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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: 14986

FusionGeneSummary for GNPAT_GNPAT

check button Fusion gene summary
Fusion gene informationFusion gene name: GNPAT_GNPAT
Fusion gene ID: 14986
HgeneTgene
Gene symbol

GNPAT

GNPAT

Gene ID

8443

8443

Gene nameglyceronephosphate O-acyltransferaseglyceronephosphate O-acyltransferase
SynonymsDAP-AT|DAPAT|DHAPAT|RCDP2DAP-AT|DAPAT|DHAPAT|RCDP2
Cytomap

1q42.2

1q42.2

Type of geneprotein-codingprotein-coding
Descriptiondihydroxyacetone phosphate acyltransferaseDHAP-ATacyl-CoA:dihydroxyacetonephosphateacyltransferaseglycerone-phosphate O-acyltransferasedihydroxyacetone phosphate acyltransferaseDHAP-ATacyl-CoA:dihydroxyacetonephosphateacyltransferaseglycerone-phosphate O-acyltransferase
Modification date2018052320180523
UniProtAcc

O15228

O15228

Ensembl transtripts involved in fusion geneENST00000366647, ENST00000366646, 
ENST00000469332, 
ENST00000366647, 
ENST00000366646, ENST00000469332, 
Fusion gene scores* DoF score4 X 4 X 4=644 X 4 X 2=32
# samples 54
** MAII scorelog2(5/64*10)=-0.356143810225275
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: GNPAT [Title/Abstract] AND GNPAT [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
HgeneGNPAT

GO:0008611

ether lipid biosynthetic process

15687349

TgeneGNPAT

GO:0008611

ether lipid biosynthetic process

15687349


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
ChiTaRS3.1AW810786GNPATchr1

231393186

-GNPATchr1

231392635

+
* 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-intronENST00000366647ENST00000366647GNPATchr1

231393186

-GNPATchr1

231392635

+
intron-intronENST00000366647ENST00000366646GNPATchr1

231393186

-GNPATchr1

231392635

+
intron-intronENST00000366647ENST00000469332GNPATchr1

231393186

-GNPATchr1

231392635

+
intron-intronENST00000366646ENST00000366647GNPATchr1

231393186

-GNPATchr1

231392635

+
intron-intronENST00000366646ENST00000366646GNPATchr1

231393186

-GNPATchr1

231392635

+
intron-intronENST00000366646ENST00000469332GNPATchr1

231393186

-GNPATchr1

231392635

+
intron-intronENST00000469332ENST00000366647GNPATchr1

231393186

-GNPATchr1

231392635

+
intron-intronENST00000469332ENST00000366646GNPATchr1

231393186

-GNPATchr1

231392635

+
intron-intronENST00000469332ENST00000469332GNPATchr1

231393186

-GNPATchr1

231392635

+

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FusionProtFeatures for GNPAT_GNPAT


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

O15228

GNPAT

O15228


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 GNPAT_GNPAT


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 GNPAT_GNPAT


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 GNPAT_GNPAT


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 GNPAT_GNPAT


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGNPATC1857242Rhizomelic chondrodysplasia punctata, type 22CTD_human;ORPHANET;UNIPROT
HgeneGNPATC0036341Schizophrenia1PSYGENET
TgeneGNPATC1857242Rhizomelic chondrodysplasia punctata, type 22CTD_human;ORPHANET;UNIPROT
TgeneGNPATC0036341Schizophrenia1PSYGENET