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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: 31838

FusionGeneSummary for RPL23AP53_SDCCAG8

check button Fusion gene summary
Fusion gene informationFusion gene name: RPL23AP53_SDCCAG8
Fusion gene ID: 31838
HgeneTgene
Gene symbol

RPL23AP53

SDCCAG8

Gene ID

644128

10806

Gene nameribosomal protein L23a pseudogene 53serologically defined colon cancer antigen 8
SynonymsRPL23A_20_869BBS16|CCCAP|CCCAP SLSN7|HSPC085|NPHP10|NY-CO-8|SLSN7|hCCCAP
Cytomap

8p23.3

1q43-q44

Type of genepseudoprotein-coding
Description-serologically defined colon cancer antigen 8Bardet-Biedl syndrome 16antigen NY-CO-8centrosomal colon cancer autoantigen proteinnephrocystin 10
Modification date2018032920180523
UniProtAcc

Q86SQ7

Ensembl transtripts involved in fusion geneENST00000606975, ENST00000355875, 
ENST00000366541, ENST00000343783, 
ENST00000391846, ENST00000496361, 
Fusion gene scores* DoF score2 X 2 X 1=413 X 10 X 7=910
# samples 313
** MAII scorelog2(3/4*10)=2.90689059560852log2(13/910*10)=-2.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RPL23AP53 [Title/Abstract] AND SDCCAG8 [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
ChiTaRS3.1BF762716RPL23AP53chr8

169820

-SDCCAG8chr1

243529496

+
* 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-intronENST00000606975ENST00000355875RPL23AP53chr8

169820

-SDCCAG8chr1

243529496

+
intron-intronENST00000606975ENST00000366541RPL23AP53chr8

169820

-SDCCAG8chr1

243529496

+
intron-intronENST00000606975ENST00000343783RPL23AP53chr8

169820

-SDCCAG8chr1

243529496

+
intron-intronENST00000606975ENST00000391846RPL23AP53chr8

169820

-SDCCAG8chr1

243529496

+
intron-intronENST00000606975ENST00000496361RPL23AP53chr8

169820

-SDCCAG8chr1

243529496

+

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FusionProtFeatures for RPL23AP53_SDCCAG8


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RPL23AP53

SDCCAG8

Q86SQ7

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}. Plays a role in the establishment of cell polarity andepithelial lumen formation (By similarity). May play a role inciliogenesis. {ECO:0000250|UniProtKB:Q80UF4}.

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 RPL23AP53_SDCCAG8


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 RPL23AP53_SDCCAG8


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 RPL23AP53_SDCCAG8


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 RPL23AP53_SDCCAG8


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSDCCAG8C0035309Retinal Diseases1CTD_human
TgeneSDCCAG8C0036341Schizophrenia1PSYGENET
TgeneSDCCAG8C1691228Cystic Kidney Diseases1CTD_human