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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: 16478

FusionGeneSummary for HMGN2P46_ST14

check button Fusion gene summary
Fusion gene informationFusion gene name: HMGN2P46_ST14
Fusion gene ID: 16478
HgeneTgene
Gene symbol

HMGN2P46

ST14

Gene ID

283651

6768

Gene namehigh mobility group nucleosomal binding domain 2 pseudogene 46suppression of tumorigenicity 14
SynonymsC15orf21|D-PCa-2ARCI11|HAI|MT-SP1|MTSP1|PRSS14|SNC19|TADG15|TMPRSS14
Cytomap

15q21.1

11q24.3

Type of genepseudoprotein-coding
DescriptionDresden prostate cancer 2Dresden prostate carcinoma 2suppressor of tumorigenicity 14 proteinmembrane-type serine protease 1prostaminserine protease 14serine protease TADG-15suppression of tumorigenicity 14 (colon carcinoma)suppression of tumorigenicity 14 (colon carcinoma, matriptase, epithin)tumor a
Modification date2018051920180523
UniProtAcc

Q9Y5Y6

Ensembl transtripts involved in fusion geneENST00000409454, ENST00000278742, 
Fusion gene scores* DoF score6 X 4 X 1=244 X 3 X 3=36
# samples 54
** MAII scorelog2(5/24*10)=1.05889368905357
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/36*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: HMGN2P46 [Title/Abstract] AND ST14 [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
TgeneST14

GO:0006508

proteolysis

19911255


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
TCGALDPRADTCGA-H9-7775-01AHMGN2P46chr15

45806161

+ST14chr11

130058009

+
* 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-3CDSENST00000409454ENST00000278742HMGN2P46chr15

45806161

+ST14chr11

130058009

+

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FusionProtFeatures for HMGN2P46_ST14


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
HMGN2P46

ST14

Q9Y5Y6

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}. Degrades extracellular matrix. Proposed to play a rolein breast cancer invasion and metastasis. Exhibits trypsin-likeactivity as defined by cleavage of synthetic substrates with Argor Lys as the P1 site. Involved in the terminal differentiation ofkeratinocytes through prostasin (PRSS8) activation and filaggrin(FLG) processing. {ECO:0000269|PubMed:18843291}.

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 HMGN2P46_ST14


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 HMGN2P46_ST14


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
HMGN2P46ELAVL1ST14SPINT1, PDGFC, RGS16, AKT1, APC, CASP8, CDKN2C, CHEK2, NOTCH2, PHB, RAD51, STK11, TGFB1


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 HMGN2P46_ST14


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneST14Q9Y5Y6DB00013UrokinaseSuppressor of tumorigenicity 14 proteinbiotechapproved|investigational|withdrawn

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RelatedDiseases for HMGN2P46_ST14


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneST14C1835851Ichthyosis with hypotrichosis, autosomal recessive2CTD_human;ORPHANET;UNIPROT
TgeneST14C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneST14C0033578Prostatic Neoplasms1CTD_human
TgeneST14C0265962Ichthyosis linearis circumflexa1CTD_human