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Fusion Protein:CEACAM5-AP1G1 |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: CEACAM5-AP1G1 | FusionPDB ID: 15505 | FusionGDB2.0 ID: 15505 | Hgene | Tgene | Gene symbol | CEACAM5 | AP1G1 | Gene ID | 1048 | 164 |
| Gene name | CEA cell adhesion molecule 5 | adaptor related protein complex 1 subunit gamma 1 | |
| Synonyms | CD66e|CEA | ADTG|CLAPG1 | |
| Cytomap | 19q13.2 | 16q22.2 | |
| Type of gene | protein-coding | protein-coding | |
| Description | carcinoembryonic antigen-related cell adhesion molecule 5carcinoembryonic antigen related cell adhesion molecule 5meconium antigen 100 | AP-1 complex subunit gamma-1adapter-related protein complex 1 subunit gamma-1adaptor protein complex AP-1 subunit gamma-1adaptor related protein complex 1 gamma 1 subunitclathrin assembly protein complex 1 gamma large chainclathrin assembly protein c | |
| Modification date | 20200313 | 20200313 | |
| UniProtAcc | P06731 | O43747 | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000221992, ENST00000398599, ENST00000405816, | ENST00000564155, ENST00000570297, ENST00000299980, ENST00000393512, ENST00000423132, ENST00000433195, ENST00000569748, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 10 X 11 X 4=440 | 12 X 12 X 5=720 |
| # samples | 10 | 14 | |
| ** MAII score | log2(10/440*10)=-2.13750352374993 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(14/720*10)=-2.36257007938471 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context (manual curation of fusion genes in FusionPDB) | PubMed: CEACAM5 [Title/Abstract] AND AP1G1 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | CEACAM5(42224127)-AP1G1(71767062), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | CEACAM5-AP1G1 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. CEACAM5-AP1G1 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. CEACAM5-AP1G1 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. CEACAM5-AP1G1 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. CEACAM5-AP1G1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target 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) |
| Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Partner | Gene | GO ID | GO term | PubMed ID |
| Hgene | CEACAM5 | GO:0010832 | negative regulation of myotube differentiation | 8408226|10931872 |
| Hgene | CEACAM5 | GO:0034109 | homotypic cell-cell adhesion | 10864933 |
| Hgene | CEACAM5 | GO:0043066 | negative regulation of apoptotic process | 11448920 |
| Hgene | CEACAM5 | GO:2000811 | negative regulation of anoikis | 10910050 |
| Fusion gene breakpoints across CEACAM5 (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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| Fusion gene breakpoints across AP1G1 (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
| Fusion gene information from FusionGDB2.0. |
| Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0) * 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 | STAD | TCGA-BR-8683-01A | CEACAM5 | chr19 | 42224127 | + | AP1G1 | chr16 | 71767062 | - |
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Fusion ORF Analysis |
| Fusion information from ORFfinder translation from full-length transcript sequence from FusionPDB. |
| 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) |
| ENST00000398599 | CEACAM5 | chr19 | 42224127 | + | ENST00000569748 | AP1G1 | chr16 | 71767062 | - | 3192 | 1915 | 81 | 1949 | 622 |
| ENST00000221992 | CEACAM5 | chr19 | 42224127 | + | ENST00000569748 | AP1G1 | chr16 | 71767062 | - | 3162 | 1885 | 48 | 1919 | 623 |
| ENST00000405816 | CEACAM5 | chr19 | 42224127 | + | ENST00000569748 | AP1G1 | chr16 | 71767062 | - | 3131 | 1854 | 17 | 1888 | 623 |
| DeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated. |
| Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
| ENST00000398599 | ENST00000569748 | CEACAM5 | chr19 | 42224127 | + | AP1G1 | chr16 | 71767062 | - | 0.002155877 | 0.9978441 |
| ENST00000221992 | ENST00000569748 | CEACAM5 | chr19 | 42224127 | + | AP1G1 | chr16 | 71767062 | - | 0.002354644 | 0.9976453 |
| ENST00000405816 | ENST00000569748 | CEACAM5 | chr19 | 42224127 | + | AP1G1 | chr16 | 71767062 | - | 0.00221644 | 0.9977836 |
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Fusion Amino Acid Sequences |
| For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
