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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: 14995

FusionGeneSummary for GNPNAT1_STYX

check button Fusion gene summary
Fusion gene informationFusion gene name: GNPNAT1_STYX
Fusion gene ID: 14995
HgeneTgene
Gene symbol

GNPNAT1

STYX

Gene ID

64841

6815

Gene nameglucosamine-phosphate N-acetyltransferase 1serine/threonine/tyrosine interacting protein
SynonymsGNA1|GNPNAT|Gpnat1-
Cytomap

14q22.1

14q22.1

Type of geneprotein-codingprotein-coding
Descriptionglucosamine 6-phosphate N-acetyltransferasephosphoglucosamine acetylasephosphoglucosamine transacetylaseserine/threonine/tyrosine-interacting proteinprotein tyrosine phosphatase-like protein
Modification date2018052320180523
UniProtAcc

Q96EK6

Q8WUJ0

Ensembl transtripts involved in fusion geneENST00000216410, ENST00000554421, 
ENST00000554230, 
ENST00000442123, 
ENST00000354586, ENST00000556861, 
Fusion gene scores* DoF score2 X 2 X 1=45 X 5 X 2=50
# samples 25
** MAII scorelog2(2/4*10)=2.32192809488736log2(5/50*10)=0
Context

PubMed: GNPNAT1 [Title/Abstract] AND STYX [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
TgeneSTYX

GO:0032091

negative regulation of protein binding

28007894


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
ChiTaRS3.1DW412766GNPNAT1chr14

53255709

+STYXchr14

53241434

+
* 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-3UTRENST00000216410ENST00000442123GNPNAT1chr14

53255709

+STYXchr14

53241434

+
intron-3UTRENST00000216410ENST00000354586GNPNAT1chr14

53255709

+STYXchr14

53241434

+
intron-intronENST00000216410ENST00000556861GNPNAT1chr14

53255709

+STYXchr14

53241434

+
intron-3UTRENST00000554421ENST00000442123GNPNAT1chr14

53255709

+STYXchr14

53241434

+
intron-3UTRENST00000554421ENST00000354586GNPNAT1chr14

53255709

+STYXchr14

53241434

+
intron-intronENST00000554421ENST00000556861GNPNAT1chr14

53255709

+STYXchr14

53241434

+
intron-3UTRENST00000554230ENST00000442123GNPNAT1chr14

53255709

+STYXchr14

53241434

+
intron-3UTRENST00000554230ENST00000354586GNPNAT1chr14

53255709

+STYXchr14

53241434

+
intron-intronENST00000554230ENST00000556861GNPNAT1chr14

53255709

+STYXchr14

53241434

+

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FusionProtFeatures for GNPNAT1_STYX


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GNPNAT1

Q96EK6

STYX

Q8WUJ0

Catalytically inactive phosphatase (PubMed:23847209).Acts as a nuclear anchor for MAPK1/MAPK3 (ERK1/ERK2)(PubMed:23847209). Modulates cell-fate decisions and cellmigration by spatiotemporal regulation of MAPK1/MAPK3 (ERK1/ERK2)(PubMed:23847209). By binding to the F-box of FBXW7, prevents theassembly of FBXW7 into the SCF E3 ubiquitin-protein ligasecomplex, and thereby inhibits degradation of its substrates(PubMed:28007894). Plays a role in spermatogenesis (Bysimilarity). {ECO:0000250|UniProtKB:Q60969,ECO:0000269|PubMed:23847209, ECO:0000269|PubMed:28007894}.

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 GNPNAT1_STYX


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 GNPNAT1_STYX


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 GNPNAT1_STYX


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 GNPNAT1_STYX


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