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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: 2044

FusionGeneSummary for AP1S2_AP1S2

check button Fusion gene summary
Fusion gene informationFusion gene name: AP1S2_AP1S2
Fusion gene ID: 2044
HgeneTgene
Gene symbol

AP1S2

AP1S2

Gene ID

8905

8905

Gene nameadaptor related protein complex 1 subunit sigma 2adaptor related protein complex 1 subunit sigma 2
SynonymsDC22|MRX59|MRXS21|MRXS5|MRXSF|PGS|SIGMA1BDC22|MRX59|MRXS21|MRXS5|MRXSF|PGS|SIGMA1B
Cytomap

Xp22.2

Xp22.2

Type of geneprotein-codingprotein-coding
DescriptionAP-1 complex subunit sigma-2adapter-related protein complex 1 sigma-1B subunitadaptor protein complex AP-1 sigma-1B subunitadaptor related protein complex 1 sigma 2 subunitadaptor-related protein complex 1 subunit sigma-1Bclathrin adaptor complex AP1AP-1 complex subunit sigma-2adapter-related protein complex 1 sigma-1B subunitadaptor protein complex AP-1 sigma-1B subunitadaptor related protein complex 1 sigma 2 subunitadaptor-related protein complex 1 subunit sigma-1Bclathrin adaptor complex AP1
Modification date2018051920180519
UniProtAcc

P56377

P56377

Ensembl transtripts involved in fusion geneENST00000329235, ENST00000380291, 
ENST00000479184, ENST00000545766, 
ENST00000421527, 
ENST00000329235, 
ENST00000380291, ENST00000479184, 
ENST00000545766, ENST00000421527, 
Fusion gene scores* DoF score2 X 2 X 1=42 X 2 X 2=8
# samples 22
** MAII scorelog2(2/4*10)=2.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: AP1S2 [Title/Abstract] AND AP1S2 [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

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
ChiTaRS3.1AA193118AP1S2chrX

15844416

+AP1S2chrX

15844518

-
* 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-3UTRENST00000329235ENST00000329235AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000329235ENST00000380291AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000329235ENST00000479184AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000329235ENST00000545766AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000329235ENST00000421527AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-3UTRENST00000380291ENST00000329235AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000380291ENST00000380291AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000380291ENST00000479184AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000380291ENST00000545766AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000380291ENST00000421527AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-3UTRENST00000479184ENST00000329235AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000479184ENST00000380291AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000479184ENST00000479184AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000479184ENST00000545766AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000479184ENST00000421527AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-3UTRENST00000545766ENST00000329235AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000545766ENST00000380291AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000545766ENST00000479184AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000545766ENST00000545766AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000545766ENST00000421527AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-3UTRENST00000421527ENST00000329235AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000421527ENST00000380291AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000421527ENST00000479184AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000421527ENST00000545766AP1S2chrX

15844416

+AP1S2chrX

15844518

-
intron-intronENST00000421527ENST00000421527AP1S2chrX

15844416

+AP1S2chrX

15844518

-

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FusionProtFeatures for AP1S2_AP1S2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
AP1S2

P56377

AP1S2

P56377

Subunit of clathrin-associated adaptor protein complex 1that plays a role in protein sorting in the late-Golgi/trans-Golginetwork (TGN) and/or endosomes. The AP complexes mediate both therecruitment of clathrin to membranes and the recognition ofsorting signals within the cytosolic tails of transmembrane cargomolecules. Subunit of clathrin-associated adaptor protein complex 1that plays a role in protein sorting in the late-Golgi/trans-Golginetwork (TGN) and/or endosomes. The AP complexes mediate both therecruitment of clathrin to membranes and the recognition ofsorting signals within the cytosolic tails of transmembrane cargomolecules.

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 AP1S2_AP1S2


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 AP1S2_AP1S2


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 AP1S2_AP1S2


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 AP1S2_AP1S2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneAP1S2C0796254DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES3CTD_human;ORPHANET
HgeneAP1S2C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneAP1S2C0796254DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES3CTD_human;ORPHANET
TgeneAP1S2C0023893Liver Cirrhosis, Experimental1CTD_human