![]() |
||||||
|
![]() | Fusion Gene Summary |
![]() | Fusion Gene ORF analysis |
![]() | Fusion Genomic Features |
![]() | Fusion Protein Features |
![]() | Fusion Gene Sequence |
![]() | Fusion Gene PPI analysis |
![]() | Related Drugs |
![]() | Related Diseases |
Fusion gene:FOXA3-CYP2C9 (FusionGDB2 ID:HG3171TG1559) |
Fusion Gene Summary for FOXA3-CYP2C9 |
![]() |
Fusion gene information | Fusion gene name: FOXA3-CYP2C9 | Fusion gene ID: hg3171tg1559 | Hgene | Tgene | Gene symbol | FOXA3 | CYP2C9 | Gene ID | 3171 | 1559 |
Gene name | forkhead box A3 | cytochrome P450 family 2 subfamily C member 9 | |
Synonyms | FKHH3|HNF3G|TCF3G | CPC9|CYP2C|CYP2C10|CYPIIC9|P450IIC9 | |
Cytomap | ('FOXA3')('CYP2C9') 19q13.32 | 10q23.33 | |
Type of gene | protein-coding | protein-coding | |
Description | hepatocyte nuclear factor 3-gammaHNF-3-gammaHNF-3GTCF-3Gfork head-related protein FKH H3forkhead box protein A3transcription factor 3G | cytochrome P450 2C9cytochrome P-450 S-mephenytoin 4-hydroxylasecytochrome P-450MPcytochrome P450 PB-1cytochrome P450, family 2, subfamily C, polypeptide 9flavoprotein-linked monooxygenasemicrosomal monooxygenasexenobiotic monooxygenase | |
Modification date | 20200313 | 20200313 | |
UniProtAcc | . | . | |
Ensembl transtripts involved in fusion gene | ENST00000302177, | ||
Fusion gene scores | * DoF score | 2 X 1 X 2=4 | 4 X 3 X 3=36 |
# samples | 2 | 4 | |
** MAII score | log2(2/4*10)=2.32192809488736 | log2(4/36*10)=0.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: FOXA3 [Title/Abstract] AND CYP2C9 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | FOXA3(46367783)-CYP2C9(96701614), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | FOXA3-CYP2C9 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. FOXA3-CYP2C9 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) |
![]() |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | FOXA3 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 12695546 |
Tgene | CYP2C9 | GO:0008210 | estrogen metabolic process | 12865317 |
Tgene | CYP2C9 | GO:0016098 | monoterpenoid metabolic process | 16401082 |
Tgene | CYP2C9 | GO:0017144 | drug metabolic process | 19219744|19651758 |
Tgene | CYP2C9 | GO:0019373 | epoxygenase P450 pathway | 7574697 |
Tgene | CYP2C9 | GO:0019627 | urea metabolic process | 19029318 |
Tgene | CYP2C9 | GO:0032787 | monocarboxylic acid metabolic process | 19651758 |
Tgene | CYP2C9 | GO:0042738 | exogenous drug catabolic process | 18619574 |
Tgene | CYP2C9 | GO:0043603 | cellular amide metabolic process | 19651758 |
Tgene | CYP2C9 | GO:0046456 | icosanoid biosynthetic process | 15766564 |
Tgene | CYP2C9 | GO:0055114 | oxidation-reduction process | 16401082|19219744 |
Tgene | CYP2C9 | GO:0070989 | oxidative demethylation | 18619574 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
![]() |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
![]() |
![]() * 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. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | STAD | TCGA-VQ-A923 | FOXA3 | chr19 | 46367783 | + | CYP2C9 | chr10 | 96701614 | + |
Top |
Fusion Gene ORF analysis for FOXA3-CYP2C9 |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
5CDS-3UTR | ENST00000302177 | ENST00000461906 | FOXA3 | chr19 | 46367783 | + | CYP2C9 | chr10 | 96701614 | + |
