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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:DDB1-HEXA (FusionGDB2 ID:HG1642TG3073) |
Fusion Gene Summary for DDB1-HEXA |
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Fusion gene information | Fusion gene name: DDB1-HEXA | Fusion gene ID: hg1642tg3073 | Hgene | Tgene | Gene symbol | DDB1 | HEXA | Gene ID | 1642 | 3073 |
Gene name | damage specific DNA binding protein 1 | hexosaminidase subunit alpha | |
Synonyms | DDBA|UV-DDB1|XAP1|XPCE|XPE|XPE-BF | TSD | |
Cytomap | ('DDB1')('HEXA') 11q12.2 | 15q23 | |
Type of gene | protein-coding | protein-coding | |
Description | DNA damage-binding protein 1DDB p127 subunitDNA damage-binding protein aHBV X-associated protein 1UV-DDB 1UV-damaged DNA-binding factorUV-damaged DNA-binding protein 1XAP-1XPE-binding factordamage-specific DNA binding protein 1, 127kDaxeroderma | beta-hexosaminidase subunit alphaN-acetyl-beta-glucosaminidase subunit alphabeta-N-acetylhexosaminidase subunit alphahexosaminidase A (alpha polypeptide)hexosaminidase subunit A | |
Modification date | 20200327 | 20200315 | |
UniProtAcc | . | P06865 | |
Ensembl transtripts involved in fusion gene | ENST00000301764, ENST00000450997, ENST00000451943, ENST00000538470, ENST00000545930, | ||
Fusion gene scores | * DoF score | 12 X 17 X 6=1224 | 3 X 5 X 3=45 |
# samples | 16 | 5 | |
** MAII score | log2(16/1224*10)=-2.93545974780529 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(5/45*10)=0.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: DDB1 [Title/Abstract] AND HEXA [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | DDB1(61070101)-HEXA(72638618), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. |
* 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 |
Hgene | DDB1 | GO:0006511 | ubiquitin-dependent protein catabolic process | 11673459 |
Hgene | DDB1 | GO:0016567 | protein ubiquitination | 26431207|28886238 |
Hgene | DDB1 | GO:0035518 | histone H2A monoubiquitination | 22334663 |
Hgene | DDB1 | GO:0051702 | interaction with symbiont | 23137809 |
Hgene | DDB1 | GO:0070914 | UV-damage excision repair | 22334663 |
Tgene | HEXA | GO:0006024 | glycosaminoglycan biosynthetic process | 25645918 |
![]() * 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 |
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Fusion Gene ORF analysis for DDB1-HEXA |
![]() * 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 |
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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) |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
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Fusion Genomic Features for DDB1-HEXA |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
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Fusion Protein Features for DDB1-HEXA |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:61070101/:72638618) - 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 |
. | HEXA |
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: Hydrolyzes the non-reducing end N-acetyl-D-hexosamine and/or sulfated N-acetyl-D-hexosamine of glycoconjugates, such as the oligosaccharide moieties from proteins and neutral glycolipids, or from certain mucopolysaccharides (PubMed:11707436, PubMed:9694901, PubMed:8672428, PubMed:8123671). The isozyme S is as active as the isozyme A on the anionic bis-sulfated glycans, the chondroitin-6-sulfate trisaccharide (C6S-3), and the dermatan sulfate pentasaccharide, and the sulfated glycosphingolipid SM2 (PubMed:11707436). The isozyme B does not hydrolyze each of these substrates, however hydrolyzes efficiently neutral oligosaccharide (PubMed:11707436). Only the isozyme A is responsible for the degradation of GM2 gangliosides in the presence of GM2A (PubMed:9694901, PubMed:8672428, PubMed:8123671). {ECO:0000269|PubMed:11707436, ECO:0000269|PubMed:8123671, ECO:0000269|PubMed:8672428, ECO:0000269|PubMed:9694901}. |
![]() * 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 |
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Fusion Gene Sequence for DDB1-HEXA |
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Fusion Gene PPI Analysis for DDB1-HEXA |
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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 DDB1-HEXA |
![]() (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 DDB1-HEXA |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | DDB1 | C0019193 | Hepatitis, Toxic | 1 | CTD_human |
Hgene | DDB1 | C0024623 | Malignant neoplasm of stomach | 1 | CTD_human |
Hgene | DDB1 | C0038356 | Stomach Neoplasms | 1 | CTD_human |
Hgene | DDB1 | C0235874 | Disease Exacerbation | 1 | CTD_human |
Hgene | DDB1 | C0860207 | Drug-Induced Liver Disease | 1 | CTD_human |
Hgene | DDB1 | C1262760 | Hepatitis, Drug-Induced | 1 | CTD_human |
Hgene | DDB1 | C1708349 | Hereditary Diffuse Gastric Cancer | 1 | CTD_human |
Hgene | DDB1 | C3658290 | Drug-Induced Acute Liver Injury | 1 | CTD_human |
Hgene | DDB1 | C4277682 | Chemical and Drug Induced Liver Injury | 1 | CTD_human |
Hgene | DDB1 | C4279912 | Chemically-Induced Liver Toxicity | 1 | CTD_human |
Tgene | C0039373 | Tay-Sachs Disease | 31 | CTD_human;GENOMICS_ENGLAND;UNIPROT | |
Tgene | C0020796 | Profound Mental Retardation | 1 | CTD_human | |
Tgene | C0025363 | Mental Retardation, Psychosocial | 1 | CTD_human | |
Tgene | C0282220 | Amaurotic Familial Idiocy | 1 | CTD_human | |
Tgene | C0917816 | Mental deficiency | 1 | CTD_human | |
Tgene | C1848922 | Hexosaminidase alpha-Subunit Deficiency (Variant B) | 1 | CTD_human | |
Tgene | C3714756 | Intellectual Disability | 1 | CTD_human |