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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:STK11-BSG

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: STK11-BSG
FusionPDB ID: 87445
FusionGDB2.0 ID: 87445
HgeneTgene
Gene symbol

STK11

BSG

Gene ID

6794

682

Gene nameserine/threonine kinase 11basigin (Ok blood group)
SynonymsLKB1|PJS|hLKB15F7|CD147|EMMPRIN|EMPRIN|OK|SLC7A11|TCSF
Cytomap

19p13.3

19p13.3

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase STK11liver kinase B1polarization-related protein LKB1renal carcinoma antigen NY-REN-19serine/threonine-protein kinase 11serine/threonine-protein kinase LKB1basiginOK blood group antigencollagenase stimulatory factorextracellular matrix metalloproteinase inducerleukocyte activation antigen M6tumor cell-derived collagenase stimulatory factor
Modification date2020032920200315
UniProtAcc.

P35613

Ensembl transtripts involved in fusion geneENST idsENST00000326873, ENST00000585748, 
ENST00000574970, ENST00000333511, 
ENST00000353555, ENST00000545507, 
ENST00000346916, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 3 X 8=3129 X 12 X 6=648
# samples 1714
** MAII scorelog2(17/312*10)=-0.876011282724546
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/648*10)=-2.21056698593966
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: STK11 [Title/Abstract] AND BSG [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)STK11(1207202)-BSG(580379), # samples:2
Anticipated loss of major functional domain due to fusion event.STK11-BSG seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
STK11-BSG seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
STK11-BSG seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
STK11-BSG seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
* 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
HgeneSTK11

GO:0006468

protein phosphorylation

12805220|25329316

HgeneSTK11

GO:0007050

cell cycle arrest

12805220|17216128

HgeneSTK11

GO:0046777

protein autophosphorylation

11430832

HgeneSTK11

GO:0071493

cellular response to UV-B

25329316

HgeneSTK11

GO:0072332

intrinsic apoptotic signaling pathway by p53 class mediator

11430832


check buttonFusion gene breakpoints across STK11 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across BSG (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4STADTCGA-BR-8289-01ASTK11chr19

1207202

+BSGchr19

579500

+
ChimerDB4STADTCGA-BR-8289-01ASTK11chr19

1207202

+BSGchr19

580379

+
ChimerDB4STADTCGA-BR-8289STK11chr19

1207202

+BSGchr19

579499

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000326873STK11chr191207202+ENST00000346916BSGchr19580379+2798146312762425

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000326873ENST00000346916STK11chr191207202+BSGchr19580379+0.0021925440.99780744

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>87445_87445_1_STK11-BSG_STK11_chr19_1207202_ENST00000326873_BSG_chr19_580379_ENST00000346916_length(amino acids)=425AA_BP=127
MTSVESMRWMNVSIPTDISSPSVNMPSCCGSTTSMLDPGSWSPAASPESAGERSFLVFRLPFSKILQRKKKKKRQQKPQKEGKNPSSNRN
DCSTRQSRLRVQARCRVCGPAGTGGPGRRLRREFQWDPGLRTGRRPGQGQLRPRGPWGGRPGLFSARSSSGDLRPTDKYEHGRAQSSPGR
PSHRPGPRRRYPPGPPHLESPTSLGASPATPRSHRLSQEQTLRRGRPSGPPGGRRLPPARASVRGAGGVREASRRGQQLRSGLVAARRPR
GPALGAPRAGPRPPRWSPGPGRRPPPRKRLPERAPRPECPQRPVRGAARRRGLHGAPGGRGGAGRRLRAGGFPKVPGPGRRVPLAAAAAR

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr19:1207202/chr19:580379)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

