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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:ARID2-CCND2 (FusionGDB2 ID:HG196528TG894) |
Fusion Gene Summary for ARID2-CCND2 |
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Fusion gene information | Fusion gene name: ARID2-CCND2 | Fusion gene ID: hg196528tg894 | Hgene | Tgene | Gene symbol | ARID2 | CCND2 | Gene ID | 196528 | 894 |
Gene name | AT-rich interaction domain 2 | cyclin D2 | |
Synonyms | BAF200|CSS6|p200 | KIAK0002|MPPH3 | |
Cytomap | ('ARID2')('CCND2') 12q12 | 12p13.32 | |
Type of gene | protein-coding | protein-coding | |
Description | AT-rich interactive domain-containing protein 2ARID domain-containing protein 2AT rich interactive domain 2 (ARID, RFX-like)BRG1-associated factor 200zinc finger protein with activation potentialzipzap/p200 | G1/S-specific cyclin-D2 | |
Modification date | 20200320 | 20200313 | |
UniProtAcc | . | P30279 | |
Ensembl transtripts involved in fusion gene | ENST00000334344, ENST00000422737, ENST00000444670, ENST00000457135, ENST00000479608, | ||
Fusion gene scores | * DoF score | 17 X 9 X 12=1836 | 4 X 6 X 3=72 |
# samples | 17 | 6 | |
** MAII score | log2(17/1836*10)=-3.43295940727611 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(6/72*10)=-0.263034405833794 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ARID2 [Title/Abstract] AND CCND2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | ARID2(46125097)-CCND2(4383167), # 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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | ARID2 | GO:0006337 | nucleosome disassembly | 8895581 |
Hgene | ARID2 | GO:0008285 | negative regulation of cell proliferation | 26169693 |
Hgene | ARID2 | GO:0030336 | negative regulation of cell migration | 26169693 |
Tgene | CCND2 | GO:0001934 | positive regulation of protein phosphorylation | 8114739 |
Tgene | CCND2 | GO:0045737 | positive regulation of cyclin-dependent protein serine/threonine kinase activity | 8114739 |
![]() * 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 | GBM | TCGA-06-0129-01A | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
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Fusion Gene ORF analysis for ARID2-CCND2 |
![]() * 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 |
5CDS-5UTR | ENST00000334344 | ENST00000261254 | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
5CDS-intron | ENST00000334344 | ENST00000541542 | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
5UTR-5UTR | ENST00000422737 | ENST00000261254 | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
5UTR-intron | ENST00000422737 | ENST00000541542 | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
intron-5UTR | ENST00000444670 | ENST00000261254 | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
intron-5UTR | ENST00000457135 | ENST00000261254 | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
intron-5UTR | ENST00000479608 | ENST00000261254 | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
intron-intron | ENST00000444670 | ENST00000541542 | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
intron-intron | ENST00000457135 | ENST00000541542 | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
intron-intron | ENST00000479608 | ENST00000541542 | ARID2 | chr12 | 46125097 | + | CCND2 | chr12 | 4383167 | + |
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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) |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
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Fusion Genomic Features for ARID2-CCND2 |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
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Fusion Protein Features for ARID2-CCND2 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:46125097/:4383167) - 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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Hgene | Tgene |