| >FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >15505_15505_1_CEACAM5-AP1G1_CEACAM5_chr19_42224127_ENST00000221992_AP1G1_chr16_71767062_ENST00000569748_length(amino acids)=623AA_BP= MTKRSWNSSSSPQRRTEQTAETMESPSAPPHRWCIPWQRLLLTASLLTFWNPPTTAKLTIESTPFNVAEGKEVLLLVHNLPQHLFGYSWY KGERVDGNRQIIGYVIGTQQATPGPAYSGREIIYPNASLLIQNIIQNDTGFYTLHVIKSDLVNEEATGQFRVYPELPKPSISSNNSKPVE DKDAVAFTCEPETQDATYLWWVNNQSLPVSPRLQLSNGNRTLTLFNVTRNDTASYKCETQNPVSARRSDSVILNVLYGPDAPTISPLNTS YRSGENLNLSCHAASNPPAQYSWFVNGTFQQSTQELFIPNITVNNSGSYTCQAHNSDTGLNRTTVTTITVYAEPPKPFITSNNSNPVEDE DAVALTCEPEIQNTTYLWWVNNQSLPVSPRLQLSNDNRTLTLLSVTRNDVGPYECGIQNKLSVDHSDPVILNVLYGPDDPTISPSYTYYR PGVNLSLSCHAASNPPAQYSWLIDGNIQQHTQELFISNITEKNSGLYTCQANNSASGHSRTTVKTITVSAELPKPSISSNNSKPVEDKDA -------------------------------------------------------------- >15505_15505_2_CEACAM5-AP1G1_CEACAM5_chr19_42224127_ENST00000398599_AP1G1_chr16_71767062_ENST00000569748_length(amino acids)=622AA_BP= MTKRSWNSSSSPQRRTEQTAETMESPSAPPHRWCIPWQRLLLTASLLTFWNPPTTAKLTIESTPFNVAEGKEVLLLVHNLPQHLFGYSWY KGERVDGNRQIIGYVIGTQQATPGPAYSGREIIYPNASLLIQNIIQNDTGFYTLHVIKSDLVNEEATGQFRVYPELPKPSISSNNSKPVE DKDAVAFTCEPETQDATYLWWVNNQSLPVSPRLQLSNGNRTLTLFNVTRNDTASYKCETQNPVSARRSDSVILNVLYGPDAPTISPLNTS YRSGENLNLSCHAASNPPAQYSWFVNGTFQQSTQELFIPNITVNNSGSYTCQAHNSDTGLNRTTVTTITVYEPPKPFITSNNSNPVEDED AVALTCEPEIQNTTYLWWVNNQSLPVSPRLQLSNDNRTLTLLSVTRNDVGPYECGIQNKLSVDHSDPVILNVLYGPDDPTISPSYTYYRP GVNLSLSCHAASNPPAQYSWLIDGNIQQHTQELFISNITEKNSGLYTCQANNSASGHSRTTVKTITVSAELPKPSISSNNSKPVEDKDAV -------------------------------------------------------------- >15505_15505_3_CEACAM5-AP1G1_CEACAM5_chr19_42224127_ENST00000405816_AP1G1_chr16_71767062_ENST00000569748_length(amino acids)=623AA_BP= MTKRSWNSSSSPQRRTEQTAETMESPSAPPHRWCIPWQRLLLTASLLTFWNPPTTAKLTIESTPFNVAEGKEVLLLVHNLPQHLFGYSWY KGERVDGNRQIIGYVIGTQQATPGPAYSGREIIYPNASLLIQNIIQNDTGFYTLHVIKSDLVNEEATGQFRVYPELPKPSISSNNSKPVE DKDAVAFTCEPETQDATYLWWVNNQSLPVSPRLQLSNGNRTLTLFNVTRNDTASYKCETQNPVSARRSDSVILNVLYGPDAPTISPLNTS YRSGENLNLSCHAASNPPAQYSWFVNGTFQQSTQELFIPNITVNNSGSYTCQAHNSDTGLNRTTVTTITVYAEPPKPFITSNNSNPVEDE DAVALTCEPEIQNTTYLWWVNNQSLPVSPRLQLSNDNRTLTLLSVTRNDVGPYECGIQNKLSVDHSDPVILNVLYGPDDPTISPSYTYYR PGVNLSLSCHAASNPPAQYSWLIDGNIQQHTQELFISNITEKNSGLYTCQANNSASGHSRTTVKTITVSAELPKPSISSNNSKPVEDKDA -------------------------------------------------------------- |
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Fusion Protein Functional Features |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr19:42224127/chr16:71767062) - 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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| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| CEACAM5 | AP1G1 |
| FUNCTION: Cell surface glycoprotein that plays a role in cell adhesion, intracellular signaling and tumor progression (PubMed:2803308, PubMed:10910050, PubMed:10864933). Mediates homophilic and heterophilic cell adhesion with other carcinoembryonic antigen-related cell adhesion molecules, such as CEACAM6 (PubMed:2803308). Plays a role as an oncogene by promoting tumor progression; induces resistance to anoikis of colorectal carcinoma cells (PubMed:10910050). {ECO:0000269|PubMed:10864933, ECO:0000269|PubMed:10910050, ECO:0000269|PubMed:2803308}.; FUNCTION: (Microbial infection) Receptor for E.coli Dr adhesins. Binding of E.coli Dr adhesins leads to dissociation of the homodimer. {ECO:0000269|PubMed:18086185}. | FUNCTION: Subunit of clathrin-associated adaptor protein complex 1 that plays a role in protein sorting in the late-Golgi/trans-Golgi network (TGN) and/or endosomes. The AP complexes mediate both the recruitment of clathrin to membranes and the recognition of sorting signals within the cytosolic tails of transmembrane cargo molecules. In association with AFTPH/aftiphilin in the aftiphilin/p200/gamma-synergin complex, involved in the trafficking of transferrin from early to recycling endosomes, and the membrane trafficking of furin and the lysosomal enzyme cathepsin D between the trans-Golgi network (TGN) and endosomes (PubMed:15758025). {ECO:0000269|PubMed:15758025}. |
| Retention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at * Minus value of BPloci means that the break pointn is located before the CDS. |
