00000262622ENST00000592786CHST8chr19

34113202

+PDCD5chr19

33073101

+
intron-3CDSENST00000262622ENST00000379316CHST8chr19

34113202

+PDCD5chr19

33073101

+
intron-5UTRENST00000262622ENST00000586035CHST8chr19

34113202

+PDCD5chr19

33073101

+

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FusionProtFeatures for CHST8_PDCD5


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CHST8

Q9H2A9

PDCD5

O14737

Catalyzes the transfer of sulfate to position 4 of non-reducing N-acetylgalactosamine (GalNAc) residues in both N-glycansand O-glycans. Required for biosynthesis of glycoprotein hormoneslutropin and thyrotropin, by mediating sulfation of theircarbohydrate structures. Only active against terminalGalNAcbeta1,GalNAcbeta. Not active toward chondroitin.{ECO:0000269|PubMed:10988300, ECO:0000269|PubMed:11445554}. May function in the process of apoptosis.

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 CHST8_PDCD5


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 CHST8_PDCD5


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
CHST8TMED1, CANX, FREM2, C1QBP, FRAS1, TMEM160, P3H4, RBM27, TOR3A, RBM23, CLSTN1, YBEY, ARL10, SEPN1, TMED9, TMED4, TXNDC11, MOXD1, JMJD4, GALNT12, SEC62, GPC6, TMED2, FBL, CHCHD2, MRS2, EDEM2, RRP1, B3GALNT2, GAL3ST1, NOP9, FAM3C, FSTL1PDCD5ACP5, KAT5, KIAA1377, LRIF1, UTP14A, EEF1G, TCEAL1, NUDT3, UBE2D3, FBXW8, TP53, MDM2, FN1, METTL21B, LMNA, KDM1A, VHL, TUBG1, OTUD5, STMN1, CETN2, YAF2, ARRDC5, ATP1B1


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 CHST8_PDCD5


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 CHST8_PDCD5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCHST8C4015729PEELING SKIN SYNDROME 31ORPHANET;UNIPROT