. | CCND2 |
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. | FUNCTION: Regulatory component of the cyclin D2-CDK4 (DC) complex that phosphorylates and inhibits members of the retinoblastoma (RB) protein family including RB1 and regulates the cell-cycle during G(1)/S transition. Phosphorylation of RB1 allows dissociation of the transcription factor E2F from the RB/E2F complex and the subsequent transcription of E2F target genes which are responsible for the progression through the G(1) phase. Hypophosphorylates RB1 in early G(1) phase. Cyclin D-CDK4 complexes are major integrators of various mitogenenic and antimitogenic signals. Also substrate for SMAD3, phosphorylating SMAD3 in a cell-cycle-dependent manner and repressing its transcriptional activity. Component of the ternary complex, cyclin D2/CDK4/CDKN1B, required for nuclear translocation and activity of the cyclin D-CDK4 complex (By similarity). {ECO:0000250}. |
![]() * 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 ARID2-CCND2 |
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Fusion Gene PPI Analysis for ARID2-CCND2 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for ARID2-CCND2 |
![]() (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 ARID2-CCND2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ARID2 | C2239176 | Liver carcinoma | 2 | CGI;CTD_human |
Hgene | ARID2 | C0033578 | Prostatic Neoplasms | 1 | CTD_human |
Hgene | ARID2 | C0265338 | Coffin-Siris syndrome | 1 | ORPHANET |
Hgene | ARID2 | C0376358 | Malignant neoplasm of prostate | 1 | CTD_human |
Tgene | C1863924 | Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome | 2 | CTD_human;ORPHANET | |
Tgene | C0007102 | Malignant tumor of colon | 1 | CTD_human | |
Tgene | C0009375 | Colonic Neoplasms | 1 | CTD_human | |
Tgene | C0009402 | Colorectal Carcinoma | 1 | CTD_human | |
Tgene | C0009404 | Colorectal Neoplasms | 1 | CTD_human | |
Tgene | C0009451 | Communicating Hydrocephalus | 1 | CTD_human | |
Tgene | C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | 1 | CTD_human | |
Tgene | C0016059 | Fibrosis | 1 | CTD_human | |
Tgene | C0018800 | Cardiomegaly | 1 | CTD_human | |
Tgene | C0020255 | Hydrocephalus | 1 | CTD_human | |
Tgene | C0020256 | Congenital Hydrocephalus | 1 | CTD_human | |
Tgene | C0023467 | Leukemia, Myelocytic, Acute | 1 | CTD_human | |
Tgene | C0026998 | Acute Myeloid Leukemia, M1 | 1 | CTD_human | |
Tgene | C0033578 | Prostatic Neoplasms | 1 | CTD_human | |
Tgene | C0036341 | Schizophrenia | 1 | PSYGENET | |
Tgene | C0151744 | Myocardial Ischemia | 1 | CTD_human | |
Tgene | C0152427 | Polydactyly | 1 | GENOMICS_ENGLAND | |
Tgene | C0220697 | POLYDACTYLY, POSTAXIAL | 1 | CTD_human | |
Tgene | C0221355 | Macrocephaly | 1 | CTD_human | |
Tgene | C0270720 | Hydrocephalus Ex-Vacuo | 1 | CTD_human | |
Tgene | C0376358 | Malignant neoplasm of prostate | 1 | CTD_human | |
Tgene | C0477432 | Post-Traumatic Hydrocephalus | 1 | CTD_human | |
Tgene | C0549423 | Obstructive Hydrocephalus | 1 | CTD_human | |
Tgene | C0919267 | ovarian neoplasm | 1 | CTD_human | |
Tgene | C1140680 | Malignant neoplasm of ovary | 1 | CTD_human | |
Tgene | C1383860 | Cardiac Hypertrophy | 1 | CTD_human | |
Tgene | C1531647 | Cerebral ventriculomegaly | 1 | CTD_human | |
Tgene | C1623038 | Cirrhosis | 1 | CTD_human | |
Tgene | C1845668 | Perisylvian syndrome | 1 | CTD_human | |
Tgene | C1868120 | POSTAXIAL POLYDACTYLY, TYPE B | 1 | CTD_human | |
Tgene | C1879321 | Acute Myeloid Leukemia (AML-M2) | 1 | CTD_human | |
Tgene | C1879677 | Alcohol Toxicity | 1 | PSYGENET | |
Tgene | C2936718 | Fetal Cerebral Ventriculomegaly | 1 | CTD_human | |
Tgene | C2936786 | Aqueductal Stenosis | 1 | CTD_human | |
Tgene | C3887487 | Postaxial polydactyly type A | 1 | CTD_human | |
Tgene | C4014742 | MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 | 1 | GENOMICS_ENGLAND;UNIPROT | |
Tgene | C4282400 | Polydactyly, Postaxial, Type A1 | 1 | CTD_human |