In-frame | ENST00000302177 | ENST00000260682 | FOXA3 | chr19 | 46367783 | + | CYP2C9 | chr10 | 96701614 | + |
![]() |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000302177 | FOXA3 | chr19 | 46367783 | + | ENST00000260682 | CYP2C9 | chr10 | 96701614 | + | 1933 | 266 | 197 | 1570 | 457 |
![]() |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000302177 | ENST00000260682 | FOXA3 | chr19 | 46367783 | + | CYP2C9 | chr10 | 96701614 | + | 0.001344861 | 0.9986551 |
Top |
Fusion Genomic Features for FOXA3-CYP2C9 |
![]() |
Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
FOXA3 | chr19 | 46367783 | + | CYP2C9 | chr10 | 96701614 | + | 6.95E-05 | 0.9999305 |
FOXA3 | chr19 | 46367783 | + | CYP2C9 | chr10 | 96701614 | + | 6.95E-05 | 0.9999305 |
![]() |
![]() |
![]() |
![]() |
Top |
Fusion Protein Features for FOXA3-CYP2C9 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr19:46367783/chr10:96701614) - 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. |
![]() |
![]() |
Hgene | Tgene |
. | . |
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. | FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. |
![]() * 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. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | FOXA3 | chr19:46367783 | chr10:96701614 | ENST00000302177 | + | 1 | 2 | 116_207 | 23 | 351.0 | DNA binding | Fork-head |
Top |
Fusion Gene Sequence for FOXA3-CYP2C9 |
![]() |
>31046_31046_1_FOXA3-CYP2C9_FOXA3_chr19_46367783_ENST00000302177_CYP2C9_chr10_96701614_ENST00000260682_length(transcript)=1933nt_BP=266nt GGAGCCCGGGGCGGGCGAGGGCGGGGGTGTCCCGGCTATAAAGCGTGGCCGCCTCCCGCGGCGCTCGGGACAGCCGTACCCCGGGCGGTC GGACGGGCGGGCGCCGGTGGGAGCTCGGGCCGTGCCCGCTGAGAGATCCAGAGCGCTCCGTTCCCCCGGGGCCGGAGCGGGGGCGGGTGG GGGCGTAAGCCCGGGGGATGCTGGGCTCAGTGAAGATGGAGGCCCATGACCTGGCCGAGTGGAGCTACTACCCGGAGGCGGGCGAGCTCT CAAAGGTCTATGGCCCTGTGTTCACTCTGTATTTTGGCCTGAAACCCATAGTGGTGCTGCATGGATATGAAGCAGTGAAGGAAGCCCTGA TTGATCTTGGAGAGGAGTTTTCTGGAAGAGGCATTTTCCCACTGGCTGAAAGAGCTAACAGAGGATTTGGAATTGTTTTCAGCAATGGAA AGAAATGGAAGGAGATCCGGCGTTTCTCCCTCATGACGCTGCGGAATTTTGGGATGGGGAAGAGGAGCATTGAGGACCGTGTTCAAGAGG AAGCCCGCTGCCTTGTGGAGGAGTTGAGAAAAACCAAGGCCTCACCCTGTGATCCCACTTTCATCCTGGGCTGTGCTCCCTGCAATGTGA TCTGCTCCATTATTTTCCATAAACGTTTTGATTATAAAGATCAGCAATTTCTTAACTTAATGGAAAAGTTGAATGAAAACATCAAGATTT TGAGCAGCCCCTGGATCCAGATCTGCAATAATTTTTCTCCTATCATTGATTACTTCCCGGGAACTCACAACAAATTACTTAAAAACGTTG CTTTTATGAAAAGTTATATTTTGGAAAAAGTAAAAGAACACCAAGAATCAATGGACATGAACAACCCTCAGGACTTTATTGATTGCTTCC TGATGAAAATGGAGAAGGAAAAGCACAACCAACCATCTGAATTTACTATTGAAAGCTTGGAAAACACTGCAGTTGACTTGTTTGGAGCTG GGACAGAGACGACAAGCACAACCCTGAGATATGCTCTCCTTCTCCTGCTGAAGCACCCAGAGGTCACAGCTAAAGTCCAGGAAGAGATTG AACGTGTGATTGGCAGAAACCGGAGCCCCTGCATGCAAGACAGGAGCCACATGCCCTACACAGATGCTGTGGTGCACGAGGTCCAGAGAT ACATTGACCTTCTCCCCACCAGCCTGCCCCATGCAGTGACCTGTGACATTAAATTCAGAAACTATCTCATTCCCAAGGGCACAACCATAT TAATTTCCCTGACTTCTGTGCTACATGACAACAAAGAATTTCCCAACCCAGAGATGTTTGACCCTCATCACTTTCTGGATGAAGGTGGCA ATTTTAAGAAAAGTAAATACTTCATGCCTTTCTCAGCAGGAAAACGGATTTGTGTGGGAGAAGCCCTGGCCGGCATGGAGCTGTTTTTAT TCCTGACCTCCATTTTACAGAACTTTAACCTGAAATCTCTGGTTGACCCAAAGAACCTTGACACCACTCCAGTTGTCAATGGATTTGCCT CTGTGCCGCCCTTCTACCAGCTGTGCTTCATTCCTGTCTGAAGAAGAGCAGATGGCCTGGCTGCTGCTGTGCAGTCCCTGCAGCTCTCTT TCCTCTGGGGCATTATCCATCTTTCACTATCTGTAATGCCTTTTCTCACCTGTCATCTCACATTTTCCCTTCCCTGAAGATCTAGTGAAC