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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:AHCY-RPLP1 (FusionGDB2 ID:HG191TG6176) |
Fusion Gene Summary for AHCY-RPLP1 |
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Fusion gene information | Fusion gene name: AHCY-RPLP1 | Fusion gene ID: hg191tg6176 | Hgene | Tgene | Gene symbol | AHCY | RPLP1 | Gene ID | 191 | 6176 |
Gene name | adenosylhomocysteinase | ribosomal protein lateral stalk subunit P1 | |
Synonyms | SAHH|adoHcyase | LP1|P1|RPP1 | |
Cytomap | ('AHCY')('RPLP1') 20q11.22 | 15q23 | |
Type of gene | protein-coding | protein-coding | |
Description | adenosylhomocysteinaseS-adenosyl-L-homocysteine hydrolaseS-adenosylhomocysteine hydrolaseepididymis secretory sperm binding protein | 60S acidic ribosomal protein P1acidic ribosomal phosphoprotein P1large ribosomal subunit protein P1ribosomal protein, large, P1 | |
Modification date | 20200320 | 20200313 | |
UniProtAcc | . | . | |
Ensembl transtripts involved in fusion gene | ENST00000217426, ENST00000538132, ENST00000468908, | ||
Fusion gene scores | * DoF score | 9 X 9 X 4=324 | 19 X 14 X 8=2128 |
# samples | 9 | 21 | |
** MAII score | log2(9/324*10)=-1.84799690655495 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(21/2128*10)=-3.34103691783507 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: AHCY [Title/Abstract] AND RPLP1 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | AHCY(32883201)-RPLP1(69745986), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | AHCY-RPLP1 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF. AHCY-RPLP1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. AHCY-RPLP1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF. AHCY-RPLP1 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism 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 |
![]() * 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 | COAD | TCGA-A6-6648-01A | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + |
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Fusion Gene ORF analysis for AHCY-RPLP1 |
![]() * 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-intron | ENST00000217426 | ENST00000357790 | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + |
5CDS-intron | ENST00000217426 | ENST00000560274 | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + |
5CDS-intron | ENST00000538132 | ENST00000357790 | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + |
5CDS-intron | ENST00000538132 | ENST00000560274 | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + |
5UTR-3CDS | ENST00000468908 | ENST00000260379 | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + |
5UTR-intron | ENST00000468908 | ENST00000357790 | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + |
5UTR-intron | ENST00000468908 | ENST00000560274 | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + |
Frame-shift | ENST00000538132 | ENST00000260379 | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + |
In-frame | ENST00000217426 | ENST00000260379 | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + |
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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) |
ENST00000217426 | AHCY | chr20 | 32883201 | - | ENST00000260379 | RPLP1 | chr15 | 69745986 | + | 979 | 297 | 78 | 569 | 163 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000217426 | ENST00000260379 | AHCY | chr20 | 32883201 | - | RPLP1 | chr15 | 69745986 | + | 0.001617414 | 0.99838257 |
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Fusion Genomic Features for AHCY-RPLP1 |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
AHCY | chr20 | 32883200 | - | RPLP1 | chr15 | 69745985 | + | 5.15E-07 | 0.9999995 |
AHCY | chr20 | 32883200 | - | RPLP1 | chr15 | 69745985 | + | 5.15E-07 | 0.9999995 |
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Fusion Protein Features for AHCY-RPLP1 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr20:32883201/chr15:69745986) - 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 |
