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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: 7191

FusionGeneSummary for CHST3_CDH23

check button Fusion gene summary
Fusion gene informationFusion gene name: CHST3_CDH23
Fusion gene ID: 7191
HgeneTgene
Gene symbol

CHST3

CDH23

Gene ID

9469

64072

Gene namecarbohydrate sulfotransferase 3cadherin related 23
SynonymsC6ST|C6ST1|HSDCDHR23|PITA5|USH1D
Cytomap

10q22.1

10q22.1

Type of geneprotein-codingprotein-coding
Descriptioncarbohydrate sulfotransferase 3C6ST-1GST-0carbohydrate (chondroitin 6) sulfotransferase 3chondroitin 6 sulfotransferase 1chondroitin 6-O-sulfotransferase 1galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 0cadherin-23cadherin-like 23cadherin-related family member 23otocadherin
Modification date2018052320180519
UniProtAcc

Q7LGC8

Q9H251

Ensembl transtripts involved in fusion geneENST00000373115, ENST00000398842, 
ENST00000398809, ENST00000461841, 
ENST00000299366, ENST00000224721, 
ENST00000398788, ENST00000475158, 
Fusion gene scores* DoF score1 X 1 X 1=110 X 7 X 5=350
# samples 110
** MAII scorelog2(1/1*10)=3.32192809488736log2(10/350*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CHST3 [Title/Abstract] AND CDH23 [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
HgeneCHST3

GO:0006790

sulfur compound metabolic process

9883891

HgeneCHST3

GO:0030206

chondroitin sulfate biosynthetic process

9883891


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
TCGARVLUADTCGA-78-8662-01ACHST3chr10

73724452

+CDH23chr10

73571072

+
* 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-intronENST00000373115ENST00000398842CHST3chr10

73724452

+CDH23chr10

73571072

+
5UTR-intronENST00000373115ENST00000398809CHST3chr10

73724452

+CDH23chr10

73571072

+
5UTR-intronENST00000373115ENST00000461841CHST3chr10

73724452

+CDH23chr10

73571072

+
5UTR-intronENST00000373115ENST00000299366CHST3chr10

73724452

+CDH23chr10

73571072

+
5UTR-intronENST00000373115ENST00000224721CHST3chr10

73724452

+CDH23chr10

73571072

+
5UTR-intronENST00000373115ENST00000398788CHST3chr10

73724452

+CDH23chr10

73571072

+
5UTR-3UTRENST00000373115ENST00000475158CHST3chr10

73724452

+CDH23chr10

73571072

+

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FusionProtFeatures for CHST3_CDH23


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CHST3

Q7LGC8

CDH23

Q9H251

Sulfotransferase that utilizes 3'-phospho-5'-adenylylsulfate (PAPS) as sulfonate donor to catalyze the transfer ofsulfate to position 6 of the N-acetylgalactosamine (GalNAc)residue of chondroitin. Chondroitin sulfate constitutes thepredominant proteoglycan present in cartilage and is distributedon the surfaces of many cells and extracellular matrices. Can alsosulfate Gal residues of keratan sulfate, anotherglycosaminoglycan, and the Gal residues in sialyl N-acetyllactosamine (sialyl LacNAc) oligosaccharides. May play arole in the maintenance of naive T-lymphocytes in the spleen.{ECO:0000269|PubMed:9714738, ECO:0000269|PubMed:9883891}.

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 CHST3_CDH23


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 CHST3_CDH23


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
CHST3ELAVL1, CRP, SCGB2A2, PTCH1, AVP, OFD1CDH23USH1C, LYN, CLK1, PPME1, GOPC, NCKAP1, ABI1, NXN, WASF1, CYFIP1, SLC9A3R2


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 CHST3_CDH23


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 CHST3_CDH23


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCHST3C1837657Spondyloepiphyseal dysplasia, Omani type2CTD_human;ORPHANET;UNIPROT
TgeneCDH23C1832394Deafness, Autosomal Recessive 128CTD_human;UNIPROT
TgeneCDH23C1832845USHER SYNDROME, TYPE ID6UNIPROT
TgeneCDH23C0032273Pneumoconiosis1CTD_human