UTHEALTH HOME ABOUT SBMI A-Z WEBMAIL INSIDE THE UNIVERSITY |
![]() |
|||||||
|
Fusion Protein:DGCR8-DGCR14 |
Fusion Protein Summary |
![]() |
Fusion partner gene information | Fusion gene name: DGCR8-DGCR14 | FusionPDB ID: 22423 | FusionGDB2.0 ID: 22423 | Hgene | Tgene | Gene symbol | DGCR8 | DGCR14 | Gene ID | 54487 | 8220 |
Gene name | DGCR8 microprocessor complex subunit | ess-2 splicing factor homolog | |
Synonyms | C22orf12|DGCRK6|Gy1|pasha | DGCR13|DGCR14|DGS-H|DGS-I|DGSH|DGSI|ES2|ESS-2|Es2el|bis1 | |
Cytomap | 22q11.21 | 22q11.21|22q11.2 | |
Type of gene | protein-coding | protein-coding | |
Description | microprocessor complex subunit DGCR8DiGeorge syndrome critical region 8DiGeorge syndrome critical region gene 8 | splicing factor ESS-2 homologDiGeorge syndrome critical region gene 13DiGeorge syndrome critical region gene 14DiGeorge syndrome critical region gene DGSIDiGeorge syndrome gene HDiGeorge syndrome gene IProtein DGCR13diGeorge syndrome protein Hprot | |
Modification date | 20200320 | 20200320 | |
UniProtAcc | Q8WYQ5 | . | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000351989, ENST00000383024, ENST00000407755, | ENST00000252137, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 8 X 5 X 8=320 | 3 X 3 X 3=27 |
# samples | 9 | 3 | |
** MAII score | log2(9/320*10)=-1.83007499855769 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(3/27*10)=0.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: DGCR8 [Title/Abstract] AND DGCR14 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | DGCR8(20082318)-DGCR14(19127242), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | DGCR8-DGCR14 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. DGCR8-DGCR14 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. DGCR8-DGCR14 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. DGCR8-DGCR14 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 | DGCR8 | GO:0031053 | primary miRNA processing | 15531877|15574589|24449907|24910438 |
![]() * 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. |
![]() |
Top |
Fusion Gene Sample Information |
![]() |
![]() * 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 | COAD | TCGA-A6-5657-01A | DGCR8 | chr22 | 20082318 | - | DGCR14 | chr22 | 19127242 | - |
Top |
Fusion ORF Analysis |
![]() |
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) |
ENST00000351989 | DGCR8 | chr22 | 20082318 | - | ENST00000252137 | DGCR14 | chr22 | 19127242 | - | 6995 | 2217 | 429 | 3077 | 882 |
ENST00000383024 | DGCR8 | chr22 | 20082318 | - | ENST00000252137 | DGCR14 | chr22 | 19127242 | - | 6896 | 2118 | 429 | 2978 | 849 |
ENST00000407755 | DGCR8 | chr22 | 20082318 | - | ENST00000252137 | DGCR14 | chr22 | 19127242 | - | 6609 | 1831 | 142 | 2691 | 849 |
![]() |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000351989 | ENST00000252137 | DGCR8 | chr22 | 20082318 | - | DGCR14 | chr22 | 19127242 | - | 0.001855022 | 0.998145 |
ENST00000383024 | ENST00000252137 | DGCR8 | chr22 | 20082318 | - | DGCR14 | chr22 | 19127242 | - | 0.002152121 | 0.9978479 |
ENST00000407755 | ENST00000252137 | DGCR8 | chr22 | 20082318 | - | DGCR14 | chr22 | 19127242 | - | 0.002289099 | 0.99771094 |
Top |
Fusion Amino Acid Sequences |
![]() |
