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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:CCDC22-FOXP3 (FusionGDB2 ID:13795) |
Fusion Gene Summary for CCDC22-FOXP3 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: CCDC22-FOXP3 | Fusion gene ID: 13795 | Hgene | Tgene | Gene symbol | CCDC22 | FOXP3 | Gene ID | 28952 | 50943 |
| Gene name | coiled-coil domain containing 22 | forkhead box P3 | |
| Synonyms | CXorf37|JM1|RTSC2 | AIID|DIETER|IPEX|JM2|PIDX|XPID | |
| Cytomap | Xp11.23 | Xp11.23 | |
| Type of gene | protein-coding | protein-coding | |
| Description | coiled-coil domain-containing protein 22 | forkhead box protein P3FOXP3delta7immune dysregulation, polyendocrinopathy, enteropathy, X-linkedimmunodeficiency, polyendocrinopathy, enteropathy, X-linkedscurfin | |
| Modification date | 20200313 | 20200327 | |
| UniProtAcc | O60826 | . | |
| Ensembl transtripts involved in fusion gene | ENST00000376227, ENST00000496651, | ENST00000376207, ENST00000376199, ENST00000557224, ENST00000455775, ENST00000518685, ENST00000376197, | |
| Fusion gene scores | * DoF score | 2 X 2 X 2=8 | 1 X 1 X 1=1 |
| # samples | 2 | 1 | |
| ** MAII score | log2(2/8*10)=1.32192809488736 | log2(1/1*10)=3.32192809488736 | |
| Context | PubMed: CCDC22 [Title/Abstract] AND FOXP3 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint | CCDC22(49103386)-FOXP3(49112263), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | CCDC22-FOXP3 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. CCDC22-FOXP3 seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted ORF. CCDC22-FOXP3 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF. CCDC22-FOXP3 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor 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 |
| Tgene | FOXP3 | GO:0002725 | negative regulation of T cell cytokine production | 15466453 |
| Tgene | FOXP3 | GO:0008285 | negative regulation of cell proliferation | 15652505 |
| Tgene | FOXP3 | GO:0032088 | negative regulation of NF-kappaB transcription factor activity | 16652169 |
| Tgene | FOXP3 | GO:0032689 | negative regulation of interferon-gamma production | 15466453 |
| Tgene | FOXP3 | GO:0032693 | negative regulation of interleukin-10 production | 15466453 |
| Tgene | FOXP3 | GO:0032703 | negative regulation of interleukin-2 production | 15466453|17360565|17377532 |
| Tgene | FOXP3 | GO:0032713 | negative regulation of interleukin-4 production | 15466453 |
| Tgene | FOXP3 | GO:0032792 | negative regulation of CREB transcription factor activity | 16652169 |
| Tgene | FOXP3 | GO:0042036 | negative regulation of cytokine biosynthetic process | 11483607 |
| Tgene | FOXP3 | GO:0042110 | T cell activation | 15466453 |
| Tgene | FOXP3 | GO:0042130 | negative regulation of T cell proliferation | 15466453 |
| Tgene | FOXP3 | GO:0043433 | negative regulation of DNA-binding transcription factor activity | 16873067 |
| Tgene | FOXP3 | GO:0045892 | negative regulation of transcription, DNA-templated | 11483607|16920951|17360565|22678915 |
| Tgene | FOXP3 | GO:0045893 | positive regulation of transcription, DNA-templated | 15466453 |
| Tgene | FOXP3 | GO:0050710 | negative regulation of cytokine secretion | 11483607 |
| Tgene | FOXP3 | GO:0050777 | negative regulation of immune response | 15652505 |
| Fusion gene breakpoints across CCDC22 (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 FOXP3 (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 |
| ChimerDB4 | LUAD | TCGA-55-1592-01A | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
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Fusion Gene ORF analysis for CCDC22-FOXP3 |
| 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 |
