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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:ALG14-C1orf194 (FusionGDB2 ID:HG199857TG127003) |
Fusion Gene Summary for ALG14-C1orf194 |
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Fusion gene information | Fusion gene name: ALG14-C1orf194 | Fusion gene ID: hg199857tg127003 | Hgene | Tgene | Gene symbol | ALG14 | C1orf194 | Gene ID | 199857 | 127003 |
Gene name | ALG14 UDP-N-acetylglucosaminyltransferase subunit | chromosome 1 open reading frame 194 | |
Synonyms | CMS15 | - | |
Cytomap | ('ALG14')('C1orf194') 1p21.3 | 1p13.3 | |
Type of gene | protein-coding | protein-coding | |
Description | UDP-N-acetylglucosamine transferase subunit ALG14 homolog | protein C1orf194uncharacterized protein C1orf194 | |
Modification date | 20200313 | 20200313 | |
UniProtAcc | Q96F25 | Q5T5A4 | |
Ensembl transtripts involved in fusion gene | ENST00000370205, ENST00000495856, | ||
Fusion gene scores | * DoF score | 8 X 5 X 5=200 | 3 X 1 X 3=9 |
# samples | 8 | 4 | |
** MAII score | log2(8/200*10)=-1.32192809488736 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(4/9*10)=2.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: ALG14 [Title/Abstract] AND C1orf194 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | ALG14(95492685)-C1orf194(109649281), # samples:3 | ||
Anticipated loss of major functional domain due to fusion event. | ALG14-C1orf194 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF. ALG14-C1orf194 seems lost the major protein functional domain in Hgene 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 |
![]() * 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 | BRCA | TCGA-BH-A1FC-01A | ALG14 | chr1 | 95492685 | - | C1orf194 | chr1 | 109649281 | - |
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Fusion Gene ORF analysis for ALG14-C1orf194 |
![]() * 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 |
Frame-shift | ENST00000370205 | ENST00000369945 | ALG14 | chr1 | 95492685 | - | C1orf194 | chr1 | 109649281 | - |
Frame-shift | ENST00000370205 | ENST00000369948 | ALG14 | chr1 | 95492685 | - | C1orf194 | chr1 | 109649281 | - |
Frame-shift | ENST00000370205 | ENST00000369949 | ALG14 | chr1 | 95492685 | - | C1orf194 | chr1 | 109649281 | - |
intron-3CDS | ENST00000495856 | ENST00000369945 | ALG14 | chr1 | 95492685 | - | C1orf194 | chr1 | 109649281 | - |
intron-3CDS | ENST00000495856 | ENST00000369948 | ALG14 | chr1 | 95492685 | - | C1orf194 | chr1 | 109649281 | - |
intron-3CDS | ENST00000495856 | ENST00000369949 | ALG14 | chr1 | 95492685 | - | C1orf194 | chr1 | 109649281 | - |
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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 ALG14-C1orf194 |
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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 ALG14-C1orf194 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:95492685/:109649281) - 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 |
ALG14 | C1orf194 |
FUNCTION: May be involved in protein N-glycosylation. May play a role in the second step of the dolichol-linked oligosaccharide pathway. May anchor the catalytic subunit ALG13 to the ER. {ECO:0000269|PubMed:16100110}. | FUNCTION: May play an important role for the maintenance of myelin-axon integrity (By similarity). May affect intracellular Ca(2+) homeostasis (PubMed:31199454). {ECO:0000250|UniProtKB:Q9DAD0, ECO:0000269|PubMed:31199454}. |
![]() * 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 ALG14-C1orf194 |
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Fusion Gene PPI Analysis for ALG14-C1orf194 |
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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 ALG14-C1orf194 |
![]() (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 ALG14-C1orf194 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ALG14 | C4015596 | MYASTHENIC SYNDROME, CONGENITAL, 15 | 3 | GENOMICS_ENGLAND;UNIPROT |
Hgene | ALG14 | C0751882 | Myasthenic Syndromes, Congenital | 1 | CTD_human;GENOMICS_ENGLAND |
Hgene | ALG14 | C3714756 | Intellectual Disability | 1 | GENOMICS_ENGLAND |