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >22423_22423_1_DGCR8-DGCR14_DGCR8_chr22_20082318_ENST00000351989_DGCR14_chr22_19127242_ENST00000252137_length(amino acids)=882AA_BP=594 METDESPSPLPCGPAGEAVMESRARPFQALPREQSPPPPLQTSSGAEVMDVGSGGDGQSELPAEDPFNFYGASLLSKGSFSKGRLLIDPN CSGHSPRTARHAPAVRKFSPDLKLLKDVKISVSFTESCRSKDRKVLYTGAERDVRAECGLLLSPVSGDVHACPFGGSVGDGVGIGGESAD KKDEENELDQEKRVEYAVLDELEDFTDNLELDEEGAGGFTAKAIVQRDRVDEEALNFPYEDDFDNDVDALLEEGLCAPKKRRTEEKYGGD SDHPSDGETSVQPMMTKIKTVLKSRGRPPTEPLPDGWIMTFHNSGVPVYLHRESRVVTWSRPYFLGTGSIRKHDPPLSSIPCLHYKKMKD NEEREQSSDLTPSGDVSPVKPLSRSAELEFPLDEPDSMGADPGPPDEKDPLGAEAAPGALGQVKAKVEVCKDESVDLEEFRSYLEKRFDF EQVTVKKFRTWAERRQFNREMKRKQAESERPILPANQKLITLSVQDAPTKKEFVINPNGKSEVCILHEYMQRVLKVRPVYNFFECENPSE PFGASVTIDGVTYGSGTASSKKLAKNKAARATLEILIPDFVKQTSEEKPKDSEELERQKDNLELPSAEHQAIESSQASVETWKYKAKNSL MYYPEGVPDEEQLFKKPRQVVHKNTRFLRDPFSQALSRCQLQQAAALNAQHKQGKVGPDGKELIPQESPRVGGFGFVATPSPAPGVNESP MMTWGEVENTPLRVEGSETPYVDRTPGPAFKILEPGRRERLGLKMANEAAAKNRAKKQEALRRVTENLASLTPKGLSPAMSPALQRLVSR -------------------------------------------------------------- >22423_22423_2_DGCR8-DGCR14_DGCR8_chr22_20082318_ENST00000383024_DGCR14_chr22_19127242_ENST00000252137_length(amino acids)=849AA_BP=561 METDESPSPLPCGPAGEAVMESRARPFQALPREQSPPPPLQTSSGAEVMDVGSGGDGQSELPAEDPFNFYGASLLSKGSFSKGRLLIDPN CSGHSPRTARHAPAVRKFSPDLKLLKDVKISVSFTESCRSKDRKVLYTGAERDVRAECGLLLSPVSGDVHACPFGGSVGDGVGIGGESAD KKDEENELDQEKRVEYAVLDELEDFTDNLELDEEGAGGFTAKAIVQRDRVDEEALNFPYEDDFDNDVDALLEEGLCAPKKRRTEEKYGGD SDHPSDGETSVQPMMTKIKTVLKSRGRPPTEPLPDGWIMTFHNSGVPVYLHRESRVVTWSRPYFLGTGSIRKHDPPLSSIPCLHYKKMKD NEEREQSSDLTPSGDVSPVKPLSRSAELEFPLDEPDSMGADPGPPDEKDPLGAEAAPGALGQVKAKVEVCKDESVDLEEFRSYLEKRFDF EQVTVKKFRTWAERRQFNREMKRKQAESERPILPANQKLITLSVQDAPTKKEFVINPNGKSEVCILHEYMQRVLKVRPVYNFFECARATL EILIPDFVKQTSEEKPKDSEELERQKDNLELPSAEHQAIESSQASVETWKYKAKNSLMYYPEGVPDEEQLFKKPRQVVHKNTRFLRDPFS QALSRCQLQQAAALNAQHKQGKVGPDGKELIPQESPRVGGFGFVATPSPAPGVNESPMMTWGEVENTPLRVEGSETPYVDRTPGPAFKIL EPGRRERLGLKMANEAAAKNRAKKQEALRRVTENLASLTPKGLSPAMSPALQRLVSRTASKYTDRALRASYTPSPARSTHLKTPASGLQT -------------------------------------------------------------- >22423_22423_3_DGCR8-DGCR14_DGCR8_chr22_20082318_ENST00000407755_DGCR14_chr22_19127242_ENST00000252137_length(amino acids)=849AA_BP=561 METDESPSPLPCGPAGEAVMESRARPFQALPREQSPPPPLQTSSGAEVMDVGSGGDGQSELPAEDPFNFYGASLLSKGSFSKGRLLIDPN CSGHSPRTARHAPAVRKFSPDLKLLKDVKISVSFTESCRSKDRKVLYTGAERDVRAECGLLLSPVSGDVHACPFGGSVGDGVGIGGESAD KKDEENELDQEKRVEYAVLDELEDFTDNLELDEEGAGGFTAKAIVQRDRVDEEALNFPYEDDFDNDVDALLEEGLCAPKKRRTEEKYGGD SDHPSDGETSVQPMMTKIKTVLKSRGRPPTEPLPDGWIMTFHNSGVPVYLHRESRVVTWSRPYFLGTGSIRKHDPPLSSIPCLHYKKMKD NEEREQSSDLTPSGDVSPVKPLSRSAELEFPLDEPDSMGADPGPPDEKDPLGAEAAPGALGQVKAKVEVCKDESVDLEEFRSYLEKRFDF EQVTVKKFRTWAERRQFNREMKRKQAESERPILPANQKLITLSVQDAPTKKEFVINPNGKSEVCILHEYMQRVLKVRPVYNFFECARATL EILIPDFVKQTSEEKPKDSEELERQKDNLELPSAEHQAIESSQASVETWKYKAKNSLMYYPEGVPDEEQLFKKPRQVVHKNTRFLRDPFS QALSRCQLQQAAALNAQHKQGKVGPDGKELIPQESPRVGGFGFVATPSPAPGVNESPMMTWGEVENTPLRVEGSETPYVDRTPGPAFKIL EPGRRERLGLKMANEAAAKNRAKKQEALRRVTENLASLTPKGLSPAMSPALQRLVSRTASKYTDRALRASYTPSPARSTHLKTPASGLQT -------------------------------------------------------------- |
Top |
Fusion Protein Functional Features |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr22:20082318/chr22:19127242) - 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 |
DGCR8 | . |
FUNCTION: Component of the microprocessor complex that acts as a RNA- and heme-binding protein that is involved in the initial step of microRNA (miRNA) biogenesis. Component of the microprocessor complex that is required to process primary miRNA transcripts (pri-miRNAs) to release precursor miRNA (pre-miRNA) in the nucleus. Within the microprocessor complex, DGCR8 function as a molecular anchor necessary for the recognition of pri-miRNA at dsRNA-ssRNA junction and directs DROSHA to cleave 11 bp away form the junction to release hairpin-shaped pre-miRNAs that are subsequently cut by the cytoplasmic DICER to generate mature miRNAs (PubMed:26027739, PubMed:26748718). The heme-bound DGCR8 dimer binds pri-miRNAs as a cooperative trimer (of dimers) and is active in triggering pri-miRNA cleavage, whereas the heme-free DGCR8 monomer binds pri-miRNAs as a dimer and is much less active. Both double-stranded and single-stranded