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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: 2149

FusionGeneSummary for APEH_APEH

check button Fusion gene summary
Fusion gene informationFusion gene name: APEH_APEH
Fusion gene ID: 2149
HgeneTgene
Gene symbol

APEH

APEH

Gene ID

327

327

Gene nameacylaminoacyl-peptide hydrolaseacylaminoacyl-peptide hydrolase
SynonymsAARE|ACPH|APH|D3F15S2|D3S48E|DNF15S2|OPHAARE|ACPH|APH|D3F15S2|D3S48E|DNF15S2|OPH
Cytomap

3p21.31

3p21.31

Type of geneprotein-codingprotein-coding
Descriptionacylamino-acid-releasing enzymeN-acylaminoacyl-peptide hydrolaseacyl-peptide hydrolaseacylaminoacyl-peptidaseoxidized protein hydrolaseacylamino-acid-releasing enzymeN-acylaminoacyl-peptide hydrolaseacyl-peptide hydrolaseacylaminoacyl-peptidaseoxidized protein hydrolase
Modification date2018051920180519
UniProtAcc

P13798

P13798

Ensembl transtripts involved in fusion geneENST00000296456, ENST00000438011, 
ENST00000296456, ENST00000438011, 
Fusion gene scores* DoF score2 X 2 X 1=42 X 2 X 1=4
# samples 22
** MAII scorelog2(2/4*10)=2.32192809488736log2(2/4*10)=2.32192809488736
Context

PubMed: APEH [Title/Abstract] AND APEH [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
HgeneAPEH

GO:0006508

proteolysis

17241160

HgeneAPEH

GO:0050435

amyloid-beta metabolic process

17241160

TgeneAPEH

GO:0006508

proteolysis

17241160

TgeneAPEH

GO:0050435

amyloid-beta metabolic process

17241160


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
ChiTaRS3.1AA639921APEHchr3

49720829

+APEHchr3

49720560

-
* 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
3UTR-3CDSENST00000296456ENST00000296456APEHchr3

49720829

+APEHchr3

49720560

-
3UTR-3CDSENST00000296456ENST00000438011APEHchr3

49720829

+APEHchr3

49720560

-
intron-3CDSENST00000438011ENST00000296456APEHchr3

49720829

+APEHchr3

49720560

-
intron-3CDSENST00000438011ENST00000438011APEHchr3

49720829

+APEHchr3

49720560

-

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FusionProtFeatures for APEH_APEH


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

P13798

APEH

P13798

This enzyme catalyzes the hydrolysis of the N-terminalpeptide bond of an N-acetylated peptide to generate an N-acetylated amino acid and a peptide with a free N-terminus. Itpreferentially cleaves off Ac-Ala, Ac-Met and Ac-Ser.{ECO:0000269|PubMed:1861871, ECO:0000269|PubMed:2006156}. This enzyme catalyzes the hydrolysis of the N-terminalpeptide bond of an N-acetylated peptide to generate an N-acetylated amino acid and a peptide with a free N-terminus. Itpreferentially cleaves off Ac-Ala, Ac-Met and Ac-Ser.{ECO:0000269|PubMed:1861871, ECO:0000269|PubMed:2006156}.

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 APEH_APEH


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 APEH_APEH


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 APEH_APEH


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 APEH_APEH


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