![]() |
||||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Fusion gene ID: 30668 |
FusionGeneSummary for RBFOX3_RYR2 |
![]() |
Fusion gene information | Fusion gene name: RBFOX3_RYR2 | Fusion gene ID: 30668 | Hgene | Tgene | Gene symbol | RBFOX3 | RYR2 | Gene ID | 146713 | 6262 |
Gene name | RNA binding fox-1 homolog 3 | ryanodine receptor 2 | |
Synonyms | FOX-3|FOX3|HRNBP3|NEUN | ARVC2|ARVD2|RYR-2|RyR|VTSIP | |
Cytomap | 17q25.3 | 1q43 | |
Type of gene | protein-coding | protein-coding | |
Description | RNA binding protein fox-1 homolog 3RNA binding protein, fox-1 homolog 3fox-1 homolog Chexaribonucleotide binding protein 3neuN antigenneuronal nuclei antigen | ryanodine receptor 2cardiac muscle ryanodine receptor-calcium release channelcardiac-type ryanodine receptorislet-type ryanodine receptorkidney-type ryanodine receptorryanodine receptor 2 (cardiac)type 2 ryanodine receptor | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | A6NFN3 | Q92736 | |
Ensembl transtripts involved in fusion gene | ENST00000453134, ENST00000583458, ENST00000415831, ENST00000582043, ENST00000580155, ENST00000584778, ENST00000578887, | ENST00000366574, ENST00000360064, ENST00000542537, ENST00000609119, | |
Fusion gene scores | * DoF score | 2 X 2 X 1=4 | 5 X 5 X 2=50 |
# samples | 2 | 7 | |
** MAII score | log2(2/4*10)=2.32192809488736 | log2(7/50*10)=0.485426827170242 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: RBFOX3 [Title/Abstract] AND RYR2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
![]() |
Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | RYR2 | GO:0005513 | detection of calcium ion | 10830164 |
Tgene | RYR2 | GO:0006816 | calcium ion transport | 17921453 |
Tgene | RYR2 | GO:0031000 | response to caffeine | 17921453 |
Tgene | RYR2 | GO:0035584 | calcium-mediated signaling using intracellular calcium source | 17921453 |
Tgene | RYR2 | GO:0051209 | release of sequestered calcium ion into cytosol | 12443530|17921453 |
Tgene | RYR2 | GO:0051284 | positive regulation of sequestering of calcium ion | 12443530|12919952 |
Tgene | RYR2 | GO:0051775 | response to redox state | 19226252 |
Tgene | RYR2 | GO:0060402 | calcium ion transport into cytosol | 17921453 |
Tgene | RYR2 | GO:0071313 | cellular response to caffeine | 12919952 |
Tgene | RYR2 | GO:0072599 | establishment of protein localization to endoplasmic reticulum | 12443530 |
Tgene | RYR2 | GO:1901896 | positive regulation of calcium-transporting ATPase activity | 12443530 |
![]() (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * 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. |
Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChiTaRS3.1 | CR748559 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * 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 | ENST00000453134 | ENST00000366574 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000453134 | ENST00000360064 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000453134 | ENST00000542537 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000453134 | ENST00000609119 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000583458 | ENST00000366574 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000583458 | ENST00000360064 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000583458 | ENST00000542537 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000583458 | ENST00000609119 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000415831 | ENST00000366574 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000415831 | ENST00000360064 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000415831 | ENST00000542537 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000415831 | ENST00000609119 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000582043 | ENST00000366574 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000582043 | ENST00000360064 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000582043 | ENST00000542537 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000582043 | ENST00000609119 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000580155 | ENST00000366574 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000580155 | ENST00000360064 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000580155 | ENST00000542537 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000580155 | ENST00000609119 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000584778 | ENST00000366574 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000584778 | ENST00000360064 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000584778 | ENST00000542537 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000584778 | ENST00000609119 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000578887 | ENST00000366574 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000578887 | ENST00000360064 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000578887 | ENST00000542537 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
intron-intron | ENST00000578887 | ENST00000609119 | RBFOX3 | chr17 | 77111712 | - | RYR2 | chr1 | 237431970 | - |
Top |
FusionProtFeatures for RBFOX3_RYR2 |
![]() |
Hgene | Tgene |
RBFOX3 | RYR2 |
Pre-mRNA alternative splicing regulator. Regulatesalternative splicing of RBFOX2 to enhance the production of mRNAspecies that are targeted for nonsense-mediated decay (NMD).{ECO:0000250|UniProtKB:Q8BIF2}. | Calcium channel that mediates the release of Ca(2+) fromthe sarcoplasmic reticulum into the cytoplasm and thereby plays akey role in triggering cardiac muscle contraction. Aberrantchannel activation can lead to cardiac arrhythmia. In cardiacmyocytes, calcium release is triggered by increased Ca(2+) levelsdue to activation of the L-type calcium channel CACNA1C. Thecalcium channel activity is modulated by formation ofheterotetramers with RYR3. Required for cellular calcium ionhomeostasis. Required for embryonic heart development.{ECO:0000269|PubMed:10830164, ECO:0000269|PubMed:20056922,ECO:0000269|PubMed:27733687}. |
![]() * 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 |
Top |
FusionGeneSequence for RBFOX3_RYR2 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
* Fusion transcript sequences (only coding sequence (CDS) region). |
* Fusion transcript sequences (Full-length transcript). |
Top |
FusionGenePPI for RBFOX3_RYR2 |
![]() |
![]() |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Top |
RelatedDrugs for RBFOX3_RYR2 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | RYR2 | Q92736 | DB09085 | Tetracaine | Ryanodine receptor 2 | small molecule | approved|vet_approved |
Top |
RelatedDiseases for RBFOX3_RYR2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | RYR2 | C1631597 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) | 12 | CTD_human;ORPHANET;UNIPROT |
Tgene | RYR2 | C0042514 | Tachycardia, Ventricular | 2 | CTD_human;HPO |
Tgene | RYR2 | C1832931 | ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2 | 2 | CTD_human;UNIPROT |
Tgene | RYR2 | C0039231 | Tachycardia | 1 | CTD_human |
Tgene | RYR2 | C0151744 | Myocardial Ischemia | 1 | CTD_human |
Tgene | RYR2 | C0345967 | Malignant mesothelioma | 1 | CTD_human |
Tgene | RYR2 | C0853897 | Diabetic Cardiomyopathies | 1 | CTD_human |
Tgene | RYR2 | C1510586 | Autism Spectrum Disorders | 1 | CTD_human |