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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: 462

FusionGeneSummary for ACPP_OGT

check button Fusion gene summary
Fusion gene informationFusion gene name: ACPP_OGT
Fusion gene ID: 462
HgeneTgene
Gene symbol

ACPP

OGT

Gene ID

55

8473

Gene nameacid phosphatase, prostateO-linked N-acetylglucosamine (GlcNAc) transferase
Synonyms5'-NT|ACP-3|ACP3HINCUT-1|HRNT1|MRX106|O-GLCNAC|OGT1
Cytomap

3q22.1

Xq13.1

Type of geneprotein-codingprotein-coding
Descriptionprostatic acid phosphataseTMPaseecto-5'-nucleotidaseprostatic acid phosphotasethiamine monophosphataseUDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunitO-GlcNAc transferase p110 subunitO-GlcNAc transferase subunit p110O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminy
Modification date2018051920180519
UniProtAcc

P15309

O15294

Ensembl transtripts involved in fusion geneENST00000336375, ENST00000475741, 
ENST00000351273, ENST00000489084, 
ENST00000373719, ENST00000373701, 
ENST00000498566, 
Fusion gene scores* DoF score13 X 6 X 2=1562 X 1 X 1=2
# samples 152
** MAII scorelog2(15/156*10)=-0.0565835283663674
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/2*10)=3.32192809488736
Context

PubMed: ACPP [Title/Abstract] AND OGT [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
HgeneACPP

GO:0046085

adenosine metabolic process

18940592

HgeneACPP

GO:0051289

protein homotetramerization

10639192

TgeneOGT

GO:0006110

regulation of glycolytic process

22923583

TgeneOGT

GO:0006493

protein O-linked glycosylation

21240259|21285374|22923583|23222540|23352454|24474760

TgeneOGT

GO:0006915

apoptotic process

20824293

TgeneOGT

GO:0032868

response to insulin

18288188

TgeneOGT

GO:0035020

regulation of Rac protein signal transduction

18288188

TgeneOGT

GO:0043981

histone H4-K5 acetylation

20018852

TgeneOGT

GO:0043982

histone H4-K8 acetylation

20018852

TgeneOGT

GO:0043984

histone H4-K16 acetylation

20018852

TgeneOGT

GO:0045862

positive regulation of proteolysis

21285374

TgeneOGT

GO:0045944

positive regulation of transcription by RNA polymerase II

23222540|23353889

TgeneOGT

GO:0046626

regulation of insulin receptor signaling pathway

18288188

TgeneOGT

GO:0048015

phosphatidylinositol-mediated signaling

18288188


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
TCGARVPRADTCGA-EJ-5512-01AACPPchr3

132077596

+OGTchrX

70782980

+
* 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
Frame-shiftENST00000336375ENST00000373719ACPPchr3

132077596

+OGTchrX

70782980

+
Frame-shiftENST00000336375ENST00000373701ACPPchr3

132077596

+OGTchrX

70782980

+
5CDS-intronENST00000336375ENST00000498566ACPPchr3

132077596

+OGTchrX

70782980

+
intron-3CDSENST00000475741ENST00000373719ACPPchr3

132077596

+OGTchrX

70782980

+
intron-3CDSENST00000475741ENST00000373701ACPPchr3

132077596

+OGTchrX

70782980

+
intron-intronENST00000475741ENST00000498566ACPPchr3

132077596

+OGTchrX

70782980

+
intron-3CDSENST00000351273ENST00000373719ACPPchr3

132077596

+OGTchrX

70782980

+
intron-3CDSENST00000351273ENST00000373701ACPPchr3

132077596

+OGTchrX

70782980

+
intron-intronENST00000351273ENST00000498566ACPPchr3

132077596

+OGTchrX

70782980

+
intron-3CDSENST00000489084ENST00000373719ACPPchr3

132077596

+OGTchrX

70782980

+
intron-3CDSENST00000489084ENST00000373701ACPPchr3

132077596

+OGTchrX

70782980

+
intron-intronENST00000489084ENST00000498566ACPPchr3

132077596

+OGTchrX

70782980

+

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FusionProtFeatures for ACPP_OGT


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

P15309

OGT

O15294

A non-specific tyrosine phosphatase thatdephosphorylates a diverse number of substrates under acidicconditions (pH 4-6) including alkyl, aryl, and acyl orthophosphatemonoesters and phosphorylated proteins. Has lipid phosphataseactivity and inactivates lysophosphatidic acid in seminal plasma. Isoform 2: the cellular form also has ecto-5'-nucleotidase activity in dorsal root ganglion (DRG) neurons.Generates adenosine from AMP which acts as a pain suppressor. Actsas a tumor suppressor of prostate cancer through dephosphorylationof ERBB2 and deactivation of MAPK-mediated signaling. Catalyzes the transfer of a single N-acetylglucosaminefrom UDP-GlcNAc to a serine or threonine residue in cytoplasmicand nuclear proteins resulting in their modification with a beta-linked N-acetylglucosamine (O-GlcNAc) (PubMed:26678539).Glycosylates a large and diverse number of proteins includinghistone H2B, AKT1, EZH2, PFKL, KMT2E/MLL5, MAPT/TAU and HCFC1(PubMed:26678539). Can regulate their cellular processes viacross-talk between glycosylation and phosphorylation or byaffecting proteolytic processing (PubMed:26678539). Probably byglycosylating KMT2E/MLL5, stabilizes KMT2E/MLL5 by preventing itsubiquitination (PubMed:26678539). Involved in insulin resistancein muscle and adipocyte cells via glycosylating insulin signalingcomponents and inhibiting the 'Thr-308' phosphorylation of AKT1,enhancing IRS1 phosphorylation and attenuating insulin signaling.Involved in glycolysis regulation by mediating glycosylation of 6-phosphofructokinase PFKL, inhibiting its activity(PubMed:22923583). Component of a THAP1/THAP3-HCFC1-OGT complexthat is required for the regulation of the transcriptionalactivity of RRM1. Plays a key role in chromatin structure bymediating O-GlcNAcylation of 'Ser-112' of histone H2B: recruitedto CpG-rich transcription start sites of active genes via itsinteraction with TET proteins (TET1, TET2 or TET3)(PubMed:22121020, PubMed:23353889). As part of the NSL complexindirectly involved in acetylation of nucleosomal histone H4 onseveral lysine residues (PubMed:20018852). O-GlcNAcylation of'Ser-75' of EZH2 increases its stability, and facilitating theformation of H3K27me3 by the PRC2/EED-EZH2 complex(PubMed:24474760). Regulates circadian oscillation of the clockgenes and glucose homeostasis in the liver. Stabilizes clockproteins ARNTL/BMAL1 and CLOCK through O-glycosylation, whichprevents their ubiquitination and subsequent degradation. Promotesthe CLOCK-ARNTL/BMAL1-mediated transcription of genes in thenegative loop of the circadian clock such as PER1/2 and CRY1/2(PubMed:12150998, PubMed:18288188, PubMed:19377461,PubMed:19451179, PubMed:20018868, PubMed:20200153,PubMed:21285374, PubMed:15361863). O-glycosylates HCFC1 andregulates its proteolytic processing and transcriptional activity(PubMed:21285374, PubMed:28584052, PubMed:28302723).{ECO:0000269|PubMed:12150998, ECO:0000269|PubMed:15361863,ECO:0000269|PubMed:18288188, ECO:0000269|PubMed:19451179,ECO:0000269|PubMed:20018852, ECO:0000269|PubMed:20018868,ECO:0000269|PubMed:20200153, ECO:0000269|PubMed:21285374,ECO:0000269|PubMed:22121020, ECO:0000269|PubMed:22923583,ECO:0000269|PubMed:23353889, ECO:0000269|PubMed:24474760,ECO:0000269|PubMed:26678539, ECO:0000269|PubMed:28302723,ECO:0000269|PubMed:28584052}. Isoform 2: the mitochondrial isoform (mOGT) is cytotoxicand triggers apoptosis in several cell types including INS1, aninsulinoma cell line.

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 ACPP_OGT


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 ACPP_OGT


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
ACPPACPP, UBC, SHBG, MMRN1, DDX19B, RPS6KB2, TBC1D22B, FTH1, CDK15, CCDC103, CPLX3, FBXL4, AIRE, ZIC1, DUSP21, IL31RA, FCRL5, KIF3A, NPPA, HSF2, FCF1, LACC1, L2HGDHOGTNUP62CL, FIBP, CDK2, WRAP73, TRAK1, HCFC1, SIN3A, BAP1, BTRC, FBXW11, THAP3, THAP1, MGEA5, SAP25, NUP62, CSNK2A1, MAPT, YES1, KAT8, HDAC5, TAB1, PPP1CA, PPP1CB, RELA, NFATC1, SMURF1, FOXO4, UBL4A, ACTR2, AGFG1, ALAD, C14orf142, DBNL, GPN1, HSPBP1, LAP3, P3H1, LPP, PPME1, RPRD1B, SURF2, TOM1L1, WDR4, ZPR1, WWOX, HUWE1, PSG1, TET2, PHC3, NXF1, TRAK2, DDAH2, CREB3, THAP11, KCMF1, UNK, CRKL, FARSA, FARSB, GIPC1, PDXK, PSPH, TPD52L2, PAFAH1B2, NTRK1, CSNK2B, DYNLT1, AK1, KIF5B, RTFDC1, RBPJ, TCF4, ASXL1, ASXL2, KMT2E, USP7, KLF5, RC3H1, PHF8, KDM1B, CIART, HCFC1R1, HCFC2, THAP2, CAMK2D, UBC, UNC119, NPHP3, CYLD, TRIM25, BRCA1


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 ACPP_OGT


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneACPPP15309DB06688Sipuleucel-TProstatic acid phosphatasebiotechapproved|investigational

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RelatedDiseases for ACPP_OGT


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneACPPC3495559Juvenile arthritis1CTD_human