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Fusion Protein:KMT2C-GTF2IRD1 |
Fusion Gene and Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: KMT2C-GTF2IRD1 | FusionPDB ID: 43248 | FusionGDB2.0 ID: 54207 | Hgene | Tgene | Gene symbol | KMT2C | GTF2IRD1 | Gene ID | 58508 | 9569 |
| Gene name | lysine methyltransferase 2C | GTF2I repeat domain containing 1 | |
| Synonyms | HALR|KLEFS2|MLL3 | BEN|CREAM1|GTF3|MUSTRD1|RBAP2|WBS|WBSCR11|WBSCR12|hMusTRD1alpha1 | |
| Cytomap | 7q36.1 | 7q11.23 | |
| Type of gene | protein-coding | protein-coding | |
| Description | histone-lysine N-methyltransferase 2CALR-like proteinhistone-lysine N-methyltransferase MLL3histone-lysine N-methyltransferase, H3 lysine-4 specifichomologous to ALR proteinlysine (K)-specific methyltransferase 2Cmyeloid/lymphoid or mixed-lineage le | general transcription factor II-I repeat domain-containing protein 1USE B1-binding proteinWilliams-Beuren syndrome chromosome region 11binding factor for early enhancergeneral transcription factor 3general transcription factor IIImuscle TFII-I repea | |
| Modification date | 20200320 | 20200313 | |
| UniProtAcc | Q8NEZ4 Main function of 5'-partner protein: FUNCTION: Histone methyltransferase that methylates 'Lys-4' of histone H3 (PubMed:22266653). H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation. Central component of the MLL2/3 complex, a coactivator complex of nuclear receptors, involved in transcriptional coactivation. KMT2C/MLL3 may be a catalytic subunit of this complex. May be involved in leukemogenesis and developmental disorder. {ECO:0000269|PubMed:17500065, ECO:0000269|PubMed:22266653}. | Q9UHL9 Main function of 5'-partner protein: FUNCTION: May be a transcription regulator involved in cell-cycle progression and skeletal muscle differentiation. May repress GTF2I transcriptional functions, by preventing its nuclear residency, or by inhibiting its transcriptional activation. May contribute to slow-twitch fiber type specificity during myogenesis and in regenerating muscles. Binds troponin I slow-muscle fiber enhancer (USE B1). Binds specifically and with high affinity to the EFG sequences derived from the early enhancer of HOXC8 (By similarity). {ECO:0000250, ECO:0000269|PubMed:11438732}. | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000262189, ENST00000355193, ENST00000485241, ENST00000485655, | ENST00000489094, ENST00000265755, ENST00000424337, ENST00000455841, ENST00000476977, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 26 X 23 X 12=7176 | 12 X 10 X 9=1080 |
| # samples | 32 | 12 | |
| ** MAII score | log2(32/7176*10)=-4.4870360800319 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(12/1080*10)=-3.16992500144231 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Fusion gene context | PubMed: KMT2C [Title/Abstract] AND GTF2IRD1 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Fusion neoantigen context | PubMed: KMT2C [Title/Abstract] AND GTF2IRD1 [Title/Abstract] AND neoantigen [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | KMT2C(151902191)-GTF2IRD1(74004180), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | KMT2C-GTF2IRD1 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. KMT2C-GTF2IRD1 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. KMT2C-GTF2IRD1 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. KMT2C-GTF2IRD1 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) |
| 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 | KMT2C | GO:0097692 | histone H3-K4 monomethylation | 26324722 |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr7:151902191/chr7:74004180) - 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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| Retention analysis results 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, are available here. |
| Fusion gene breakpoints across KMT2C (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 GTF2IRD1 (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 Amino Acid Sequences |
| 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) |
| ENST00000262189 | KMT2C | chr7 | 151902191 | - | ENST00000265755 | GTF2IRD1 | chr7 | 74004180 | + | 4852 | 4180 | 207 | 4694 | 1495 |
| ENST00000262189 | KMT2C | chr7 | 151902191 | - | ENST00000455841 | GTF2IRD1 | chr7 | 74004180 | + | 4866 | 4180 | 207 | 4694 | 1495 |
| ENST00000262189 | KMT2C | chr7 | 151902191 | - | ENST00000424337 | GTF2IRD1 | chr7 | 74004180 | + | 4863 | 4180 | 207 | 4694 | 1495 |
| ENST00000262189 | KMT2C | chr7 | 151902191 | - | ENST00000476977 | GTF2IRD1 | chr7 | 74004180 | + | 6037 | 4180 | 207 | 4742 | 1511 |
| ENST00000355193 | KMT2C | chr7 | 151902191 | - | ENST00000265755 | GTF2IRD1 | chr7 | 74004180 | + | 4852 | 4180 | 207 | 4694 | 1495 |
| ENST00000355193 | KMT2C | chr7 | 151902191 | - | ENST00000455841 | GTF2IRD1 | chr7 | 74004180 | + | 4866 | 4180 | 207 | 4694 | 1495 |
| ENST00000355193 | KMT2C | chr7 | 151902191 | - | ENST00000424337 | GTF2IRD1 | chr7 | 74004180 | + | 4863 | 4180 | 207 | 4694 | 1495 |
