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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:STRN-SULT6B1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: STRN-SULT6B1
FusionPDB ID: 87741
FusionGDB2.0 ID: 87741
HgeneTgene
Gene symbol

STRN

SULT6B1

Gene ID

6801

391365

Gene namestriatinsulfotransferase family 6B member 1
SynonymsPPP2R6A|SG2NA|STRN1ST6B1
Cytomap

2p22.2

2p22.2

Type of geneprotein-codingprotein-coding
Descriptionstriatinprotein phosphatase 2 regulatory subunit B'''alphastriatin, calmodulin binding proteinsulfotransferase 6B1sulfotransferase SULT6B1sulfotransferase family, cytosolic, 6B, member 1thyroxine sulfotransferase
Modification date2020031320200313
UniProtAcc

O43815

.
Ensembl transtripts involved in fusion geneENST idsENST00000263918, ENST00000379213, 
ENST00000407963, ENST00000260637, 
ENST00000379149, ENST00000535679, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 14 X 10=14001 X 1 X 1=1
# samples 151
** MAII scorelog2(15/1400*10)=-3.22239242133645
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context (manual curation of fusion genes in FusionPDB)

PubMed: STRN [Title/Abstract] AND SULT6B1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)STRN(37126666)-SULT6B1(37415690), # samples:3
Anticipated loss of major functional domain due to fusion event.STRN-SULT6B1 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.
STRN-SULT6B1 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

check buttonFusion gene breakpoints across STRN (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 SULT6B1 (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
ChimerDB4LIHCTCGA-NI-A4U2-01ASTRNchr2

37126666

-SULT6B1chr2

37415690

-


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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)
ENST00000263918STRNchr237126666-ENST00000260637SULT6B1chr237415690-173880491622537
ENST00000263918STRNchr237126666-ENST00000379149SULT6B1chr237415690-14268049881290
ENST00000263918STRNchr237126666-ENST00000535679SULT6B1chr237415690-17388049881290
ENST00000379213STRNchr237126666-ENST00000260637SULT6B1chr237415690-169375901577525
ENST00000379213STRNchr237126666-ENST00000379149SULT6B1chr237415690-13817590836278
ENST00000379213STRNchr237126666-ENST00000535679SULT6B1chr237415690-16937590836278

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
ENST00000263918ENST00000260637STRNchr237126666-SULT6B1chr237415690-0.0005309560.9994691
ENST00000263918ENST00000379149STRNchr237126666-SULT6B1chr237415690-0.0005566540.99944335
ENST00000263918ENST00000535679STRNchr237126666-SULT6B1chr237415690-0.000488480.9995115
ENST00000379213ENST00000260637STRNchr237126666-SULT6B1chr237415690-0.0004661290.9995339
ENST00000379213ENST00000379149STRNchr237126666-SULT6B1chr237415690-0.0005753540.9994247
ENST00000379213ENST00000535679STRNchr237126666-SULT6B1chr237415690-0.0005175370.9994824

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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

>87741_87741_1_STRN-SULT6B1_STRN_chr2_37126666_ENST00000263918_SULT6B1_chr2_37415690_ENST00000260637_length(amino acids)=537AA_BP=265
MDEQAGPGVFFSNNHPGAGGAKGLGPLAEAAAAGDGAAAAGAARAQYSLPGILHFLQHEWARFEVERAQWEVERAELQAQIAFLQGERKG
QENLKKDLVRRIKMLEYALKQERAKYHKLKYGTELNQGDMKPPSYDSDEGNETEVQPQQNSQLMWKQGRQLLRQYLQEVGYTDTILDVKS
KRVRALLGFSSDVTDREDDKNQDSVVNGTEAEVKETAMIAKSELTDSASVLDNFKFLESAAADFSDEDEDDDVDGREKSVIDTSTGIPYP
ITMCTSETFQALDTFEARHDDIVLASYPKCGSNWILHIVSELIYAVSKKKYKYPEFPVLECGDSEKYQRMKGFPSPRILATHLHYDKLPG
SIFENKAKILVIFRNPKDTAVSFLHFHNDVPDIPSYGSWDEFFRQFMKGQVSWGRYFDFAINWNKHLDGDNVKFILYEDLKENLAAGIKQ

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

>87741_87741_2_STRN-SULT6B1_STRN_chr2_37126666_ENST00000263918_SULT6B1_chr2_37415690_ENST00000379149_length(amino acids)=290AA_BP=
MDEQAGPGVFFSNNHPGAGGAKGLGPLAEAAAAGDGAAAAGAARAQYSLPGILHFLQHEWARFEVERAQWEVERAELQAQIAFLQGERKG
QENLKKDLVRRIKMLEYALKQERAKYHKLKYGTELNQGDMKPPSYDSDEGNETEVQPQQNSQLMWKQGRQLLRQYLQEVGYTDTILDVKS
KRVRALLGFSSDVTDREDDKNQDSVVNGTEAEVKETAMIAKSELTDSASVLDNFKFLESAAADFSDEDEDDDVDGREKSVIDTSTVKLVI

