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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: 36206

FusionGeneSummary for SST_ANKRD52

check button Fusion gene summary
Fusion gene informationFusion gene name: SST_ANKRD52
Fusion gene ID: 36206
HgeneTgene
Gene symbol

SST

ANKRD52

Gene ID

6750

283373

Gene namesomatostatinankyrin repeat domain 52
SynonymsSMSTANKRD33
Cytomap

3q27.3

12q13.3

Type of geneprotein-codingprotein-coding
Descriptionsomatostatingrowth hormone release-inhibiting factorprepro-somatostatinsomatostatin-14somatostatin-28serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit CCVWG5837PP6-ARS-Cankyrin repeat domain 33ankyrin repeat domain-containing protein 52protein phosphatase 6 ankyrin repeat subunit Cserine/threonine-protein phosphatase 6 regula
Modification date2018052320180519
UniProtAcc

P61278

Q8NB46

Ensembl transtripts involved in fusion geneENST00000287641, ENST00000548241, 
ENST00000267116, 
Fusion gene scores* DoF score2 X 2 X 1=43 X 3 X 3=27
# samples 23
** MAII scorelog2(2/4*10)=2.32192809488736log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SST [Title/Abstract] AND ANKRD52 [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
ChiTaRS3.1DB303581SSTchr3

187386808

+ANKRD52chr12

56636333

+
* 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-intronENST00000287641ENST00000548241SSTchr3

187386808

+ANKRD52chr12

56636333

+
intron-3UTRENST00000287641ENST00000267116SSTchr3

187386808

+ANKRD52chr12

56636333

+

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FusionProtFeatures for SST_ANKRD52


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

P61278

ANKRD52

Q8NB46

Somatostatin inhibits the release of somatotropin. Putative regulatory subunit of protein phosphatase 6(PP6) that may be involved in the recognition of phosphoproteinsubstrates.

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 SST_ANKRD52


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 SST_ANKRD52


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 SST_ANKRD52


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneSSTP61278DB00847CysteamineSomatostatinsmall moleculeapproved|investigational

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RelatedDiseases for SST_ANKRD52


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSSTC0036341Schizophrenia5PSYGENET
HgeneSSTC0036572Seizures3CTD_human
HgeneSSTC0041696Unipolar Depression2PSYGENET
HgeneSSTC1269683Major Depressive Disorder2PSYGENET
HgeneSSTC0000786Spontaneous abortion1CTD_human
HgeneSSTC0004763Barrett Esophagus1CTD_human
HgeneSSTC0005586Bipolar Disorder1PSYGENET
HgeneSSTC0011993Vipoma1CTD_human
HgeneSSTC0014175Endometriosis1CTD_human
HgeneSSTC0014849Esophageal and Gastric Varices1CTD_human
HgeneSSTC0014859Esophageal Neoplasms1CTD_human
HgeneSSTC0020621Hypokalemia1CTD_human
HgeneSSTC0022116Ischemia1CTD_human
HgeneSSTC0026766Multiple Organ Failure1CTD_human
HgeneSSTC0030297Pancreatic Neoplasm1CTD_human
HgeneSSTC0030305Pancreatitis1CTD_human
HgeneSSTC0036337Schizoaffective Disorder1PSYGENET
HgeneSSTC0525045Mood Disorders1CTD_human