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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: 36216

FusionGeneSummary for ST14_APLP2

check button Fusion gene summary
Fusion gene informationFusion gene name: ST14_APLP2
Fusion gene ID: 36216
HgeneTgene
Gene symbol

ST14

APLP2

Gene ID

6768

334

Gene namesuppression of tumorigenicity 14amyloid beta precursor like protein 2
SynonymsARCI11|HAI|MT-SP1|MTSP1|PRSS14|SNC19|TADG15|TMPRSS14APLP-2|APPH|APPL2|CDEBP
Cytomap

11q24.3

11q24.3

Type of geneprotein-codingprotein-coding
Descriptionsuppressor 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 aamyloid-like protein 2CDEI box-binding proteinamyloid beta (A4) precursor-like protein 2amyloid precursor protein homolog HSD-2testicular tissue protein Li 23
Modification date2018052320180519
UniProtAcc

Q9Y5Y6

Q06481

Ensembl transtripts involved in fusion geneENST00000278742, ENST00000532456, 
ENST00000539648, ENST00000528499, 
ENST00000263574, ENST00000345598, 
ENST00000338167, ENST00000278756, 
ENST00000543137, 
Fusion gene scores* DoF score6 X 5 X 5=1505 X 8 X 3=120
# samples 78
** MAII scorelog2(7/150*10)=-1.09953567355091
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/120*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ST14 [Title/Abstract] AND APLP2 [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
HgeneST14

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
TCGARVPRADTCGA-HC-8265-01AST14chr11

130029955

+APLP2chr11

129979324

+
TCGARVUCECTCGA-B5-A3S1-01AST14chr11

130078579

+APLP2chr11

130010293

+
* 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
5CDS-3UTRENST00000278742ENST00000532456ST14chr11

130029955

+APLP2chr11

129979324

+
5CDS-intronENST00000278742ENST00000539648ST14chr11

130029955

+APLP2chr11

129979324

+
5CDS-intronENST00000278742ENST00000528499ST14chr11

130029955

+APLP2chr11

129979324

+
5CDS-intronENST00000278742ENST00000263574ST14chr11

130029955

+APLP2chr11

129979324

+
5CDS-intronENST00000278742ENST00000345598ST14chr11

130029955

+APLP2chr11

129979324

+
5CDS-intronENST00000278742ENST00000338167ST14chr11

130029955

+APLP2chr11

129979324

+
5CDS-intronENST00000278742ENST00000278756ST14chr11

130029955

+APLP2chr11

129979324

+
5CDS-5UTRENST00000278742ENST00000543137ST14chr11

130029955

+APLP2chr11

129979324

+
5CDS-intronENST00000278742ENST00000532456ST14chr11

130078579

+APLP2chr11

130010293

+
5CDS-intronENST00000278742ENST00000539648ST14chr11

130078579

+APLP2chr11

130010293

+
5CDS-intronENST00000278742ENST00000528499ST14chr11

130078579

+APLP2chr11

130010293

+
5CDS-intronENST00000278742ENST00000263574ST14chr11

130078579

+APLP2chr11

130010293

+
5CDS-intronENST00000278742ENST00000345598ST14chr11

130078579

+APLP2chr11

130010293

+
5CDS-intronENST00000278742ENST00000338167ST14chr11

130078579

+APLP2chr11

130010293

+
5CDS-intronENST00000278742ENST00000278756ST14chr11

130078579

+APLP2chr11

130010293

+
5CDS-intronENST00000278742ENST00000543137ST14chr11

130078579

+APLP2chr11

130010293

+

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FusionProtFeatures for ST14_APLP2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ST14

Q9Y5Y6

APLP2

Q06481

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 ST14_APLP2


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 ST14_APLP2


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
ST14SPINT1, PDGFC, RGS16, AKT1, APC, CASP8, CDKN2C, CHEK2, NOTCH2, PHB, RAD51, STK11, TGFB1APLP2BRCA1, SFN, DAB2, DAB1, APBB1, APBB3, HGS, JUN, RYK, HDAC5, KAT5, ELAVL1, BAG6, VKORC1, ZNF512B, MAPK8, RPL26, DEDD, ETS1, JUNB, KLK2, APBB2, PTPN1, PTPN2, VAV1, APBA3, FCGRT, DKKL1, NKTR, TRIM25


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 ST14_APLP2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneST14Q9Y5Y6DB00013UrokinaseSuppressor of tumorigenicity 14 proteinbiotechapproved|investigational|withdrawn
TgeneAPLP2Q06481DB01593ZincAmyloid-like protein 2small moleculeapproved|investigational

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RelatedDiseases for ST14_APLP2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneST14C1835851Ichthyosis with hypotrichosis, autosomal recessive2CTD_human;ORPHANET;UNIPROT
HgeneST14C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneST14C0033578Prostatic Neoplasms1CTD_human
HgeneST14C0265962Ichthyosis linearis circumflexa1CTD_human
TgeneAPLP2C0027746Nerve Degeneration1CTD_human
TgeneAPLP2C0151744Myocardial Ischemia1CTD_human