ATTCGACCTCCATTACGGAGAGTTTCCTATGTTTCACTGTGCAAATATATCTGCTATTCTCCATACTCTGTAACAGTTGCATTGACTGTC ACATAATGCTCATACTTATCTAATGTTGAGTTATTAATATGTTATTATTAAATAGAGAAATATGATTTGTGTATTATAATTCAAAGGCAT TTCTTTTCTGCATGTTCTAAATAAAAAGCATTATTATTTGCTG >31046_31046_1_FOXA3-CYP2C9_FOXA3_chr19_46367783_ENST00000302177_CYP2C9_chr10_96701614_ENST00000260682_length(amino acids)=457AA_BP=23 MLGSVKMEAHDLAEWSYYPEAGELSKVYGPVFTLYFGLKPIVVLHGYEAVKEALIDLGEEFSGRGIFPLAERANRGFGIVFSNGKKWKEI RRFSLMTLRNFGMGKRSIEDRVQEEARCLVEELRKTKASPCDPTFILGCAPCNVICSIIFHKRFDYKDQQFLNLMEKLNENIKILSSPWI QICNNFSPIIDYFPGTHNKLLKNVAFMKSYILEKVKEHQESMDMNNPQDFIDCFLMKMEKEKHNQPSEFTIESLENTAVDLFGAGTETTS TTLRYALLLLLKHPEVTAKVQEEIERVIGRNRSPCMQDRSHMPYTDAVVHEVQRYIDLLPTSLPHAVTCDIKFRNYLIPKGTTILISLTS VLHDNKEFPNPEMFDPHHFLDEGGNFKKSKYFMPFSAGKRICVGEALAGMELFLFLTSILQNFNLKSLVDPKNLDTTPVVNGFASVPPFY QLCFIPV -------------------------------------------------------------- |
Top |
Fusion Gene PPI Analysis for FOXA3-CYP2C9 |
![]() |
![]() |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Top |
Related Drugs for FOXA3-CYP2C9 |
![]() (DrugBank Version 5.1.8 2021-05-08) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Top |
Related Diseases for FOXA3-CYP2C9 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | FOXA3 | C0033578 | Prostatic Neoplasms | 1 | CTD_human |
Hgene | FOXA3 | C0376358 | Malignant neoplasm of prostate | 1 | CTD_human |
Tgene | C0019080 | Hemorrhage | 5 | CTD_human | |
Tgene | C0041696 | Unipolar Depression | 4 | PSYGENET | |
Tgene | C1269683 | Major Depressive Disorder | 4 | PSYGENET | |
Tgene | C0013221 | Drug toxicity | 3 | CTD_human | |
Tgene | C0019193 | Hepatitis, Toxic | 3 | CTD_human | |
Tgene | C0041755 | Adverse reaction to drug | 3 | CTD_human | |
Tgene | C0860207 | Drug-Induced Liver Disease | 3 | CTD_human | |
Tgene | C1262760 | Hepatitis, Drug-Induced | 3 | CTD_human | |
Tgene | C3658290 | Drug-Induced Acute Liver Injury | 3 | CTD_human | |
Tgene | C4277682 | Chemical and Drug Induced Liver Injury | 3 | CTD_human | |
Tgene | C4279912 | Chemically-Induced Liver Toxicity | 3 | CTD_human | |
Tgene | C0006118 | Brain Neoplasms | 1 | CTD_human | |
Tgene | C0013182 | Drug Allergy | 1 | CTD_human | |
Tgene | C0022660 | Kidney Failure, Acute | 1 | CTD_human | |
Tgene | C0027707 | Nephritis, Interstitial | 1 | CTD_human | |
Tgene | C0027765 | nervous system disorder | 1 | CTD_human | |
Tgene | C0030922 | Peptic Ulcer Hemorrhage | 1 | CTD_human | |
Tgene | C0033141 | Cardiomyopathies, Primary | 1 | CTD_human | |
Tgene | C0036529 | Myocardial Diseases, Secondary | 1 | CTD_human | |
Tgene | C0041349 | Nephritis, Tubulointerstitial | 1 | CTD_human | |
Tgene | C0153633 | Malignant neoplasm of brain | 1 | CTD_human | |
Tgene | C0496899 | Benign neoplasm of brain, unspecified | 1 | CTD_human | |
Tgene | C0750974 | Brain Tumor, Primary | 1 | CTD_human | |
Tgene | C0750977 | Recurrent Brain Neoplasm | 1 | CTD_human | |
Tgene | C0750979 | Primary malignant neoplasm of brain | 1 | CTD_human | |
Tgene | C0878544 | Cardiomyopathies | 1 | CTD_human | |
Tgene | C1527390 | Neoplasms, Intracranial | 1 | CTD_human | |
Tgene | C1565662 | Acute Kidney Insufficiency | 1 | CTD_human | |
Tgene | C2608079 | WARFARIN SENSITIVITY (disorder) | 1 | CTD_human | |
Tgene | C2609414 | Acute kidney injury | 1 | CTD_human |