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

>87741_87741_3_STRN-SULT6B1_STRN_chr2_37126666_ENST00000263918_SULT6B1_chr2_37415690_ENST00000535679_length(amino acids)=290AA_BP=
MDEQAGPGVFFSNNHPGAGGAKGLGPLAEAAAAGDGAAAAGAARAQYSLPGILHFLQHEWARFEVERAQWEVERAELQAQIAFLQGERKG
QENLKKDLVRRIKMLEYALKQERAKYHKLKYGTELNQGDMKPPSYDSDEGNETEVQPQQNSQLMWKQGRQLLRQYLQEVGYTDTILDVKS
KRVRALLGFSSDVTDREDDKNQDSVVNGTEAEVKETAMIAKSELTDSASVLDNFKFLESAAADFSDEDEDDDVDGREKSVIDTSTVKLVI

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

>87741_87741_4_STRN-SULT6B1_STRN_chr2_37126666_ENST00000379213_SULT6B1_chr2_37415690_ENST00000260637_length(amino acids)=525AA_BP=253
MDEQAGPGVFFSNNHPGAGGAKGLGPLAGAARAQYSLPGILHFLQHEWARFEVERAQWEVERAELQAQIAFLQGERKGQENLKKDLVRRI
KMLEYALKQERAKYHKLKYGTELNQGDMKPPSYDSDEGNETEVQPQQNSQLMWKQGRQLLRQYLQEVGYTDTILDVKSKRVRALLGFSSD
VTDREDDKNQDSVVNGTEAEVKETAMIAKSELTDSASVLDNFKFLESAAADFSDEDEDDDVDGREKSVIDTSTGIPYPITMCTSETFQAL
DTFEARHDDIVLASYPKCGSNWILHIVSELIYAVSKKKYKYPEFPVLECGDSEKYQRMKGFPSPRILATHLHYDKLPGSIFENKAKILVI
FRNPKDTAVSFLHFHNDVPDIPSYGSWDEFFRQFMKGQVSWGRYFDFAINWNKHLDGDNVKFILYEDLKENLAAGIKQIAEFLGFFLTGE

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

>87741_87741_5_STRN-SULT6B1_STRN_chr2_37126666_ENST00000379213_SULT6B1_chr2_37415690_ENST00000379149_length(amino acids)=278AA_BP=
MDEQAGPGVFFSNNHPGAGGAKGLGPLAGAARAQYSLPGILHFLQHEWARFEVERAQWEVERAELQAQIAFLQGERKGQENLKKDLVRRI
KMLEYALKQERAKYHKLKYGTELNQGDMKPPSYDSDEGNETEVQPQQNSQLMWKQGRQLLRQYLQEVGYTDTILDVKSKRVRALLGFSSD
VTDREDDKNQDSVVNGTEAEVKETAMIAKSELTDSASVLDNFKFLESAAADFSDEDEDDDVDGREKSVIDTSTVKLVIGKICSVKFRTRK

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

>87741_87741_6_STRN-SULT6B1_STRN_chr2_37126666_ENST00000379213_SULT6B1_chr2_37415690_ENST00000535679_length(amino acids)=278AA_BP=
MDEQAGPGVFFSNNHPGAGGAKGLGPLAGAARAQYSLPGILHFLQHEWARFEVERAQWEVERAELQAQIAFLQGERKGQENLKKDLVRRI
KMLEYALKQERAKYHKLKYGTELNQGDMKPPSYDSDEGNETEVQPQQNSQLMWKQGRQLLRQYLQEVGYTDTILDVKSKRVRALLGFSSD
VTDREDDKNQDSVVNGTEAEVKETAMIAKSELTDSASVLDNFKFLESAAADFSDEDEDDDVDGREKSVIDTSTVKLVIGKICSVKFRTRK

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

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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/chr2:37126666/chr2:37415690)
- 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
STRN

O43815

.
FUNCTION: Calmodulin-binding protein which may function as scaffolding or signaling protein and may play a role in dendritic Ca(2+) signaling.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.

