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Fusion Protein:RARB-FAM19A4 |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: RARB-FAM19A4 | FusionPDB ID: 72331 | FusionGDB2.0 ID: 72331 | Hgene | Tgene | Gene symbol | RARB | FAM19A4 | Gene ID | 5915 | 151647 |
Gene name | retinoic acid receptor beta | TAFA chemokine like family member 4 | |
Synonyms | HAP|MCOPS12|NR1B2|RARbeta1|RRB2 | FAM19A4|TAFA-4 | |
Cytomap | 3p24.2 | 3p14.1 | |
Type of gene | protein-coding | protein-coding | |
Description | retinoic acid receptor betaHBV-activated proteinRAR-betaRAR-epsilonhepatitis B virus activated proteinnuclear receptor subfamily 1 group B member 2retinoic acid receptor, beta polypeptide | chemokine-like protein TAFA-4family with sequence similarity 19 (chemokine (C-C motif)-like), member A4family with sequence similarity 19 member A4, C-C motif chemokine likeprotein FAM19A4 | |
Modification date | 20200328 | 20200313 | |
UniProtAcc | . | . | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000462272, ENST00000330688, ENST00000404969, ENST00000437042, ENST00000458646, | ENST00000295569, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 12 X 11 X 5=660 | 4 X 5 X 4=80 |
# samples | 12 | 4 | |
** MAII score | log2(12/660*10)=-2.4594316186373 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(4/80*10)=-1 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: RARB [Title/Abstract] AND FAM19A4 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | RARB(25542814)-FAM19A4(68802169), # samples:2 | ||
Anticipated loss of major functional domain due to fusion event. | RARB-FAM19A4 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. RARB-FAM19A4 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. RARB-FAM19A4 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. RARB-FAM19A4 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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * 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 Sample Information |
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![]() * 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 | PRAD | TCGA-EJ-5501-01A | RARB | chr3 | 25542814 | - | FAM19A4 | chr3 | 68802169 | - |
ChimerDB4 | PRAD | TCGA-EJ-5501-01A | RARB | chr3 | 25542814 | + | FAM19A4 | chr3 | 68802169 | - |
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Fusion ORF Analysis |
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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) |
ENST00000404969 | RARB | chr3 | 25542814 | + | ENST00000295569 | FAM19A4 | chr3 | 68802169 | - | 2138 | 469 | 0 | 761 | 253 |
ENST00000437042 | RARB | chr3 | 25542814 | + | ENST00000295569 | FAM19A4 | chr3 | 68802169 | - | 2229 | 560 | 97 | 852 | 251 |
ENST00000330688 | RARB | chr3 | 25542814 | + | ENST00000295569 | FAM19A4 | chr3 | 68802169 | - | 2538 | 869 | 394 | 1161 | 255 |
ENST00000458646 | RARB | chr3 | 25542814 | + | ENST00000295569 | FAM19A4 | chr3 | 68802169 | - | 2044 | 375 | 65 | 667 | 200 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000404969 | ENST00000295569 | RARB | chr3 | 25542814 | + | FAM19A4 | chr3 | 68802169 | - | 0.002489279 | 0.9975107 |
ENST00000437042 | ENST00000295569 | RARB | chr3 | 25542814 | + | FAM19A4 | chr3 | 68802169 | - | 0.009535982 | 0.990464 |
ENST00000330688 | ENST00000295569 | RARB | chr3 | 25542814 | + | FAM19A4 | chr3 | 68802169 | - | 0.001760516 | 0.9982395 |
ENST00000458646 | ENST00000295569 | RARB | chr3 | 25542814 | + | FAM19A4 | chr3 | 68802169 | - | 0.02318759 | 0.9768124 |
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Fusion Amino Acid Sequences |
