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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: 29502

FusionGeneSummary for PTPRF_ARTN

check button Fusion gene summary
Fusion gene informationFusion gene name: PTPRF_ARTN
Fusion gene ID: 29502
HgeneTgene
Gene symbol

PTPRF

ARTN

Gene ID

5792

9048

Gene nameprotein tyrosine phosphatase, receptor type Fartemin
SynonymsBNAH2|LARART|ENOVIN|EVN|NBN
Cytomap

1p34.2

1p34.1

Type of geneprotein-codingprotein-coding
Descriptionreceptor-type tyrosine-protein phosphatase FLCA-homologleukocyte antigen-related (LAR) PTP receptorleukocyte antigen-related tyrosine phosphataseleukocyte common antigen relatedprotein tyrosine phosphatase, receptor type, F polypeptidereceptor-linkearteminneublastin
Modification date2018052220180519
UniProtAcc

P10586

Q5T4W7

Ensembl transtripts involved in fusion geneENST00000359947, ENST00000438120, 
ENST00000372413, ENST00000372414, 
ENST00000422171, ENST00000496447, 
ENST00000414809, ENST00000372359, 
ENST00000498139, ENST00000479128, 
ENST00000472435, ENST00000372354, 
ENST00000438616, 
Fusion gene scores* DoF score10 X 9 X 7=6301 X 1 X 1=1
# samples 111
** MAII scorelog2(11/630*10)=-2.51784830486262
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: PTPRF [Title/Abstract] AND ARTN [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
TCGALDCOADTCGA-DM-A1D8-01APTPRFchr1

44058272

+ARTNchr1

44401327

+
* 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-5UTRENST00000359947ENST00000414809PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000359947ENST00000372359PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000359947ENST00000498139PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000359947ENST00000479128PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000359947ENST00000472435PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000359947ENST00000372354PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-intronENST00000359947ENST00000438616PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000438120ENST00000414809PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000438120ENST00000372359PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000438120ENST00000498139PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000438120ENST00000479128PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000438120ENST00000472435PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000438120ENST00000372354PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-intronENST00000438120ENST00000438616PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372413ENST00000414809PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372413ENST00000372359PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372413ENST00000498139PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372413ENST00000479128PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372413ENST00000472435PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372413ENST00000372354PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-intronENST00000372413ENST00000438616PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372414ENST00000414809PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372414ENST00000372359PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372414ENST00000498139PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372414ENST00000479128PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372414ENST00000472435PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000372414ENST00000372354PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-intronENST00000372414ENST00000438616PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000422171ENST00000414809PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000422171ENST00000372359PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000422171ENST00000498139PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000422171ENST00000479128PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000422171ENST00000472435PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-5UTRENST00000422171ENST00000372354PTPRFchr1

44058272

+ARTNchr1

44401327

+
5CDS-intronENST00000422171ENST00000438616PTPRFchr1

44058272

+ARTNchr1

44401327

+
intron-5UTRENST00000496447ENST00000414809PTPRFchr1

44058272

+ARTNchr1

44401327

+
intron-5UTRENST00000496447ENST00000372359PTPRFchr1

44058272

+ARTNchr1

44401327

+
intron-5UTRENST00000496447ENST00000498139PTPRFchr1

44058272

+ARTNchr1

44401327

+
intron-5UTRENST00000496447ENST00000479128PTPRFchr1

44058272

+ARTNchr1

44401327

+
intron-5UTRENST00000496447ENST00000472435PTPRFchr1

44058272

+ARTNchr1

44401327

+
intron-5UTRENST00000496447ENST00000372354PTPRFchr1

44058272

+ARTNchr1

44401327

+
intron-intronENST00000496447ENST00000438616PTPRFchr1

44058272

+ARTNchr1

44401327

+

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FusionProtFeatures for PTPRF_ARTN


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

P10586

ARTN

Q5T4W7

Possible cell adhesion receptor. It possesses anintrinsic protein tyrosine phosphatase activity (PTPase) anddephosphorylates EPHA2 regulating its activity. The first PTPase domain has enzymatic activity, whilethe second one seems to affect the substrate specificity of thefirst one. Ligand for the GFR-alpha-3-RET receptor complex but canalso activate the GFR-alpha-1-RET receptor complex. Supports thesurvival of sensory and sympathetic peripheral neurons in cultureand also supports the survival of dopaminergic neurons of theventral mid-brain. Strong attractant of gut hematopoietic cellsthus promoting the formation Peyer's patch-like structures, amajor component of the gut-associated lymphoid tissue.{ECO:0000269|PubMed:10583383, ECO:0000269|PubMed:9883723}.

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 PTPRF_ARTN


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 PTPRF_ARTN


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
PTPRFCTNNB1, GIT1, PPFIA1, RET, TRIO, CAV1, NID1, JUP, PPFIA3, PPFIA2, RYK, PRPF40A, SKIL, ZNF512B, EGFR, CUL7, ABCE1, CEACAM21, TGFBR2, SCN2B, HEPACAM2, UNK, NTRK1, ADRBK1, DNAAF5, NAA50, NPLOC4, PFKM, PICALM, PPWD1, ARPC3, HACL1, MAPK1, PPP2R5D, SEPHS1, TSTA3, UFD1L, CDKN2AIP, NUDCD3, TTI1, FAM171A2, SUGT1, PTPRS, WFDC2, IL13RA2, CLU, LRRIQ1, TMEM30B, PCDHGB1, ATP6V0E1, MANSC1, PCDHB16, MRAP2, PIANP, TRIM25ARTNGFRA3


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 PTPRF_ARTN


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 PTPRF_ARTN


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePTPRFC0038356Stomach Neoplasms1CTD_human
HgenePTPRFC0345967Malignant mesothelioma1CTD_human
TgeneARTNC0011570Mental Depression5PSYGENET
TgeneARTNC0011581Depressive disorder5PSYGENET
TgeneARTNC0041696Unipolar Depression4PSYGENET
TgeneARTNC1269683Major Depressive Disorder4PSYGENET
TgeneARTNC0005586Bipolar Disorder1PSYGENET
TgeneARTNC1458155Mammary Neoplasms1CTD_human