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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: 7326

FusionGeneSummary for CLCN5_CLCN5

check button Fusion gene summary
Fusion gene informationFusion gene name: CLCN5_CLCN5
Fusion gene ID: 7326
HgeneTgene
Gene symbol

CLCN5

CLCN5

Gene ID

1184

1184

Gene namechloride voltage-gated channel 5chloride voltage-gated channel 5
SynonymsCLC5|CLCK2|ClC-5|DENTS|NPHL1|NPHL2|XLRH|XRN|hCIC-K2CLC5|CLCK2|ClC-5|DENTS|NPHL1|NPHL2|XLRH|XRN|hCIC-K2
Cytomap

Xp11.23

Xp11.23

Type of geneprotein-codingprotein-coding
DescriptionH(+)/Cl(-) exchange transporter 5chloride channel, voltage-sensitive 5chloride transporter ClC-5voltage-gated chloride ion channel CLCN5H(+)/Cl(-) exchange transporter 5chloride channel, voltage-sensitive 5chloride transporter ClC-5voltage-gated chloride ion channel CLCN5
Modification date2018052320180523
UniProtAcc

P51795

P51795

Ensembl transtripts involved in fusion geneENST00000376088, ENST00000376091, 
ENST00000482218, ENST00000376108, 
ENST00000307367, 
ENST00000376088, 
ENST00000376091, ENST00000482218, 
ENST00000376108, ENST00000307367, 
Fusion gene scores* DoF score2 X 2 X 2=82 X 2 X 2=8
# samples 22
** MAII scorelog2(2/8*10)=1.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: CLCN5 [Title/Abstract] AND CLCN5 [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
ChiTaRS3.1EB386816CLCN5chrX

49843306

-CLCN5chrX

49860503

-
* 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-3UTRENST00000376088ENST00000376088CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376088ENST00000376091CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376088ENST00000482218CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376088ENST00000376108CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376088ENST00000307367CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-3UTRENST00000376091ENST00000376088CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376091ENST00000376091CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376091ENST00000482218CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376091ENST00000376108CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376091ENST00000307367CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-3UTRENST00000482218ENST00000376088CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000482218ENST00000376091CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000482218ENST00000482218CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000482218ENST00000376108CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000482218ENST00000307367CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-3UTRENST00000376108ENST00000376088CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376108ENST00000376091CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376108ENST00000482218CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376108ENST00000376108CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000376108ENST00000307367CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-3UTRENST00000307367ENST00000376088CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000307367ENST00000376091CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000307367ENST00000482218CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000307367ENST00000376108CLCN5chrX

49843306

-CLCN5chrX

49860503

-
intron-intronENST00000307367ENST00000307367CLCN5chrX

49843306

-CLCN5chrX

49860503

-

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FusionProtFeatures for CLCN5_CLCN5


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CLCN5

P51795

CLCN5

P51795

Proton-coupled chloride transporter. Functions asantiport system and exchanges chloride ions against protons.Important for normal acidification of the endosome lumen. May playan important role in renal tubular function. Proton-coupled chloride transporter. Functions asantiport system and exchanges chloride ions against protons.Important for normal acidification of the endosome lumen. May playan important role in renal tubular function.

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 CLCN5_CLCN5


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 CLCN5_CLCN5


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 CLCN5_CLCN5


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 CLCN5_CLCN5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCLCN5C1848336Dent disease 112CTD_human;ORPHANET;UNIPROT
HgeneCLCN5C1845168Hypophosphatemic Rickets, X-Linked Recessive6UNIPROT
HgeneCLCN5C0878681Dent's disease3CTD_human
HgeneCLCN5C1839874Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis3CTD_human;UNIPROT
HgeneCLCN5C0017638Glioma1CTD_human
HgeneCLCN5C0018021Goiter1CTD_human
HgeneCLCN5C0033687Proteinuria1CTD_human
HgeneCLCN5C0403720X-linked recessive nephrolithiasis with renal failure1CTD_human;UNIPROT
TgeneCLCN5C1848336Dent disease 112CTD_human;ORPHANET;UNIPROT
TgeneCLCN5C1845168Hypophosphatemic Rickets, X-Linked Recessive6UNIPROT
TgeneCLCN5C0878681Dent's disease3CTD_human
TgeneCLCN5C1839874Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis3CTD_human;UNIPROT
TgeneCLCN5C0017638Glioma1CTD_human
TgeneCLCN5C0018021Goiter1CTD_human
TgeneCLCN5C0033687Proteinuria1CTD_human
TgeneCLCN5C0403720X-linked recessive nephrolithiasis with renal failure1CTD_human;UNIPROT