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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: 27343

FusionGeneSummary for PITX1_SH3BGRL3

check button Fusion gene summary
Fusion gene informationFusion gene name: PITX1_SH3BGRL3
Fusion gene ID: 27343
HgeneTgene
Gene symbol

PITX1

SH3BGRL3

Gene ID

5307

83442

Gene namepaired like homeodomain 1SH3 domain binding glutamate rich protein like 3
SynonymsBFT|CCF|LBNBG|POTX|PTX1HEL-S-297|SH3BP-1|TIP-B1
Cytomap

5q31.1

1p36.11

Type of geneprotein-codingprotein-coding
Descriptionpituitary homeobox 1hindlimb expressed homeobox protein backfoothomeobox protein PITX1paired-like homeodomain transcription factor 1pituitary homeo box 1pituitary otx-related factorSH3 domain-binding glutamic acid-rich-like protein 3SH3 domain binding glutamic acid-rich protein like 3SH3 domain-binding protein 1SH3BGRL3-like proteinTNF inhibitory proteinepididymis secretory protein Li 297
Modification date2018052320180519
UniProtAcc

P78337

Q9H299

Ensembl transtripts involved in fusion geneENST00000265340, ENST00000506438, 
ENST00000270792, ENST00000319041, 
Fusion gene scores* DoF score3 X 3 X 2=184 X 4 X 2=32
# samples 34
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: PITX1 [Title/Abstract] AND SH3BGRL3 [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
ChiTaRS3.1BF912850PITX1chr5

134367990

+SH3BGRL3chr1

26607655

+
* 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-3UTRENST00000265340ENST00000270792PITX1chr5

134367990

+SH3BGRL3chr1

26607655

+
intron-3UTRENST00000265340ENST00000319041PITX1chr5

134367990

+SH3BGRL3chr1

26607655

+
intron-3UTRENST00000506438ENST00000270792PITX1chr5

134367990

+SH3BGRL3chr1

26607655

+
intron-3UTRENST00000506438ENST00000319041PITX1chr5

134367990

+SH3BGRL3chr1

26607655

+

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FusionProtFeatures for PITX1_SH3BGRL3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PITX1

P78337

SH3BGRL3

Q9H299

Sequence-specific transcription factor that binds genepromoters and activates their transcription. May play a role inthe development of anterior structures, and in particular, thebrain and facies and in specifying the identity or structure ofhindlimb. {ECO:0000250|UniProtKB:P56673}. Could act as a modulator of glutaredoxin biologicalactivity.

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 PITX1_SH3BGRL3


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 PITX1_SH3BGRL3


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 PITX1_SH3BGRL3


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 PITX1_SH3BGRL3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePITX1C0004352Autistic Disorder1CTD_human
HgenePITX1C0009081Congenital clubfoot1CTD_human;HPO;ORPHANET;UNIPROT
HgenePITX1C1336708Testicular Germ Cell Tumor1CTD_human
TgeneSH3BGRL3C0023893Liver Cirrhosis, Experimental1CTD_human