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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:MTCH1-C3 (FusionGDB2 ID:55228) |
Fusion Gene Summary for MTCH1-C3 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: MTCH1-C3 | Fusion gene ID: 55228 | Hgene | Tgene | Gene symbol | MTCH1 | C3 | Gene ID | 23787 | 718 |
| Gene name | mitochondrial carrier 1 | complement C3 | |
| Synonyms | CGI-64|PIG60|PSAP|SLC25A49 | AHUS5|ARMD9|ASP|C3a|C3b|CPAMD1|HEL-S-62p | |
| Cytomap | 6p21.2 | 19p13.3 | |
| Type of gene | protein-coding | protein-coding | |
| Description | mitochondrial carrier homolog 1cell proliferation-inducing protein 60presenilin-associated proteinsolute carrier family 25, member 49 | complement C3C3 and PZP-like alpha-2-macroglobulin domain-containing protein 1C3a anaphylatoxinacylation-stimulating protein cleavage productcomplement component 3complement component C3acomplement component C3bepididymis secretory sperm binding pr | |
| Modification date | 20200313 | 20200327 | |
| UniProtAcc | Q9NZJ7 | A6NLC5 | |
| Ensembl transtripts involved in fusion gene | ENST00000373627, ENST00000373616, ENST00000471737, ENST00000538808, | ENST00000245907, ENST00000599668, | |
| Fusion gene scores | * DoF score | 5 X 6 X 1=30 | 22 X 20 X 8=3520 |
| # samples | 6 | 22 | |
| ** MAII score | log2(6/30*10)=1 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(22/3520*10)=-4 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: MTCH1 [Title/Abstract] AND C3 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint | MTCH1(36949310)-C3(6684452), # 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) |
| 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 |
| Tgene | C3 | GO:0001934 | positive regulation of protein phosphorylation | 15833747 |
| Tgene | C3 | GO:0010575 | positive regulation of vascular endothelial growth factor production | 16452172 |
| Tgene | C3 | GO:0010828 | positive regulation of glucose transmembrane transport | 9059512|15833747 |
| Tgene | C3 | GO:0010866 | regulation of triglyceride biosynthetic process | 10432298 |
| Tgene | C3 | GO:0010884 | positive regulation of lipid storage | 9555951 |
| Tgene | C3 | GO:0045745 | positive regulation of G protein-coupled receptor signaling pathway | 15833747 |
| Fusion gene breakpoints across MTCH1 (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
| Fusion gene breakpoints across C3 (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
| 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 |
| ChiTaRS5.0 | N/A | AA169517 | MTCH1 | chr6 | 36949310 | - | C3 | chr19 | 6684452 | - |
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Fusion Gene ORF analysis for MTCH1-C3 |
| Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure. * 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 |
| intron-3CDS | ENST00000373627 | ENST00000245907 | MTCH1 | chr6 | 36949310 | - | C3 | chr19 | 6684452 | - |
| intron-intron | ENST00000373627 | ENST00000599668 | MTCH1 | chr6 | 36949310 | - | C3 | chr19 | 6684452 | - |
| intron-3CDS | ENST00000373616 | ENST00000245907 | MTCH1 | chr6 | 36949310 | - | C3 | chr19 | 6684452 | - |
| intron-intron | ENST00000373616 | ENST00000599668 | MTCH1 | chr6 | 36949310 | - | C3 | chr19 | 6684452 | - |
| intron-3CDS | ENST00000471737 | ENST00000245907 | MTCH1 | chr6 | 36949310 | - | C3 | chr19 | 6684452 | - |
| intron-intron | ENST00000471737 | ENST00000599668 | MTCH1 | chr6 | 36949310 | - | C3 | chr19 | 6684452 | - |
| intron-3CDS | ENST00000538808 | ENST00000245907 | MTCH1 | chr6 | 36949310 | - | C3 | chr19 | 6684452 | - |
| intron-intron | ENST00000538808 | ENST00000599668 | MTCH1 | chr6 | 36949310 | - | C3 | chr19 | 6684452 | - |
| ORFfinder result based on the fusion transcript sequence of in-frame fusion genes. |
| 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) |
| 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 |
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Fusion Genomic Features for MTCH1-C3 |
| FusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints. |
| Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
| Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page. |
| Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page. |
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Fusion Protein Features for MTCH1-C3 |
| Go to FGviewer for the breakpoints of :-: - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. |
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| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| MTCH1 | C3 |
| FUNCTION: Potential mitochondrial transporter. May play a role in apoptosis. {ECO:0000269|PubMed:12377771}. | FUNCTION: May play a role in neuronal and neurobehavioral development. {ECO:0000250|UniProtKB:Q1LY84}. |
| 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. |
| - 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 MTCH1-C3 |
| For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
