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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: 7334

FusionGeneSummary for CLDN11_AASDHPPT

check button Fusion gene summary
Fusion gene informationFusion gene name: CLDN11_AASDHPPT
Fusion gene ID: 7334
HgeneTgene
Gene symbol

CLDN11

AASDHPPT

Gene ID

5010

60496

Gene nameclaudin 11aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase
SynonymsOSP|OTMAASD-PPT|ACPS|CGI-80|LYS2|LYS5
Cytomap

3q26.2

11q22.3

Type of geneprotein-codingprotein-coding
Descriptionclaudin-11oligodendrocyte transmembrane proteinoligodendrocyte-specific proteinL-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase4'-phosphopantetheinyl transferaseLYS5 orthologalpha-aminoadipic semialdehyde dehydrogenase-phosphopantetheinyl transferaseholo ACP synthaseholo-[acyl-carrier-protein] synthase
Modification date2018050620180523
UniProtAcc

O75508

Q9NRN7

Ensembl transtripts involved in fusion geneENST00000486975, ENST00000451576, 
ENST00000064724, ENST00000489485, 
ENST00000278618, 
Fusion gene scores* DoF score5 X 5 X 2=501 X 1 X 1=1
# samples 51
** MAII scorelog2(5/50*10)=0log2(1/1*10)=3.32192809488736
Context

PubMed: CLDN11 [Title/Abstract] AND AASDHPPT [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
ChiTaRS3.1DA211258CLDN11chr3

170232821

+AASDHPPTchr11

105955609

+
* 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-intronENST00000486975ENST00000278618CLDN11chr3

170232821

+AASDHPPTchr11

105955609

+
intron-intronENST00000451576ENST00000278618CLDN11chr3

170232821

+AASDHPPTchr11

105955609

+
intron-intronENST00000064724ENST00000278618CLDN11chr3

170232821

+AASDHPPTchr11

105955609

+
intron-intronENST00000489485ENST00000278618CLDN11chr3

170232821

+AASDHPPTchr11

105955609

+

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FusionProtFeatures for CLDN11_AASDHPPT


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CLDN11

O75508

AASDHPPT

Q9NRN7

Plays a major role in tight junction-specificobliteration of the intercellular space, through calcium-independent cell-adhesion activity. {ECO:0000250}. Catalyzes the post-translational modification of targetproteins by phosphopantetheine. Can transfer the 4'-phosphopantetheine moiety from coenzyme A to a serine residue of abroad range of acceptors, such as the acyl carrier domain of FASN.{ECO:0000269|PubMed:11286508, ECO:0000269|PubMed:12815048,ECO:0000269|PubMed:18022563}.

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 CLDN11_AASDHPPT


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 CLDN11_AASDHPPT


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 CLDN11_AASDHPPT


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 CLDN11_AASDHPPT


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCLDN11C0026769Multiple Sclerosis1CTD_human
HgeneCLDN11C0036341Schizophrenia1PSYGENET