| ENST00000355193 | KMT2C | chr7 | 151902191 | - | ENST00000476977 | GTF2IRD1 | chr7 | 74004180 | + | 6037 | 4180 | 207 | 4742 | 1511 |
| 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 |
| ENST00000262189 | ENST00000265755 | KMT2C | chr7 | 151902191 | - | GTF2IRD1 | chr7 | 74004180 | + | 0.00048346 | 0.9995165 |
| ENST00000262189 | ENST00000455841 | KMT2C | chr7 | 151902191 | - | GTF2IRD1 | chr7 | 74004180 | + | 0.000454385 | 0.99954563 |
| ENST00000262189 | ENST00000424337 | KMT2C | chr7 | 151902191 | - | GTF2IRD1 | chr7 | 74004180 | + | 0.000460743 | 0.99953926 |
| ENST00000262189 | ENST00000476977 | KMT2C | chr7 | 151902191 | - | GTF2IRD1 | chr7 | 74004180 | + | 0.000526894 | 0.99947315 |
| ENST00000355193 | ENST00000265755 | KMT2C | chr7 | 151902191 | - | GTF2IRD1 | chr7 | 74004180 | + | 0.00048346 | 0.9995165 |
| ENST00000355193 | ENST00000455841 | KMT2C | chr7 | 151902191 | - | GTF2IRD1 | chr7 | 74004180 | + | 0.000454385 | 0.99954563 |
| ENST00000355193 | ENST00000424337 | KMT2C | chr7 | 151902191 | - | GTF2IRD1 | chr7 | 74004180 | + | 0.000460743 | 0.99953926 |
| ENST00000355193 | ENST00000476977 | KMT2C | chr7 | 151902191 | - | GTF2IRD1 | chr7 | 74004180 | + | 0.000526894 | 0.99947315 |
| Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones. |
Get the fusion protein sequences from here. |
| Fusion protein sequence information is available in the fasta format. >FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP |
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Fusion Protein Breakpoint Sequences for KMT2C-GTF2IRD1 |
| +/-13 AA sequence from the breakpoints of the fusion protein sequences. |
| Hgene | Hchr | Hbp | Tgene | Tchr | Tbp | Length(fusion protein) | BP in fusion protein | Peptide |
| KMT2C | chr7 | 151902191 | GTF2IRD1 | chr7 | 74004180 | 4180 | 1324 | SGSISEQLPCRDDDEDDANRLGEKVI |
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Potential FusionNeoAntigen Information of KMT2C-GTF2IRD1 in HLA I |
| Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific. |
| Potential FusionNeoAntigen Information * We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5) |
| Fusion gene | Hchr | Hbp | Tgene | Tchr | Tbp | HLA I | FusionNeoAntigen peptide | Binding score | Immunogenic score | Neoantigen start (at BP 13) | Neoantigen end (at BP 13) |
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Potential FusionNeoAntigen Information of KMT2C-GTF2IRD1 in HLA II |
| Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific. |
| Potential FusionNeoAntigen Information * We used NetMHCIIpan v4.1 (%rank<0.5). |
| Fusion gene | Hchr | Hbp | Tgene | Tchr | Tbp | HLA II | FusionNeoAntigen peptide | Neoantigen start (at BP 13) | Neoantigen end (at BP 13) |
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Fusion breakpoint peptide structures of KMT2C-GTF2IRD1 |
| 3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens * The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA. |
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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of KMT2C-GTF2IRD1 |
| Virtual screening between 25 HLAs (from PDB) and FusionNeoAntigens * We used Glide to predict the interaction between HLAs and neoantigens. |
| HLA allele | PDB ID | File name | BPseq | Docking score | Glide score |
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Vaccine Design for the FusionNeoAntigens of KMT2C-GTF2IRD1 |
| mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is. |
| Fusion gene | Hchr | Hbp | Tchr | Tbp | Start in +/-13AA | End in +/-13AA | FusionNeoAntigen peptide sequence | FusionNeoAntigen RNA sequence |
| mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs. |
| Fusion gene | Hchr | Hbp | Tchr | Tbp | Start in +/-13AA | End in +/-13AA | FusionNeoAntigen peptide | FusionNEoAntigen RNA sequence |
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Information of the samples that have these potential fusion neoantigens of KMT2C-GTF2IRD1 |
| These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens. |
| Cancer type | Fusion gene | Hchr | Hbp | Henst | Tchr | Tbp | Tenst | Sample |
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Potential target of CAR-T therapy development for KMT2C-GTF2IRD1 |
| Predicted 3D structure. We used RoseTTAFold. |
| 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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features * Minus value of BPloci means that the break point is located before the CDS. |
| - In-frame and retained 'Transmembrane'. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
| Subcellular localization prediction of the transmembrane domain retained fusion proteins * We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image. |
| Hgene | Hchr | Hbp | Henst | Tgene | Tchr | Tbp | Tenst | DeepLoc result |
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Related Drugs to KMT2C-GTF2IRD1 |
| 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 KMT2C-GTF2IRD1 |
| 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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