- 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 | AHCY | chr20:32883201 | chr15:69745986 | ENST00000217426 | - | 2 | 10 | 157_159 | 73 | 433.0 | Nucleotide binding | NAD |
Hgene | AHCY | chr20:32883201 | chr15:69745986 | ENST00000217426 | - | 2 | 10 | 222_227 | 73 | 433.0 | Nucleotide binding | NAD |
Hgene | AHCY | chr20:32883201 | chr15:69745986 | ENST00000217426 | - | 2 | 10 | 299_301 | 73 | 433.0 | Nucleotide binding | NAD |
Hgene | AHCY | chr20:32883201 | chr15:69745986 | ENST00000538132 | - | 2 | 10 | 157_159 | 45 | 405.0 | Nucleotide binding | NAD |
Hgene | AHCY | chr20:32883201 | chr15:69745986 | ENST00000538132 | - | 2 | 10 | 222_227 | 45 | 405.0 | Nucleotide binding | NAD |
Hgene | AHCY | chr20:32883201 | chr15:69745986 | ENST00000538132 | - | 2 | 10 | 299_301 | 45 | 405.0 | Nucleotide binding | NAD |
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Fusion Gene Sequence for AHCY-RPLP1 |
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>3072_3072_1_AHCY-RPLP1_AHCY_chr20_32883201_ENST00000217426_RPLP1_chr15_69745986_ENST00000260379_length(transcript)=979nt_BP=297nt CGGCGCTGCCCGCCCAGTTCCTGTTCCCAGACTGAGGCCCAGCCCCCTTCGCCCGTTTCCATCACGAGTGCCGCCAGCATGTCTGACAAA CTGCCCTACAAAGTCGCCGACATCGGCCTGGCTGCCTGGGGACGCAAGGCCCTGGACATTGCTGAGAACGAGATGCCGGGCCTGATGCGT ATGCGGGAGCGGTACTCGGCCTCCAAGCCACTGAAGGGCGCCCGCATCGCTGGCTGCCTGCACATGACCGTGGAGACGGCCGTCCTCATT GAGACCCTCGTCACCCTGGGTGCTGAGGAGGATAAGATCAATGCCCTCATTAAAGCAGCCGGTGTAAATGTTGAGCCTTTTTGGCCTGGC TTGTTTGCAAAGGCCCTGGCCAACGTCAACATTGGGAGCCTCATCTGCAATGTAGGGGCCGGTGGACCTGCTCCAGCAGCTGGTGCTGCA CCAGCAGGAGGTCCTGCCCCCTCCACTGCTGCTGCTCCAGCTGAGGAGAAGAAAGTGGAAGCAAAGAAAGAAGAATCCGAGGAGTCTGAT GATGACATGGGCTTTGGTCTTTTTGACTAAACCTCTTTTATAACATGTTCAATAAAAAGCTGAACTTTACTGCTGTTGGTCTTGTCCATA GTTTTGGAATGTGCTCTGCAAAAATGGTCTGTTTTGTAATGTTGGCTTTCAGCCTATTCTGCCATGACACAGGCTGGATTTTCCCTGCCA CCATTGCCGGATGTGAGATTTAGACAATCCTGATGCTAACAAGAAGGCACCTCATGGTACAGTGTTGAAAACTGCACTGGGGTGGCAGGA GGAAGGATCAGAGCAGATGCTTTGTCCAGGTTACCTGTGTAAACTTGATGATTATAAGGTGTGTCCCCTACACTGGGGGTGGAGGGTAAT >3072_3072_1_AHCY-RPLP1_AHCY_chr20_32883201_ENST00000217426_RPLP1_chr15_69745986_ENST00000260379_length(amino acids)=163AA_BP=73 MSDKLPYKVADIGLAAWGRKALDIAENEMPGLMRMRERYSASKPLKGARIAGCLHMTVETAVLIETLVTLGAEEDKINALIKAAGVNVEP -------------------------------------------------------------- |
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Fusion Gene PPI Analysis for AHCY-RPLP1 |
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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 AHCY-RPLP1 |
![]() (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 AHCY-RPLP1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | AHCY | C3151058 | S-adenosylhomocysteine hydrolase deficiency | 13 | CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Hgene | AHCY | C4510276 | Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | 10 | CLINGEN |
Hgene | AHCY | C0002514 | Amino Acid Metabolism, Inborn Errors | 1 | CTD_human |
Hgene | AHCY | C0003129 | Anoxemia | 1 | CTD_human |
Hgene | AHCY | C0003130 | Anoxia | 1 | CTD_human |
Hgene | AHCY | C0019202 | Hepatolenticular Degeneration | 1 | CTD_human |
Hgene | AHCY | C0152013 | Adenocarcinoma of lung (disorder) | 1 | CTD_human |
Hgene | AHCY | C0242184 | Hypoxia | 1 | CTD_human |
Hgene | AHCY | C0268621 | Hepatic methionine adenosyltransferase deficiency | 1 | CTD_human |
Hgene | AHCY | C0400966 | Non-alcoholic Fatty Liver Disease | 1 | CTD_human |
Hgene | AHCY | C0700292 | Hypoxemia | 1 | CTD_human |
Hgene | AHCY | C0750905 | Amino Acid Metabolism, Inherited Disorders | 1 | CTD_human |
Hgene | AHCY | C1527352 | Hepatic Form of Wilson Disease | 1 | CTD_human |
Hgene | AHCY | C1847720 | Hypermethioninemia due to deficiency of glycine N-methyltransferase | 1 | CTD_human |
Hgene | AHCY | C3241937 | Nonalcoholic Steatohepatitis | 1 | CTD_human |
Hgene | AHCY | C4048705 | Hypermethioninemia | 1 | CTD_human |