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Fusion Gene PPI Analysis for MTCH1-C3 |
| 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 (BIOGRID-3.4.160) |
| Hgene | Hgene's interactors | Tgene | Tgene's interactors |
| - Retained PPIs in in-frame fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost PPIs in in-frame fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
| - Retained PPIs, but lost function due to frame-shift fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for MTCH1-C3 |
| Drugs targeting genes involved in this fusion gene. (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 MTCH1-C3 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Tgene | C3 | C3151071 | COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE | 5 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
| Tgene | C3 | C0242383 | Age related macular degeneration | 4 | CTD_human;GENOMICS_ENGLAND |
| Tgene | C3 | C2752037 | HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5 | 4 | GENOMICS_ENGLAND;UNIPROT |
| Tgene | C3 | C1969651 | Macular Degeneration, Age-Related, 9 | 2 | CTD_human;UNIPROT |
| Tgene | C3 | C0003257 | Antibody Deficiency Syndrome | 1 | CTD_human |
| Tgene | C3 | C0007787 | Transient Ischemic Attack | 1 | CTD_human |
| Tgene | C3 | C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | 1 | CTD_human |
| Tgene | C3 | C0013221 | Drug toxicity | 1 | CTD_human |
| Tgene | C3 | C0017665 | Membranous glomerulonephritis | 1 | CTD_human |
| Tgene | C3 | C0019061 | Hemolytic-Uremic Syndrome | 1 | GENOMICS_ENGLAND |
| Tgene | C3 | C0019193 | Hepatitis, Toxic | 1 | CTD_human |
| Tgene | C3 | C0021051 | Immunologic Deficiency Syndromes | 1 | CTD_human |
| Tgene | C3 | C0021655 | Insulin Resistance | 1 | CTD_human |
| Tgene | C3 | C0022660 | Kidney Failure, Acute | 1 | CTD_human |
| Tgene | C3 | C0030524 | Paratuberculosis | 1 | CTD_human |
| Tgene | C3 | C0030807 | Pemphigus | 1 | CTD_human |
| Tgene | C3 | C0030809 | Pemphigus Vulgaris | 1 | CTD_human |
| Tgene | C3 | C0034152 | Henoch-Schoenlein Purpura | 1 | CTD_human |
| Tgene | C3 | C0041755 | Adverse reaction to drug | 1 | CTD_human |
| Tgene | C3 | C0042386 | Vasculitis, Hemorrhagic | 1 | CTD_human |
| Tgene | C3 | C0086445 | Idiopathic Membranous Glomerulonephritis | 1 | CTD_human |
| Tgene | C3 | C0086922 | Rheumatoid Purpura | 1 | CTD_human |
| Tgene | C3 | C0238281 | Middle Cerebral Artery Syndrome | 1 | CTD_human |
| Tgene | C3 | C0242461 | Purpura, Nonthrombocytopenic | 1 | CTD_human |
| Tgene | C3 | C0263313 | Pemphigus Foliaceus | 1 | CTD_human |
| Tgene | C3 | C0272242 | Complement deficiency disease | 1 | GENOMICS_ENGLAND |
| Tgene | C3 | C0376362 | Purpura Hemorrhagica | 1 | CTD_human |
| Tgene | C3 | C0472381 | Posterior Circulation Transient Ischemic Attack | 1 | CTD_human |
| Tgene | C3 | C0740376 | Middle Cerebral Artery Thrombosis | 1 | CTD_human |
| Tgene | C3 | C0740391 | Middle Cerebral Artery Occlusion | 1 | CTD_human |
| Tgene | C3 | C0740392 | Infarction, Middle Cerebral Artery | 1 | CTD_human |
| Tgene | C3 | C0751019 | Carotid Circulation Transient Ischemic Attack | 1 | CTD_human |
| Tgene | C3 | C0751020 | Transient Ischemic Attack, Vertebrobasilar Circulation | 1 | CTD_human |
| Tgene | C3 | C0751021 | Crescendo Transient Ischemic Attacks | 1 | CTD_human |
| Tgene | C3 | C0751022 | Brain Stem Ischemia, Transient | 1 | CTD_human |
| Tgene | C3 | C0751845 | Middle Cerebral Artery Embolus | 1 | CTD_human |
| Tgene | C3 | C0751846 | Left Middle Cerebral Artery Infarction | 1 | CTD_human |
| Tgene | C3 | C0751847 | Embolic Infarction, Middle Cerebral Artery | 1 | CTD_human |
| Tgene | C3 | C0751848 | Thrombotic Infarction, Middle Cerebral Artery | 1 | CTD_human |
| Tgene | C3 | C0751849 | Right Middle Cerebral Artery Infarction | 1 | CTD_human |
| Tgene | C3 | C0860207 | Drug-Induced Liver Disease | 1 | CTD_human |
| Tgene | C3 | C0917805 | Transient Cerebral Ischemia | 1 | CTD_human |
| Tgene | C3 | C0920563 | Insulin Sensitivity | 1 | CTD_human |
| Tgene | C3 | C1262760 | Hepatitis, Drug-Induced | 1 | CTD_human |
| Tgene | C3 | C1332655 | Complement component 3 deficiency | 1 | GENOMICS_ENGLAND |
| Tgene | C3 | C1527335 | Transient Ischemic Attack, Anterior Circulation | 1 | CTD_human |
| Tgene | C3 | C1565662 | Acute Kidney Insufficiency | 1 | CTD_human |
| Tgene | C3 | C1704378 | Heymann Nephritis | 1 | CTD_human |
| Tgene | C3 | C2609414 | Acute kidney injury | 1 | CTD_human |
| Tgene | C3 | C2931788 | Atypical Hemolytic Uremic Syndrome | 1 | CTD_human;GENOMICS_ENGLAND |
| Tgene | C3 | C3658290 | Drug-Induced Acute Liver Injury | 1 | CTD_human |
| Tgene | C3 | C4087273 | C3 glomerulopathy | 1 | GENOMICS_ENGLAND |
| Tgene | C3 | C4277682 | Chemical and Drug Induced Liver Injury | 1 | CTD_human |
| Tgene | C3 | C4279912 | Chemically-Induced Liver Toxicity | 1 | CTD_human |
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