regions of a pri-miRNA are required for its binding (PubMed:15531877, PubMed:15574589, PubMed:15589161, PubMed:16751099, PubMed:16906129, PubMed:16963499, PubMed:17159994). Specifically recognizes and binds N6-methyladenosine (m6A)-containing pri-miRNAs, a modification required for pri-miRNAs processing (PubMed:25799998). Involved in the silencing of embryonic stem cell self-renewal (By similarity). {ECO:0000250|UniProtKB:Q9EQM6, ECO:0000269|PubMed:15531877, ECO:0000269|PubMed:15574589, ECO:0000269|PubMed:15589161, ECO:0000269|PubMed:16751099, ECO:0000269|PubMed:16906129, ECO:0000269|PubMed:16963499, ECO:0000269|PubMed:17159994, ECO:0000269|PubMed:25799998, ECO:0000269|PubMed:26027739, ECO:0000269|PubMed:26748718}. | 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. |
![]() |
- 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 | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000351989 | - | 9 | 14 | 301_334 | 596.0 | 774.0 | Domain | WW |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000351989 | - | 9 | 14 | 511_578 | 596.0 | 774.0 | Domain | DRBM 1 |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000383024 | - | 8 | 13 | 301_334 | 563.0 | 741.0 | Domain | WW |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000407755 | - | 7 | 12 | 301_334 | 563.0 | 741.0 | Domain | WW |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000351989 | - | 9 | 14 | 1_275 | 596.0 | 774.0 | Region | Note=Necessary for nuclear localization and retention |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000383024 | - | 8 | 13 | 1_275 | 563.0 | 741.0 | Region | Note=Necessary for nuclear localization and retention |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000407755 | - | 7 | 12 | 1_275 | 563.0 | 741.0 | Region | Note=Necessary for nuclear localization and retention |
- 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 | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000351989 | - | 9 | 14 | 620_685 | 596.0 | 774.0 | Domain | DRBM 2 |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000383024 | - | 8 | 13 | 511_578 | 563.0 | 741.0 | Domain | DRBM 1 |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000383024 | - | 8 | 13 | 620_685 | 563.0 | 741.0 | Domain | DRBM 2 |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000407755 | - | 7 | 12 | 511_578 | 563.0 | 741.0 | Domain | DRBM 1 |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000407755 | - | 7 | 12 | 620_685 | 563.0 | 741.0 | Domain | DRBM 2 |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000351989 | - | 9 | 14 | 276_751 | 596.0 | 774.0 | Region | Note=Necessary for heme-binding and pri-miRNA processing |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000383024 | - | 8 | 13 | 276_751 | 563.0 | 741.0 | Region | Note=Necessary for heme-binding and pri-miRNA processing |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000407755 | - | 7 | 12 | 276_751 | 563.0 | 741.0 | Region | Note=Necessary for heme-binding and pri-miRNA processing |
Top |
Fusion Protein-Protein Interaction |
![]() |
![]() |
Gene | PPI interactors |
![]() |
Gene | STRING network |
DGCR8 | |
DGCR14 |
![]() |
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 |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000351989 | - | 9 | 14 | 701_773 | 596.0 | 774.0 | DROSHA |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000383024 | - | 8 | 13 | 701_773 | 563.0 | 741.0 | DROSHA |
Hgene | DGCR8 | chr22:20082318 | chr22:19127242 | ENST00000407755 | - | 7 | 12 | 701_773 | 563.0 | 741.0 | DROSHA |
Top |
Related Drugs to DGCR8-DGCR14 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
Top |
Related Diseases to DGCR8-DGCR14 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |