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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: 7346

FusionGeneSummary for CLDN1_PARD3

check button Fusion gene summary
Fusion gene informationFusion gene name: CLDN1_PARD3
Fusion gene ID: 7346
HgeneTgene
Gene symbol

CLDN1

PARD3

Gene ID

9076

56288

Gene nameclaudin 1par-3 family cell polarity regulator
SynonymsCLD1|ILVASC|SEMP1ASIP|Baz|PAR3|PAR3alpha|PARD-3|PARD3A|PPP1R118|SE2-5L16|SE2-5LT1|SE2-5T2
Cytomap

3q28

10p11.22-p11.21

Type of geneprotein-codingprotein-coding
Descriptionclaudin-1senescence-associated epithelial membrane protein 1partitioning defective 3 homologCTCL tumor antigen se2-5PAR3-alphaatypical PKC isotype-specific interacting proteinbazookapar-3 family cell polarity regulator alphapar-3 partitioning defective 3 homologprotein phosphatase 1, regulatory subunit 118
Modification date2018051920180523
UniProtAcc

O95832

Q8TEW0

Ensembl transtripts involved in fusion geneENST00000295522, ENST00000545260, 
ENST00000545693, ENST00000350537, 
ENST00000346874, ENST00000374789, 
ENST00000374790, ENST00000374794, 
ENST00000374788, ENST00000466092, 
ENST00000374776, ENST00000340077, 
ENST00000544292, ENST00000374773, 
ENST00000374768, 
Fusion gene scores* DoF score2 X 2 X 1=49 X 10 X 4=360
# samples 412
** MAII scorelog2(4/4*10)=3.32192809488736log2(12/360*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CLDN1 [Title/Abstract] AND PARD3 [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
ChiTaRS3.1BQ022914CLDN1chr3

190025563

+PARD3chr10

35084174

+
ChiTaRS3.1BQ025642CLDN1chr3

190025563

+PARD3chr10

35084174

+
ChiTaRS3.1BU753063CLDN1chr3

190025563

+PARD3chr10

35084174

+
* 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-intronENST00000295522ENST00000545260CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000545693CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000350537CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000346874CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000374789CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000374790CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000374794CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000374788CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000466092CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000374776CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000340077CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000544292CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000374773CLDN1chr3

190025563

+PARD3chr10

35084174

+
intron-intronENST00000295522ENST00000374768CLDN1chr3

190025563

+PARD3chr10

35084174

+

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FusionProtFeatures for CLDN1_PARD3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CLDN1

O95832

PARD3

Q8TEW0

Claudins function as major constituents of the tightjunction complexes that regulate the permeability of epithelia.While some claudin family members play essential roles in theformation of impermeable barriers, others mediate the permeabilityto ions and small molecules. Often, several claudin family membersare coexpressed and interact with each other, and this determinesthe overall permeability. CLDN1 is required to prevent theparacellular diffusion of small molecules through tight junctionsin the epidermis and is required for the normal barrier functionof the skin. Required for normal water homeostasis and to preventexcessive water loss through the skin, probably via an indirecteffect on the expression levels of other proteins, since CLDN1itself seems to be dispensable for water barrier formation inkeratinocyte tight junctions (PubMed:23407391).{ECO:0000269|PubMed:23407391}. (Microbial infection) Acts as a receptor for hepatitis Cvirus (HCV) in hepatocytes (PubMed:17325668, PubMed:20375010).Associates with CD81 and the CLDN1-CD81 receptor complex isessential for HCV entry into host cell (PubMed:20375010). Acts asa receptor for dengue virus (PubMed:24074594).{ECO:0000269|PubMed:17325668, ECO:0000269|PubMed:20375010,ECO:0000269|PubMed:24074594}.

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 CLDN1_PARD3


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 CLDN1_PARD3


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 CLDN1_PARD3


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 CLDN1_PARD3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCLDN1C1458155Mammary Neoplasms2CTD_human
HgeneCLDN1C0007621Neoplastic Cell Transformation1CTD_human
HgeneCLDN1C0011616Contact Dermatitis1CTD_human
HgeneCLDN1C0014175Endometriosis1CTD_human