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
HgeneSTRNchr2:37126666chr2:37415690ENST00000263918-61853_120265.0781.0Coiled coilOntology_term=ECO:0000255
HgeneSTRNchr2:37126666chr2:37415690ENST00000379213-71853_120253.0732.0Coiled coilOntology_term=ECO:0000255
HgeneSTRNchr2:37126666chr2:37415690ENST00000263918-618149_166265.0781.0RegionCalmodulin-binding
HgeneSTRNchr2:37126666chr2:37415690ENST00000263918-61855_63265.0781.0RegionCaveolin-binding
HgeneSTRNchr2:37126666chr2:37415690ENST00000379213-718149_166253.0732.0RegionCalmodulin-binding
HgeneSTRNchr2:37126666chr2:37415690ENST00000379213-71855_63253.0732.0RegionCaveolin-binding
TgeneSULT6B1chr2:37126666chr2:37415690ENST00000260637-17237_24228.333333333333332266.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST00000260637-17259_26128.333333333333332266.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST00000260637-1765_7028.333333333333332266.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST0000037914904237_2420.0200.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST0000037914904259_2610.0200.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST000003791490465_700.0200.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST0000040796308237_2420266.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST0000040796308259_2610266.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST000004079630865_700266.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST0000053567907237_2420.0304.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST0000053567907259_2610.0304.0Nucleotide bindingPAPS
TgeneSULT6B1chr2:37126666chr2:37415690ENST000005356790765_700.0304.0Nucleotide bindingPAPS

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSTRNchr2:37126666chr2:37415690ENST00000263918-618461_500265.0781.0RepeatNote=WD 1
HgeneSTRNchr2:37126666chr2:37415690ENST00000263918-618514_553265.0781.0RepeatNote=WD 2
HgeneSTRNchr2:37126666chr2:37415690ENST00000263918-618567_606265.0781.0RepeatNote=WD 3
HgeneSTRNchr2:37126666chr2:37415690ENST00000263918-618662_701265.0781.0RepeatNote=WD 4
HgeneSTRNchr2:37126666chr2:37415690ENST00000263918-618704_743265.0781.0RepeatNote=WD 5
HgeneSTRNchr2:37126666chr2:37415690ENST00000263918-618750_779265.0781.0RepeatNote=WD 6
HgeneSTRNchr2:37126666chr2:37415690ENST00000379213-718461_500253.0732.0RepeatNote=WD 1
HgeneSTRNchr2:37126666chr2:37415690ENST00000379213-718514_553253.0732.0RepeatNote=WD 2
HgeneSTRNchr2:37126666chr2:37415690ENST00000379213-718567_606253.0732.0RepeatNote=WD 3
HgeneSTRNchr2:37126666chr2:37415690ENST00000379213-718662_701253.0732.0RepeatNote=WD 4
HgeneSTRNchr2:37126666chr2:37415690ENST00000379213-718704_743253.0732.0RepeatNote=WD 5
HgeneSTRNchr2:37126666chr2:37415690ENST00000379213-718750_779253.0732.0RepeatNote=WD 6


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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
STRNSTK24, MCC, CTTNBP2, CTTNBP2NL, STRIP1, MOB4, PDCD10, PPP2CA, PPP2R1A, STK26, SIKE1, STK25, STRN3, PPP2R1B, STRN4, STRIP2, SLMAP, CCT2, CCT8, CCT3, TCP1, CCT5, FGFR1OP2, CCT6A, CCT7, CCT4, CCT6B, TRAF3IP3, PPP2CB, ZRANB1, Dynll1, ELAVL1, LNX1, APC, TJP1, DDX1, DYNC1H1, CPSF6, EIF2S1, SF3B5, BRCA1, ECT2, PAXIP1, STK3, STK4, TFIP11, RINT1, PCOLCE2, LYPD3, NR1H3, PPP2R2C, RASSF3, PGAM5, NTRK1, HSPB1, DYNLL1, MAP4K4, EEF1E1, BAG2, SLC43A3, AHNAK, Ppp2ca, Ppp2r1a, Strn3, Arrb2, Strip1, PRDM14, TNFRSF1A, NHSL2, PSMC5, PLP1, ZNF550, SNX24, LRRCC1, ZNF331, PRPF19, SPINK2, EXOC1, PKN3, NCKAP5L, TFPT, CCHCR1, YEATS4, TUFT1, RABGAP1L, GOLGA5, GIPC1, ESR2, USP15, GOLGA2, KIAA1429, ATG16L1, HOOK3, EP300, ESR1, RMDN3, CUL4A, TULP3, GOLGA1, TMOD1, MINK1, TNIK, SMAD4, DYNLL2, PMF1, RABEP2, ENDOD1, FLII, KIAA1522, GOLGA8G, ISCA2, GOLGA6A, FILIP1, SSUH2, PCM1, CAMK2B, MAP1S,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
STRNall structure
SULT6B1


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 STRN-SULT6B1


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 STRN-SULT6B1


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