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

P35613

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: [Isoform 1]: Essential for normal retinal maturation and development (By similarity). Acts as a retinal cell surface receptor for NXNL1 and plays an important role in NXNL1-mediated survival of retinal cone photoreceptors (PubMed:25957687). In association with glucose transporter SLC16A1/GLUT1 and NXNL1, promotes retinal cone survival by enhancing aerobic glycolysis and accelerating the entry of glucose into photoreceptors (PubMed:25957687). May act as a potent stimulator of IL6 secretion in multiple cell lines that include monocytes (PubMed:21620857). {ECO:0000250|UniProtKB:P18572, ECO:0000269|PubMed:21620857, ECO:0000269|PubMed:25957687}.; FUNCTION: [Isoform 2]: Signaling receptor for cyclophilins, essential for PPIA/CYPA and PPIB/CYPB-dependent signaling related to chemotaxis and adhesion of immune cells (PubMed:11943775, PubMed:11688976). Plays an important role in targeting monocarboxylate transporters SLC16A1/GLUT1, SLC16A11 and SLC16A12 to the plasma membrane (PubMed:17127621, PubMed:21778275, PubMed:28666119). Acts as a coreceptor for vascular endothelial growth factor receptor 2 (KDR/VEGFR2) in endothelial cells enhancing its VEGFA-mediated activation and downstream signaling (PubMed:25825981). Promotes angiogenesis through EPAS1/HIF2A-mediated up-regulation of VEGFA (isoform VEGF-165 and VEGF-121) and KDR/VEGFR2 in endothelial cells (PubMed:19837976). Plays a key role in regulating tumor growth, invasion, metastasis and neoangiogenesis by stimulating the production and release of extracellular matrix metalloproteinases and KDR/VEGFR2 by both tumor cells and stromal cells (fibroblasts and endothelial cells) (PubMed:12553375, PubMed:11992541, PubMed:15833850). {ECO:0000269|PubMed:11688976, ECO:0000269|PubMed:11943775, ECO:0000269|PubMed:11992541, ECO:0000269|PubMed:12553375, ECO:0000269|PubMed:15833850, ECO:0000269|PubMed:17127621, ECO:0000269|PubMed:19837976, ECO:0000269|PubMed:21778275, ECO:0000269|PubMed:25825981, ECO:0000269|PubMed:28666119}.; FUNCTION: [Isoform 1]: (Microbial infection) Erythrocyte receptor for P.falciparum RH5 which is essential for erythrocyte invasion by the merozoite stage of P.falciparum isolates 3D7 and Dd2. {ECO:0000269|PubMed:22080952}.; FUNCTION: [Isoform 2]: (Microbial infection) Erythrocyte receptor for P.falciparum RH5 which is essential for erythrocyte invasion by the merozoite stage of P.falciparum isolates 3D7, Dd2, 7G8 and HB3 (PubMed:22080952, PubMed:26195724). Binding of P.falciparum RH5 results in BSG dimerization which triggers an increase in intracellular Ca(2+) in the erythrocyte (PubMed:28409866). This essential step leads to a rearrangement of the erythrocyte cytoskeleton required for the merozoite invasion (PubMed:28409866). {ECO:0000269|PubMed:22080952, ECO:0000269|PubMed:26195724, ECO:0000269|PubMed:28409866}.; FUNCTION: [Isoform 2]: (Microbial infection) Can facilitate human SARS coronavirus (SARS-CoV-1) infection via its interaction with virus-associated PPIA/CYPA. {ECO:0000269|PubMed:15688292}.; FUNCTION: [Isoform 2]: (Microbial infection) Can facilitate HIV-1 infection via its interaction with virus-associated PPIA/CYPA. {ECO:0000269|PubMed:11353871}.; FUNCTION: [Isoform 2]: (Microbial infection) First described as a receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), it is not required for SARS-CoV-2 infection. {ECO:0000269|PubMed:33432067, ECO:0000303|PubMed:32307653}.; FUNCTION: [Isoform 2]: (Microbial infection) Acts as a receptor for measles virus. {ECO:0000269|PubMed:20147391}.; FUNCTION: [Isoform 2]: (Microbial infection) Promotes entry of pentamer-expressing human cytomegalovirus (HCMV) into epithelial and endothelial cells. {ECO:0000269|PubMed:29739904}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSTK11chr19:1207202chr19:580379ENST00000326873+11055_6396.66666666666667225.33333333333334Nucleotide bindingATP