| Frame-shift | ENST00000376227 | ENST00000376207 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| Frame-shift | ENST00000376227 | ENST00000376199 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| Frame-shift | ENST00000376227 | ENST00000557224 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| Frame-shift | ENST00000376227 | ENST00000455775 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| Frame-shift | ENST00000376227 | ENST00000518685 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| Frame-shift | ENST00000376227 | ENST00000376197 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| intron-3CDS | ENST00000496651 | ENST00000376207 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| intron-3CDS | ENST00000496651 | ENST00000376199 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| intron-3CDS | ENST00000496651 | ENST00000557224 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| intron-3CDS | ENST00000496651 | ENST00000455775 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| intron-3CDS | ENST00000496651 | ENST00000518685 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| intron-3CDS | ENST00000496651 | ENST00000376197 | CCDC22 | chrX | 49103386 | + | FOXP3 | chrX | 49112263 | - |
| 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 CCDC22-FOXP3 |
| 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 CCDC22-FOXP3 |
| 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 |
| CCDC22 | . |
| FUNCTION: Involved in regulation of NF-kappa-B signaling. Promotes ubiquitination of I-kappa-B-kinase subunit IKBKB and its subsequent proteasomal degradation leading to NF-kappa-B activation; the function may involve association with COMMD8 and a CUL1-dependent E3 ubiquitin ligase complex. May down-regulate NF-kappa-B activity via association with COMMD1 and involving a CUL2-dependent E3 ubiquitin ligase complex. Regulates the cellular localization of COMM domain-containing proteins, such as COMMD1 and COMMD10 (PubMed:23563313). Component of the CCC complex, which is involved in the regulation of endosomal recycling of surface proteins, including integrins, signaling receptor and channels. The CCC complex associates with SNX17, retriever and WASH complexes to prevent lysosomal degradation and promote cell surface recycling of numerous cargos such as integrins ITGA5:ITGB1 (PubMed:28892079, PubMed:25355947). Plays a role in copper ion homeostasis. Involved in copper-dependent ATP7A trafficking between the trans-Golgi network and vesicles in the cell periphery; the function is proposed to depend on its association within the CCC complex and cooperation with the WASH complex on early endosomes (PubMed:25355947). {ECO:0000269|PubMed:23563313, ECO:0000269|PubMed:25355947, ECO:0000269|PubMed:28892079}.; FUNCTION: (Microbial infection) The CCC complex, in collaboration with the heterotrimeric retriever complex, mediates the exit of human papillomavirus to the cell surface. {ECO:0000269|PubMed:28892079}. | FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes. |
| 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 CCDC22-FOXP3 |
| 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 CCDC22-FOXP3 |
| 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 CCDC22-FOXP3 |
| 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 CCDC22-FOXP3 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | CCDC22 | C4225419 | RITSCHER-SCHINZEL SYNDROME 2 | 3 | UNIPROT |
| Hgene | CCDC22 | C0796137 | 3C syndrome | 1 | CTD_human;ORPHANET |
| Tgene | FOXP3 | C0342288 | Insulin-dependent diabetes mellitus secretory diarrhea syndrome | 13 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
| Tgene | FOXP3 | C0003873 | Rheumatoid Arthritis | 1 | CTD_human |
| Tgene | FOXP3 | C0005586 | Bipolar Disorder | 1 | PSYGENET |
| Tgene | FOXP3 | C0006142 | Malignant neoplasm of breast | 1 | CTD_human |
| Tgene | FOXP3 | C0020305 | Hydrops Fetalis | 1 | GENOMICS_ENGLAND |
| Tgene | FOXP3 | C0023493 | Adult T-Cell Lymphoma/Leukemia | 1 | CTD_human |
| Tgene | FOXP3 | C0028796 | Dermatitis, Occupational | 1 | CTD_human |
| Tgene | FOXP3 | C0032460 | Polycystic Ovary Syndrome | 1 | CTD_human |
| Tgene | FOXP3 | C0086457 | Industrial Dermatosis | 1 | CTD_human |
| Tgene | FOXP3 | C0678222 | Breast Carcinoma | 1 | CTD_human |
| Tgene | FOXP3 | C1136382 | Sclerocystic Ovaries | 1 | CTD_human |
| Tgene | FOXP3 | C1257931 | Mammary Neoplasms, Human | 1 | CTD_human |
| Tgene | FOXP3 | C1458155 | Mammary Neoplasms | 1 | CTD_human |
| Tgene | FOXP3 | C4704874 | Mammary Carcinoma, Human | 1 | CTD_human |
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