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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: 14979

FusionGeneSummary for GNL3_CLCN3

check button Fusion gene summary
Fusion gene informationFusion gene name: GNL3_CLCN3
Fusion gene ID: 14979
HgeneTgene
Gene symbol

GNL3

CLCN3

Gene ID

26354

1182

Gene nameG protein nucleolar 3chloride voltage-gated channel 3
SynonymsC77032|E2IG3|NNP47|NSCLC3|ClC-3
Cytomap

3p21.1

4q33

Type of geneprotein-codingprotein-coding
Descriptionguanine nucleotide-binding protein-like 3E2-induced gene 3 proteinestradiol-induced nucleotide binding proteinguanine nucleotide binding protein-like 3 (nucleolar)novel nucleolar protein 47nucleolar GTP-binding protein 3nucleosteminH(+)/Cl(-) exchange transporter 3chloride channel 3chloride channel protein 3chloride channel, voltage-sensitive 3chloride transporter ClC-3
Modification date2018052320180523
UniProtAcc

Q9BVP2

P51790

Ensembl transtripts involved in fusion geneENST00000418458, ENST00000394799, 
ENST00000460073, 
ENST00000513761, 
ENST00000347613, ENST00000360642, 
ENST00000504131, ENST00000506924, 
Fusion gene scores* DoF score7 X 8 X 4=22436 X 4 X 19=2736
# samples 839
** MAII scorelog2(8/224*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(39/2736*10)=-2.81052220113629
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GNL3 [Title/Abstract] AND CLCN3 [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
HgeneGNL3

GO:0017145

stem cell division

25522312

TgeneCLCN3

GO:1902476

chloride transmembrane transport

11274166


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
TCGARVUCECTCGA-E6-A2P8-01AGNL3chr3

52728508

+CLCN3chr4

170623929

+
* 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
5CDS-intronENST00000418458ENST00000513761GNL3chr3

52728508

+CLCN3chr4

170623929

+
5CDS-intronENST00000418458ENST00000347613GNL3chr3

52728508

+CLCN3chr4

170623929

+
5CDS-intronENST00000418458ENST00000360642GNL3chr3

52728508

+CLCN3chr4

170623929

+
5CDS-intronENST00000418458ENST00000504131GNL3chr3

52728508

+CLCN3chr4

170623929

+
5CDS-intronENST00000418458ENST00000506924GNL3chr3

52728508

+CLCN3chr4

170623929

+
5CDS-intronENST00000394799ENST00000513761GNL3chr3

52728508

+CLCN3chr4

170623929

+
5CDS-intronENST00000394799ENST00000347613GNL3chr3

52728508

+CLCN3chr4

170623929

+
5CDS-intronENST00000394799ENST00000360642GNL3chr3

52728508

+CLCN3chr4

170623929

+
5CDS-intronENST00000394799ENST00000504131GNL3chr3

52728508

+CLCN3chr4

170623929

+
5CDS-intronENST00000394799ENST00000506924GNL3chr3

52728508

+CLCN3chr4

170623929

+
intron-intronENST00000460073ENST00000513761GNL3chr3

52728508

+CLCN3chr4

170623929

+
intron-intronENST00000460073ENST00000347613GNL3chr3

52728508

+CLCN3chr4

170623929

+
intron-intronENST00000460073ENST00000360642GNL3chr3

52728508

+CLCN3chr4

170623929

+
intron-intronENST00000460073ENST00000504131GNL3chr3

52728508

+CLCN3chr4

170623929

+
intron-intronENST00000460073ENST00000506924GNL3chr3

52728508

+CLCN3chr4

170623929

+

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FusionProtFeatures for GNL3_CLCN3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GNL3

Q9BVP2

CLCN3

P51790

May be required to maintain the proliferative capacityof stem cells. Stabilizes MDM2 by preventing its ubiquitination,and hence proteasomal degradation (By similarity). {ECO:0000250,ECO:0000269|PubMed:12464630, ECO:0000269|PubMed:16012751}. Mediates the exchange of chloride ions against protons.Functions as antiporter and contributes to the acidification ofthe endosome and synaptic vesicle lumen, and may thereby affectvesicle trafficking and exocytosis. May play an important role inneuronal cell function through regulation of membrane excitabilityby protein kinase C. It could help neuronal cells to establishshort-term memory. {ECO:0000269|PubMed:11967229}.

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 GNL3_CLCN3


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 GNL3_CLCN3


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
GNL3ASCC2, TP53, MDM2, DOT1L, TERF1, NOP56, OAS3, EIF2AK2, HDGF, SIRT7, CUL3, CUL1, COPS5, CAND1, RPL11, RPL6, RPS7, RPL18A, RPL7, RPL15, FBL, RPL23, RPS15A, RPL37A, EBNA1BP2, RPS6, RPL19, RPL4, RPS4X, RPS5, RPS3, RPL5, NHP2L1, RPS8, RPS24, NOP58, RPS14, EIF6, EIF4A3, RNPS1, RRP7A, NOP2, RRS1, NIFK, FTSJ3, BCCIP, RPLP0P6, DIDO1, BOP1, ESR1, MPG, STAT3, SRPK3, TARDBP, CDKN2A, TRIP12, CUL7, OBSL1, EED, RNF2, NTRK1, DDX24, DKC1, KIAA0020, KRR1, PES1, RBBP4, RBBP7, TEX10, RPL14, SCARNA22, IFI16, CEP19, HNRNPU, NPM1, RPL10, ZNF746, RPL18, PPAN, NCL, CDKN1B, INO80B, DLST, PDHA1, TRIM25, MTF1CLCN3CLCN3, SLC9A3R1, PDZK1, GOPC, CFTR, LGALS3, LGALS8, LGALS9, LYPD3, HSPB1, TMEM9B, GGA1, TPCN2, TRIM25


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 GNL3_CLCN3


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 GNL3_CLCN3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneCLCN3C0017638Glioma1CTD_human
TgeneCLCN3C0038356Stomach Neoplasms1CTD_human
TgeneCLCN3C2931822Nasopharyngeal carcinoma1CTD_human