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![]() | 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:DHX34-SAE1 (FusionGDB2 ID:HG9704TG10055) |
Fusion Gene Summary for DHX34-SAE1 |
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Fusion gene information | Fusion gene name: DHX34-SAE1 | Fusion gene ID: hg9704tg10055 | Hgene | Tgene | Gene symbol | DHX34 | SAE1 | Gene ID | 9704 | 10055 |
Gene name | DExH-box helicase 34 | SUMO1 activating enzyme subunit 1 | |
Synonyms | DDX34|HRH1 | AOS1|HSPC140|SUA1|UBLE1A | |
Cytomap | ('DHX34')('SAE1') 19q13.32 | 19q13.32 | |
Type of gene | protein-coding | protein-coding | |
Description | probable ATP-dependent RNA helicase DHX34DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 34DEAH (Asp-Glu-Ala-His) box polypeptide 34DEAH box protein 34DEAH-box helicase 34probable ATP-dependent helicase DHX34 | SUMO-activating enzyme subunit 1SUMO-1 activating enzyme E1 N subunitSUMO-1 activating enzyme subunit 1activator of SUMO1sentrin/SUMO-activating protein AOS1ubiquitin-like 1-activating enzyme E1Aubiquitin-like protein SUMO-1 activating enzyme | |
Modification date | 20200322 | 20200313 | |
UniProtAcc | . | . | |
Ensembl transtripts involved in fusion gene | ENST00000328771, ENST00000471451, | ||
Fusion gene scores | * DoF score | 5 X 5 X 4=100 | 9 X 8 X 10=720 |
# samples | 5 | 13 | |
** MAII score | log2(5/100*10)=-1 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(13/720*10)=-2.46948528330122 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: DHX34 [Title/Abstract] AND SAE1 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | DHX34(47865950)-SAE1(47712416), # samples:4 | ||
Anticipated loss of major functional domain due to fusion event. | DHX34-SAE1 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. DHX34-SAE1 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. DHX34-SAE1 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. DHX34-SAE1 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. DHX34-SAE1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | SAE1 | GO:0016925 | protein sumoylation | 15660128|20164921 |
Tgene | SAE1 | GO:0033235 | positive regulation of protein sumoylation | 10187858 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * 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 | UCEC | TCGA-5B-A90C-01A | DHX34 | chr19 | 47865950 | - | SAE1 | chr19 | 47712416 | + |
ChimerDB4 | UCEC | TCGA-5B-A90C-01A | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
ChimerDB4 | UCEC | TCGA-5B-A90C | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
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Fusion Gene ORF analysis for DHX34-SAE1 |
![]() * 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 | ENST00000328771 | ENST00000392776 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
Frame-shift | ENST00000328771 | ENST00000270225 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
Frame-shift | ENST00000328771 | ENST00000413379 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