TgeneBSGchr19:1207202chr19:580379ENST0000033351129356_359190.66666666666666587.3333333333334Compositional biasNote=Poly-Asp
TgeneBSGchr19:1207202chr19:580379ENST0000034691607356_35910.666666666666666359.6666666666667Compositional biasNote=Poly-Asp
TgeneBSGchr19:1207202chr19:580379ENST0000035355518356_35974.66666666666667476.6666666666667Compositional biasNote=Poly-Asp
TgeneBSGchr19:1207202chr19:580379ENST0000054550718356_3590333.3333333333333Compositional biasNote=Poly-Asp
TgeneBSGchr19:1207202chr19:580379ENST0000033351129221_315190.66666666666666587.3333333333334DomainIg-like V-type
TgeneBSGchr19:1207202chr19:580379ENST0000034691607138_21910.666666666666666359.6666666666667DomainIg-like C2-type
TgeneBSGchr19:1207202chr19:580379ENST0000034691607221_31510.666666666666666359.6666666666667DomainIg-like V-type
TgeneBSGchr19:1207202chr19:580379ENST000003469160737_12010.666666666666666359.6666666666667DomainIg-like
TgeneBSGchr19:1207202chr19:580379ENST0000035355518138_21974.66666666666667476.6666666666667DomainIg-like C2-type
TgeneBSGchr19:1207202chr19:580379ENST0000035355518221_31574.66666666666667476.6666666666667DomainIg-like V-type
TgeneBSGchr19:1207202chr19:580379ENST0000054550718138_2190333.3333333333333DomainIg-like C2-type
TgeneBSGchr19:1207202chr19:580379ENST0000054550718221_3150333.3333333333333DomainIg-like V-type
TgeneBSGchr19:1207202chr19:580379ENST000005455071837_1200333.3333333333333DomainIg-like
TgeneBSGchr19:1207202chr19:580379ENST0000033351129345_385190.66666666666666587.3333333333334Topological domainCytoplasmic
TgeneBSGchr19:1207202chr19:580379ENST0000034691607138_32310.666666666666666359.6666666666667Topological domainExtracellular
TgeneBSGchr19:1207202chr19:580379ENST0000034691607345_38510.666666666666666359.6666666666667Topological domainCytoplasmic
TgeneBSGchr19:1207202chr19:580379ENST0000035355518138_32374.66666666666667476.6666666666667Topological domainExtracellular
TgeneBSGchr19:1207202chr19:580379ENST0000035355518345_38574.66666666666667476.6666666666667Topological domainCytoplasmic
TgeneBSGchr19:1207202chr19:580379ENST0000054550718138_3230333.3333333333333Topological domainExtracellular
TgeneBSGchr19:1207202chr19:580379ENST0000054550718345_3850333.3333333333333Topological domainCytoplasmic
TgeneBSGchr19:1207202chr19:580379ENST0000033351129324_344190.66666666666666587.3333333333334TransmembraneHelical
TgeneBSGchr19:1207202chr19:580379ENST0000034691607324_34410.666666666666666359.6666666666667TransmembraneHelical
TgeneBSGchr19:1207202chr19:580379ENST0000035355518324_34474.66666666666667476.6666666666667TransmembraneHelical
TgeneBSGchr19:1207202chr19:580379ENST0000054550718324_3440333.3333333333333TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSTK11chr19:1207202chr19:580379ENST00000326873+11049_30996.66666666666667225.33333333333334DomainProtein kinase
TgeneBSGchr19:1207202chr19:580379ENST0000033351129138_219190.66666666666666587.3333333333334DomainIg-like C2-type
TgeneBSGchr19:1207202chr19:580379ENST000003335112937_120190.66666666666666587.3333333333334DomainIg-like
TgeneBSGchr19:1207202chr19:580379ENST000003535551837_12074.66666666666667476.6666666666667DomainIg-like
TgeneBSGchr19:1207202chr19:580379ENST0000033351129138_323190.66666666666666587.3333333333334Topological domainExtracellular


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
STK11
BSG


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to STK11-BSG


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to STK11-BSG


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource