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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:CHD1-RUNX1 (FusionGDB2 ID:HG1105TG861) |
Fusion Gene Summary for CHD1-RUNX1 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: CHD1-RUNX1 | Fusion gene ID: hg1105tg861 | Hgene | Tgene | Gene symbol | CHD1 | RUNX1 | Gene ID | 1105 | 861 |
| Gene name | chromodomain helicase DNA binding protein 1 | RUNX family transcription factor 1 | |
| Synonyms | CHD-1|PILBOS | AML1|AML1-EVI-1|AMLCR1|CBF2alpha|CBFA2|EVI-1|PEBP2aB|PEBP2alpha | |
| Cytomap | ('CHD1')('RUNX1') 5q15-q21.1 | 21q22.12 | |
| Type of gene | protein-coding | protein-coding | |
| Description | chromodomain-helicase-DNA-binding protein 1ATP-dependent helicase CHD1 | runt-related transcription factor 1AML1-EVI-1 fusion proteinPEA2-alpha BPEBP2-alpha BSL3-3 enhancer factor 1 alpha B subunitSL3/AKV core-binding factor alpha B subunitacute myeloid leukemia 1 proteincore-binding factor, runt domain, alpha subunit 2 | |
| Modification date | 20200313 | 20200322 | |
| UniProtAcc | O14646 | Q01196 | |
| Ensembl transtripts involved in fusion gene | ENST00000284049, ENST00000511067, | ||
| Fusion gene scores | * DoF score | 14 X 15 X 8=1680 | 36 X 59 X 13=27612 |
| # samples | 19 | 63 | |
| ** MAII score | log2(19/1680*10)=-3.14438990933518 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(63/27612*10)=-5.45379975055797 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: CHD1 [Title/Abstract] AND RUNX1 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint | |||
| 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 | RUNX1 | GO:0030097 | hemopoiesis | 21873977 |
| Tgene | RUNX1 | GO:0045893 | positive regulation of transcription, DNA-templated | 10207087|14970218 |
| Tgene | RUNX1 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 9199349|10207087|14970218|21873977 |
| Fusion gene information * 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 |
| ChimerKB4 | . | . | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| ChimerKB4 | . | . | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
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Fusion Gene ORF analysis for CHD1-RUNX1 |
| 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-intron | ENST00000284049 | ENST00000300305 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000284049 | ENST00000300305 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000284049 | ENST00000325074 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000284049 | ENST00000325074 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000284049 | ENST00000344691 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000284049 | ENST00000344691 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000284049 | ENST00000358356 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000284049 | ENST00000358356 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000284049 | ENST00000399240 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000284049 | ENST00000399240 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000284049 | ENST00000437180 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000284049 | ENST00000437180 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000284049 | ENST00000486278 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000284049 | ENST00000486278 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000284049 | ENST00000494829 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000284049 | ENST00000494829 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000511067 | ENST00000300305 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000511067 | ENST00000300305 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000511067 | ENST00000325074 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000511067 | ENST00000325074 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000511067 | ENST00000344691 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000511067 | ENST00000344691 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000511067 | ENST00000358356 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000511067 | ENST00000358356 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000511067 | ENST00000399240 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000511067 | ENST00000399240 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000511067 | ENST00000437180 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000511067 | ENST00000437180 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000511067 | ENST00000486278 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000511067 | ENST00000486278 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| intron-intron | ENST00000511067 | ENST00000494829 | CHD1 | chr5 | 98208259 | - | RUNX1 | chr21 | 98208259 | - |
| intron-intron | ENST00000511067 | ENST00000494829 | CHD1 | chr5 | 98209427 | - | RUNX1 | chr21 | 98209427 | - |
| 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 CHD1-RUNX1 |
| 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) |
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Fusion Protein Features for CHD1-RUNX1 |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:/:) - 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 |
| CHD1 | RUNX1 |