Frame-shift | ENST00000328771 | ENST00000598840 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
In-frame | ENST00000328771 | ENST00000540850 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
intron-3CDS | ENST00000471451 | ENST00000270225 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
intron-3CDS | ENST00000471451 | ENST00000413379 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
intron-3CDS | ENST00000471451 | ENST00000540850 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
intron-3CDS | ENST00000471451 | ENST00000598840 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
intron-3UTR | ENST00000471451 | ENST00000392776 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + |
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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) |
ENST00000328771 | DHX34 | chr19 | 47865950 | + | ENST00000540850 | SAE1 | chr19 | 47712416 | + | 2152 | 1942 | 322 | 2034 | 570 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000328771 | ENST00000540850 | DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712416 | + | 0.016982205 | 0.9830178 |
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Fusion Genomic Features for DHX34-SAE1 |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712415 | + | 2.32E-07 | 0.99999976 |
DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712415 | + | 2.32E-07 | 0.99999976 |
DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712415 | + | 2.32E-07 | 0.99999976 |
DHX34 | chr19 | 47865950 | + | SAE1 | chr19 | 47712415 | + | 2.32E-07 | 0.99999976 |
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Fusion Protein Features for DHX34-SAE1 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr19:47865950/chr19:47712416) - 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. |
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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 |
Hgene | DHX34 | chr19:47865950 | chr19:47712416 | ENST00000328771 | + | 6 | 17 | 172_332 | 531 | 1144.0 | Domain | Helicase ATP-binding |
Hgene | DHX34 | chr19:47865950 | chr19:47712416 | ENST00000328771 | + | 6 | 17 | 279_282 | 531 | 1144.0 | Motif | Note=DEAH box |
Hgene | DHX34 | chr19:47865950 | chr19:47712416 | ENST00000328771 | + | 6 | 17 | 185_192 | 531 | 1144.0 | Nucleotide binding | ATP |
- 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 | DHX34 | chr19:47865950 | chr19:47712416 | ENST00000328771 | + | 6 | 17 | 368_536 | 531 | 1144.0 | Domain | Helicase C-terminal |
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Fusion Gene Sequence for DHX34-SAE1 |
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>22670_22670_1_DHX34-SAE1_DHX34_chr19_47865950_ENST00000328771_SAE1_chr19_47712416_ENST00000540850_length(transcript)=2152nt_BP=1942nt ACGAGATGGCTGTGTGCGCAGGCGCAAGACTAGCGCTCTTGGGACCGGAAGTTAAGGCGTTCGCGGCGTGTGAATCCAGGGCCTGAAAAC CCAGAATGAACTTGTGTCCATCCCAGAGATCACTGCAGATGTCATGAGGTACCCTTTGTGTCACCAGCTCAAGCAGGCCTCTGGCCACTT TATCATCTGTGGTGGTCCTGTGCCGTGACCAGGAGGAAAAATTAGCTCTTTGAAGAGAAAGTAGTTCTCTATTGCAGGCACTGGCCTCTT AAATTGTTGCAGGTGGGGAATGGATGAGAATATTTGTTTTGGGTGATCAGAACTGAGACTCCTATTGTGGATTAGTAACATGCCTCCTCC TAGAACAAGGGAGGGCAGGGATCGCCGAGACCACCACCGGGCTCCCAGCGAGGAAGAGGCCTTGGAGAAATGGGACTGGAATTGTCCAGA GACGCGTCGCCTCTTGGAAGATGCCTTCTTCCGTGAAGAGGATTACATCCGTCAGGGTTCTGAGGAATGTCAGAAGTTTTGGACCTTCTT TGAACGCCTGCAGAGATTCCAGAATCTCAAGACCTCCAGGAAGGAGGAGAAAGACCCTGGACAGCCCAAGCACAGCATCCCAGCGCTGGC CGACCTACCTCGCACTTACGACCCACGTTACCGCATCAACCTCTCTGTTCTTGGCCCTGCCACGCGGGGCTCTCAGGGACTGGGCAGGCA CTTGCCCGCGGAGAGAGTGGCTGAGTTCCGCCGAGCCCTGTTGCACTACCTGGACTTTGGCCAGAAGCAGGCATTTGGGCGTCTGGCCAA GCTGCAGCGTGAGCGGGCAGCCCTCCCCATCGCCCAGTATGGGAACCGCATCCTGCAGACGCTGAAGGAGCACCAGGTGGTGGTAGTGGC CGGTGACACCGGCTGTGGCAAGTCCACTCAGGTGCCCCAGTACCTGCTGGCTGCTGGCTTCAGTCATGTGGCGTGCACCCAGCCCCGGCG GATCGCCTGCATCTCACTGGCCAAGCGTGTGGGCTTTGAGAGCCTCAGTCAGTATGGCTCACAGGTCGGCTACCAGATCCGCTTTGAGAG CACACGTTCGGCGGCCACCAAGATTGTATTCCTGACAGTGGGGCTGCTCCTGCGACAAATCCAGCGGGAACCCAGCCTGCCCCAGTATGA GGTCCTGATTGTGGATGAAGTCCATGAGCGGCATCTCCACAACGATTTCCTCCTGGGCGTCCTCCAGCGCCTGTTGCCCACGCGGCCTGA CCTCAAGGTCATCCTCATGTCGGCCACCATCAACATCTCGCTCTTCTCCAGCTATTTCAGCAATGCCCCTGTGGTACAGGTGCCTGGGAG GCTGTTCCCCATCACGGTTGTGTACCAGCCGCAGGAGGCGGAGCCGACCACGTCCAAGTCAGAGAAGCTGGACCCGCGGCCTTTCCTGAG GGTGCTGGAGTCCATTGACCACAAGTACCCGCCTGAGGAGCGGGGTGACCTCCTCGTCTTCCTCAGCGGCATGGCGGAGATCAGCGCCGT GCTGGAGGCTGCCCAGACCTATGCCAGCCACACCCAGCGCTGGGTGGTACTGCCACTGCACAGCGCCCTGTCTGTGGCCGACCAGGACAA GGTATTTGATGTGGCACCCCCTGGAGTCCGGAAATGCATCCTCTCCACCAACATTGCTGAGACCTCAGTCACCATTGACGGGATCCGCTT CGTAGTAGATTCCGGAAAGGTGAAGGAGATGAGCTACGATCCGCAGGCCAAGCTGCAACGGCTGCAGGAGTTCTGGATTAGTCAGGCCAG CGCAGAGCAGCGGAAGGGCCGGGCGGGCCGCACGGGCCCCGGAGTCTGCTTCCGCCTCTATGCCGAATCGGACTATGATGCCTTCGCCCC CTACCCCGTCCCAGAAATTCGGAGGGTGGCCCTGGACTCGTTGGTGCTGCAGGCCCTGTCTCAGCGGGACCCTCCTCACAACAACTTCTT CTTCTTCGATGGCATGAAGGGGAATGGGATTGTGGAGTGCCTTGGCCCCAAGTGAACTCAAGATTTGGCAGCCCCAGAGATGCCAACTGC AGCATGCCCACCTGTATTCCCTGTCCCCTTCCTTCATGAAGGCATCTCCAGGCAAGGAAAACTGAAGTCATTGGCCCGATAC >22670_22670_1_DHX34-SAE1_DHX34_chr19_47865950_ENST00000328771_SAE1_chr19_47712416_ENST00000540850_length(amino acids)=570AA_BP=539 MRLLLWISNMPPPRTREGRDRRDHHRAPSEEEALEKWDWNCPETRRLLEDAFFREEDYIRQGSEECQKFWTFFERLQRFQNLKTSRKEEK DPGQPKHSIPALADLPRTYDPRYRINLSVLGPATRGSQGLGRHLPAERVAEFRRALLHYLDFGQKQAFGRLAKLQRERAALPIAQYGNRI LQTLKEHQVVVVAGDTGCGKSTQVPQYLLAAGFSHVACTQPRRIACISLAKRVGFESLSQYGSQVGYQIRFESTRSAATKIVFLTVGLLL RQIQREPSLPQYEVLIVDEVHERHLHNDFLLGVLQRLLPTRPDLKVILMSATINISLFSSYFSNAPVVQVPGRLFPITVVYQPQEAEPTT SKSEKLDPRPFLRVLESIDHKYPPEERGDLLVFLSGMAEISAVLEAAQTYASHTQRWVVLPLHSALSVADQDKVFDVAPPGVRKCILSTN IAETSVTIDGIRFVVDSGKVKEMSYDPQAKLQRLQEFWISQASAEQRKGRAGRTGPGVCFRLYAESDYDAFAPYPVPEIRRVALDSLVLQ ALSQRDPPHNNFFFFDGMKGNGIVECLGPK -------------------------------------------------------------- |
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Fusion Gene PPI Analysis for DHX34-SAE1 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for DHX34-SAE1 |
![]() (DrugBank Version 5.1.8 2021-05-08) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Related Diseases for DHX34-SAE1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | DHX34 | C4225275 | MENTAL RETARDATION, AUTOSOMAL DOMINANT 40 | 1 | GENOMICS_ENGLAND |