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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: 29057

FusionGeneSummary for PSAP_PTN

check button Fusion gene summary
Fusion gene informationFusion gene name: PSAP_PTN
Fusion gene ID: 29057
HgeneTgene
Gene symbol

PSAP

PTN

Gene ID

729238

5764

Gene namesurfactant protein A2pleiotrophin
SynonymsCOLEC5|PSAP|PSP-A|PSPA|SFTP1|SFTPA2B|SP-2A|SP-A|SPA2|SPAIIHARP|HB-GAM|HBBM|HBGF-8|HBGF8|HBNF|HBNF-1|NEGF1|OSF-1
Cytomap

10q22.3

7q33

Type of geneprotein-codingprotein-coding
Descriptionpulmonary surfactant-associated protein A235 kDa pulmonary surfactant-associated proteinalveolar proteinosis proteincollectin 5surfactant, pulmonary-associated protein A2Apleiotrophinheparin affin regulatory proteinheparin-binding brain mitogenheparin-binding growth factor 8heparin-binding growth-associated moleculeheparin-binding neurite outgrowth promoting factorheparin-binding neurite outgrowth-promoting factor 1
Modification date2018052320180523
UniProtAcc

P07602

P21246

Ensembl transtripts involved in fusion geneENST00000394936, ENST00000394934, 
ENST00000348225, ENST00000393083, 
Fusion gene scores* DoF score32 X 20 X 10=64006 X 2 X 5=60
# samples 376
** MAII scorelog2(37/6400*10)=-4.11247472925841
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/60*10)=0
Context

PubMed: PSAP [Title/Abstract] AND PTN [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
TgenePTN

GO:0008284

positive regulation of cell proliferation

1733956


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
TCGARVUCECTCGA-AX-A3G6-01APSAPchr10

73576056

-PTNchr7

136938384

-
* 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
Frame-shiftENST00000394936ENST00000348225PSAPchr10

73576056

-PTNchr7

136938384

-
Frame-shiftENST00000394936ENST00000393083PSAPchr10

73576056

-PTNchr7

136938384

-
Frame-shiftENST00000394934ENST00000348225PSAPchr10

73576056

-PTNchr7

136938384

-
Frame-shiftENST00000394934ENST00000393083PSAPchr10

73576056

-PTNchr7

136938384

-

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FusionProtFeatures for PSAP_PTN


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

P07602

PTN

P21246

Secreted growth factor that induces neurite outgrowthand which is mitogenic for fibroblasts, epithelial, andendothelial cells (PubMed:1768439, PubMed:1733956). Bindsanaplastic lymphoma kinase (ALK) which induces MAPK pathwayactivation, an important step in the anti-apoptotic signaling ofPTN and regulation of cell proliferation (PubMed:11278720). Bindsto cell-surface target proteins via their chondroitin sulfategroups (PubMed:26896299). Down-regulates PTPRZ1 activity(PubMed:16814777). {ECO:0000269|PubMed:11278720,ECO:0000269|PubMed:16814777, ECO:0000269|PubMed:1768439,ECO:0000269|PubMed:26896299}.

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 PSAP_PTN


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 PSAP_PTN


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
PSAPCELSR1, SGK223, MAFF, COPS6, CTSD, PSAP, UBE3A, ZBED1, USP4, TCERG1, SMARCC2, SAP18, PLAUR, SNAP23, NUP133, DNAJA1, SURF4, GDAP1, U2AF1, SNRPA1, SUMO2, SNCA, SRSF5, SSR1, THRAP3, BRCA1, SMAD9, SMAD2, CFTR, FBXO6, BAG3, BCAT1, C1QBP, GTF2F1, LAMB2, MVP, USP48, VPS29, VPS35, ERBB2, NLGN3, SOD1PTNAPOBEC3G, CGA, DFNA5, HSPBAP1, TAF1D, MKKS, PLXNB2, SUPT7L, WFDC2, ATRX, BMI1, BTBD2, CAAP1, CACNB4, CDH10, CDK5RAP2, COX6C, DUSP12, EVA1A, FTL, BLOC1S1, GLYAT, GTF2F1, ITSN2, MLLT3, MYCBP, NAP1L5, CRCT1, PMF1, PSMB10, RIT1, RBM23, SNCAIP, STC2, TAC3, TBRG4, TXNDC9, ARL15, ATP5C1, CAPZB, CCDC53, CRELD1, DNAJB11, EIF3F, SLC25A36, GPD1, GSTP1, LAMA4, LUC7L2, MAD2L1BP, P4HB, UTP3, SAT1, SSR1, TP53BP2, ARIH2, GIPC2, GNB2L1, HGH1, PPP2CA, PSMD11, PTPRS, RPLP1, SGSM2, TOMM20, UBQLN4, PSMD2, CHD3, SGTA, BCCIP, ALK, PTPRZ1, CTNNB1, NUDT21, GSK3B, MRPL44, C7orf25, BCL2L1, PFDN1, GADD45A, C11orf58, BARD1, KPNB1, GADD45G, FEZ1, PTN, PIAS4, GPRASP2, BAG6, TSC22D1, CYP2E1, UBQLN1, NEK6, PTPRB


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 PSAP_PTN


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 PSAP_PTN


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePSAPC0268262Metachromatic Leukodystrophy due to Saposin B Deficiency5CTD_human;UNIPROT
HgenePSAPC1864651GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY2CTD_human;ORPHANET;UNIPROT
TgenePTNC0023893Liver Cirrhosis, Experimental1CTD_human
TgenePTNC0024667Animal Mammary Neoplasms1CTD_human
TgenePTNC0024668Mammary Neoplasms, Experimental1CTD_human