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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: 26085

FusionGeneSummary for PAX8_GLIS1

check button Fusion gene summary
Fusion gene informationFusion gene name: PAX8_GLIS1
Fusion gene ID: 26085
HgeneTgene
Gene symbol

PAX8

GLIS1

Gene ID

7849

148979

Gene namepaired box 8GLIS family zinc finger 1
Synonyms--
Cytomap

2q14.1

1p32.3

Type of geneprotein-codingprotein-coding
Descriptionpaired box protein Pax-8paired domain gene 8zinc finger protein GLIS1GLI-similar 1
Modification date2018051920180403
UniProtAcc

Q06710

Q8NBF1

Ensembl transtripts involved in fusion geneENST00000348715, ENST00000397647, 
ENST00000263335, ENST00000429538, 
ENST00000263334, 
ENST00000312233, 
Fusion gene scores* DoF score7 X 8 X 4=2247 X 5 X 5=175
# samples 138
** MAII scorelog2(13/224*10)=-0.784987109029149
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/175*10)=-1.12928301694497
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PAX8 [Title/Abstract] AND GLIS1 [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
HgenePAX8

GO:0006351

transcription, DNA-templated

9590296

HgenePAX8

GO:0045893

positive regulation of transcription, DNA-templated

9388203|15356023|15961562

HgenePAX8

GO:0045944

positive regulation of transcription by RNA polymerase II

9388203

HgenePAX8

GO:0071371

cellular response to gonadotropin stimulus

15961562


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
TCGARVTHCATCGA-BJ-A291-01APAX8chr2

114035947

-GLIS1chr1

54065951

-
* 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-5UTRENST00000348715ENST00000312233PAX8chr2

114035947

-GLIS1chr1

54065951

-
5CDS-5UTRENST00000397647ENST00000312233PAX8chr2

114035947

-GLIS1chr1

54065951

-
5CDS-5UTRENST00000263335ENST00000312233PAX8chr2

114035947

-GLIS1chr1

54065951

-
5CDS-5UTRENST00000429538ENST00000312233PAX8chr2

114035947

-GLIS1chr1

54065951

-
5CDS-5UTRENST00000263334ENST00000312233PAX8chr2

114035947

-GLIS1chr1

54065951

-

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FusionProtFeatures for PAX8_GLIS1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PAX8

Q06710

GLIS1

Q8NBF1

Transcription factor for the thyroid-specific expressionof the genes exclusively expressed in the thyroid cell type,maintaining the functional differentiation of such cells. Acts as both a repressor and activator of transcription.Binds to the consensus sequence 5'-GACCACCCAC-3' (By similarity).{ECO:0000250|UniProtKB:Q8K1M4}.

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 PAX8_GLIS1


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 PAX8_GLIS1


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
PAX8NKX2-1, POU2AF1, CHUK, CXCL9, PKM, SERINC1, ANXA7, EP300, RB1GLIS1


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 PAX8_GLIS1


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 PAX8_GLIS1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePAX8C1869118HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS3CTD_human;ORPHANET;UNIPROT
HgenePAX8C0009404Colorectal Neoplasms1CTD_human
HgenePAX8C2931367Thyroid cancer, follicular1CTD_human