| FUNCTION: ATP-dependent chromatin-remodeling factor which functions as substrate recognition component of the transcription regulatory histone acetylation (HAT) complex SAGA. Regulates polymerase II transcription. Also required for efficient transcription by RNA polymerase I, and more specifically the polymerase I transcription termination step. Regulates negatively DNA replication. Not only involved in transcription-related chromatin-remodeling, but also required to maintain a specific chromatin configuration across the genome. Is also associated with histone deacetylase (HDAC) activity (By similarity). Required for the bridging of SNF2, the FACT complex, the PAF complex as well as the U2 snRNP complex to H3K4me3. Functions to modulate the efficiency of pre-mRNA splicing in part through physical bridging of spliceosomal components to H3K4me3 (PubMed:18042460, PubMed:28866611). Required for maintaining open chromatin and pluripotency in embryonic stem cells (By similarity). {ECO:0000250|UniProtKB:P40201, ECO:0000269|PubMed:18042460, ECO:0000269|PubMed:28866611}. | FUNCTION: Forms the heterodimeric complex core-binding factor (CBF) with CBFB. RUNX members modulate the transcription of their target genes through recognizing the core consensus binding sequence 5'-TGTGGT-3', or very rarely, 5'-TGCGGT-3', within their regulatory regions via their runt domain, while CBFB is a non-DNA-binding regulatory subunit that allosterically enhances the sequence-specific DNA-binding capacity of RUNX. The heterodimers bind to the core site of a number of enhancers and promoters, including murine leukemia virus, polyomavirus enhancer, T-cell receptor enhancers, LCK, IL3 and GM-CSF promoters (Probable). Essential for the development of normal hematopoiesis (PubMed:17431401). Acts synergistically with ELF4 to transactivate the IL-3 promoter and with ELF2 to transactivate the BLK promoter (PubMed:10207087, PubMed:14970218). Inhibits KAT6B-dependent transcriptional activation (By similarity). Involved in lineage commitment of immature T cell precursors. CBF complexes repress ZBTB7B transcription factor during cytotoxic (CD8+) T cell development. They bind to RUNX-binding sequence within the ZBTB7B locus acting as transcriptional silencer and allowing for cytotoxic T cell differentiation. CBF complexes binding to the transcriptional silencer is essential for recruitment of nuclear protein complexes that catalyze epigenetic modifications to establish epigenetic ZBTB7B silencing (By similarity). Controls the anergy and suppressive function of regulatory T-cells (Treg) by associating with FOXP3. Activates the expression of IL2 and IFNG and down-regulates the expression of TNFRSF18, IL2RA and CTLA4, in conventional T-cells (PubMed:17377532). Positively regulates the expression of RORC in T-helper 17 cells (By similarity). {ECO:0000250|UniProtKB:Q03347, ECO:0000269|PubMed:10207087, ECO:0000269|PubMed:11965546, ECO:0000269|PubMed:14970218, ECO:0000269|PubMed:17377532, ECO:0000269|PubMed:17431401, ECO:0000305}.; FUNCTION: Isoform AML-1G shows higher binding activities for target genes and binds TCR-beta-E2 and RAG-1 target site with threefold higher affinity than other isoforms. It is less effective in the context of neutrophil terminal differentiation. {ECO:0000250|UniProtKB:Q03347}.; FUNCTION: Isoform AML-1L interferes with the transactivation activity of RUNX1. {ECO:0000269|PubMed:9199349}. |
| 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 CHD1-RUNX1 |
| 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 CHD1-RUNX1 |
| 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 CHD1-RUNX1 |
| 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 CHD1-RUNX1 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | CHD1 | C0009402 | Colorectal Carcinoma | 1 | CTD_human |
| Hgene | CHD1 | C0009404 | Colorectal Neoplasms | 1 | CTD_human |
| Hgene | CHD1 | C0025261 | Memory Disorders | 1 | CTD_human |
| Hgene | CHD1 | C0033578 | Prostatic Neoplasms | 1 | CTD_human |
| Hgene | CHD1 | C0233794 | Memory impairment | 1 | CTD_human |
| Hgene | CHD1 | C0376358 | Malignant neoplasm of prostate | 1 | CTD_human |
| Hgene | CHD1 | C0751292 | Age-Related Memory Disorders | 1 | CTD_human |
| Hgene | CHD1 | C0751293 | Memory Disorder, Semantic | 1 | CTD_human |
| Hgene | CHD1 | C0751294 | Memory Disorder, Spatial | 1 | CTD_human |
| Hgene | CHD1 | C0751295 | Memory Loss | 1 | CTD_human |
| Hgene | CHD1 | C4540131 | PILAROWSKI-BJORNSSON SYNDROME | 1 | GENOMICS_ENGLAND;ORPHANET;UNIPROT |
| Tgene | C1832388 | Platelet Disorder, Familial, with Associated Myeloid Malignancy | 11 | CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT | |
| Tgene | C0023467 | Leukemia, Myelocytic, Acute | 4 | CGI;CTD_human;GENOMICS_ENGLAND | |
| Tgene | C0026998 | Acute Myeloid Leukemia, M1 | 3 | CTD_human | |
| Tgene | C1879321 | Acute Myeloid Leukemia (AML-M2) | 3 | CTD_human | |
| Tgene | C0023485 | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma | 2 | CTD_human | |
| Tgene | C0003873 | Rheumatoid Arthritis | 1 | CTD_human | |
| Tgene | C0006413 | Burkitt Lymphoma | 1 | ORPHANET | |
| Tgene | C0017636 | Glioblastoma | 1 | CTD_human | |
| Tgene | C0023452 | Childhood Acute Lymphoblastic Leukemia | 1 | CTD_human | |
| Tgene | C0023453 | L2 Acute Lymphoblastic Leukemia | 1 | CTD_human | |
| Tgene | C0023473 | Myeloid Leukemia, Chronic | 1 | ORPHANET | |
| Tgene | C0033578 | Prostatic Neoplasms | 1 | CTD_human | |
| Tgene | C0040034 | Thrombocytopenia | 1 | GENOMICS_ENGLAND | |
| Tgene | C0334588 | Giant Cell Glioblastoma | 1 | CTD_human | |
| Tgene | C0349639 | Juvenile Myelomonocytic Leukemia | 1 | CTD_human | |
| Tgene | C0376358 | Malignant neoplasm of prostate | 1 | CTD_human | |
| Tgene | C1292769 | Precursor B-cell lymphoblastic leukemia | 1 | ORPHANET | |
| Tgene | C1621958 | Glioblastoma Multiforme | 1 | CTD_human | |
| Tgene | C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | 1 | CTD_human | |
| Tgene | C2713368 | Hematopoetic Myelodysplasia | 1 | CTD_human | |
| Tgene | C3463824 | MYELODYSPLASTIC SYNDROME | 1 | CTD_human |
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