| - 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 | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000221992 | + | 7 | 10 | 145_232 | 590.3333333333334 | 848.6666666666666 | Domain | Ig-like C2-type 1 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000221992 | + | 7 | 10 | 240_315 | 590.3333333333334 | 848.6666666666666 | Domain | Ig-like C2-type 2 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000221992 | + | 7 | 10 | 323_410 | 590.3333333333334 | 848.6666666666666 | Domain | Ig-like C2-type 3 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000221992 | + | 7 | 10 | 35_144 | 590.3333333333334 | 848.6666666666666 | Domain | Ig-like V-type |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000221992 | + | 7 | 10 | 418_495 | 590.3333333333334 | 848.6666666666666 | Domain | Ig-like C2-type 4 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000221992 | + | 7 | 10 | 501_588 | 590.3333333333334 | 848.6666666666666 | Domain | Ig-like C2-type 5 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000398599 | + | 7 | 10 | 145_232 | 589.3333333333334 | 685.6666666666666 | Domain | Ig-like C2-type 1 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000398599 | + | 7 | 10 | 240_315 | 589.3333333333334 | 685.6666666666666 | Domain | Ig-like C2-type 2 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000398599 | + | 7 | 10 | 323_410 | 589.3333333333334 | 685.6666666666666 | Domain | Ig-like C2-type 3 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000398599 | + | 7 | 10 | 35_144 | 589.3333333333334 | 685.6666666666666 | Domain | Ig-like V-type |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000398599 | + | 7 | 10 | 418_495 | 589.3333333333334 | 685.6666666666666 | Domain | Ig-like C2-type 4 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000398599 | + | 7 | 10 | 501_588 | 589.3333333333334 | 685.6666666666666 | Domain | Ig-like C2-type 5 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000405816 | + | 7 | 10 | 145_232 | 590.3333333333334 | 696.0 | Domain | Ig-like C2-type 1 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000405816 | + | 7 | 10 | 240_315 | 590.3333333333334 | 696.0 | Domain | Ig-like C2-type 2 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000405816 | + | 7 | 10 | 323_410 | 590.3333333333334 | 696.0 | Domain | Ig-like C2-type 3 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000405816 | + | 7 | 10 | 35_144 | 590.3333333333334 | 696.0 | Domain | Ig-like V-type |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000405816 | + | 7 | 10 | 418_495 | 590.3333333333334 | 696.0 | Domain | Ig-like C2-type 4 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000405816 | + | 7 | 10 | 501_588 | 590.3333333333334 | 696.0 | Domain | Ig-like C2-type 5 |
| - 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 | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000221992 | + | 7 | 10 | 593_675 | 590.3333333333334 | 848.6666666666666 | Domain | Ig-like C2-type 6 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000398599 | + | 7 | 10 | 593_675 | 589.3333333333334 | 685.6666666666666 | Domain | Ig-like C2-type 6 |
| Hgene | CEACAM5 | chr19:42224127 | chr16:71767062 | ENST00000405816 | + | 7 | 10 | 593_675 | 590.3333333333334 | 696.0 | Domain | Ig-like C2-type 6 |
| Tgene | AP1G1 | chr19:42224127 | chr16:71767062 | ENST00000299980 | 21 | 23 | 702_817 | 789.0 | 823.0 | Domain | GAE | |
| Tgene | AP1G1 | chr19:42224127 | chr16:71767062 | ENST00000393512 | 22 | 24 | 702_817 | 792.0 | 826.0 | Domain | GAE | |
| Tgene | AP1G1 | chr19:42224127 | chr16:71767062 | ENST00000569748 | 24 | 26 | 702_817 | 789.0 | 823.0 | Domain | GAE |
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Fusion Protein-Protein Interaction |
| Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in |
| Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160) |
| Gene | PPI interactors |
| Protein-protein interactors based on sequence similarity (STRING) |
| Gene | STRING network |
| CEACAM5 | |
| AP1G1 |
| - Retained interactions in fusion protein (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost interactions due to fusion (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs to CEACAM5-AP1G1 |
| Drugs used for this fusion-positive patient. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to CEACAM5-AP1G1 |
| Diseases that have this fusion gene. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Disease | Source | PMID |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
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