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>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >72331_72331_1_RARB-FAM19A4_RARB_chr3_25542814_ENST00000330688_FAM19A4_chr3_68802169_ENST00000295569_length(amino acids)=255AA_BP=159 MQTFSAREIMFDCMDVLSVSPGQILDFYTASPSSCMLQEKALKACFSGLTQTEWQHRHTAQSIETQSTSSEELVPSPPSPLPPPRVYKPC FVCQDKSSGYHYGVSACEGCKGFFRRSIQKNMIYTCHRDKNCVINKVTRNRCQYCRLQKCFEVGMSKECHHQIKQGTCEVVAVHRCCNKN -------------------------------------------------------------- >72331_72331_2_RARB-FAM19A4_RARB_chr3_25542814_ENST00000404969_FAM19A4_chr3_68802169_ENST00000295569_length(amino acids)=253AA_BP=157 MTTSGHACPVPAVNGHMTHYPATPYPLLFPPVIGGLSLPPLHGLHGHPPPSGCSTPSPATIETQSTSSEELVPSPPSPLPPPRVYKPCFV CQDKSSGYHYGVSACEGCKGFFRRSIQKNMIYTCHRDKNCVINKVTRNRCQYCRLQKCFEVGMSKECHHQIKQGTCEVVAVHRCCNKNRI -------------------------------------------------------------- >72331_72331_3_RARB-FAM19A4_RARB_chr3_25542814_ENST00000437042_FAM19A4_chr3_68802169_ENST00000295569_length(amino acids)=251AA_BP=155 MGCRERERSEQGLSGHRRGRIRNAFGRLFASIYLEGELGIFLGTPRPGWIGRASLENAIETQSTSSEELVPSPPSPLPPPRVYKPCFVCQ DKSSGYHYGVSACEGCKGFFRRSIQKNMIYTCHRDKNCVINKVTRNRCQYCRLQKCFEVGMSKECHHQIKQGTCEVVAVHRCCNKNRIEE -------------------------------------------------------------- >72331_72331_4_RARB-FAM19A4_RARB_chr3_25542814_ENST00000458646_FAM19A4_chr3_68802169_ENST00000295569_length(amino acids)=200AA_BP=104 MSEKIVAIETQSTSSEELVPSPPSPLPPPRVYKPCFVCQDKSSGYHYGVSACEGCKGFFRRSIQKNMIYTCHRDKNCVINKVTRNRCQYC RLQKCFEVGMSKECHHQIKQGTCEVVAVHRCCNKNRIEERSQTVKCSCFPGQVAGTTRAQPSCVEASIVIQKWWCHMNPCLEGEDCKVLP -------------------------------------------------------------- |
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Fusion Protein Functional Features |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr3:25542814/chr3:68802169) - 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 |
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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. | 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. |
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- 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 |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000404969 | + | 3 | 8 | 88_153 | 156.33333333333334 | 456.0 | DNA binding | Nuclear receptor |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000330688 | + | 3 | 8 | 1_87 | 149.33333333333334 | 449.0 | Region | Note=Modulating |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000404969 | + | 3 | 8 | 1_87 | 156.33333333333334 | 456.0 | Region | Note=Modulating |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000330688 | + | 3 | 8 | 124_148 | 149.33333333333334 | 449.0 | Zinc finger | NR C4-type |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000330688 | + | 3 | 8 | 88_108 | 149.33333333333334 | 449.0 | Zinc finger | NR C4-type |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000404969 | + | 3 | 8 | 124_148 | 156.33333333333334 | 456.0 | Zinc finger | NR C4-type |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000404969 | + | 3 | 8 | 88_108 | 156.33333333333334 | 456.0 | Zinc finger | NR C4-type |
- 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 |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000330688 | + | 3 | 8 | 88_153 | 149.33333333333334 | 449.0 | DNA binding | Nuclear receptor |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000437042 | + | 3 | 8 | 88_153 | 37.333333333333336 | 337.0 | DNA binding | Nuclear receptor |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000458646 | + | 3 | 8 | 88_153 | 37.333333333333336 | 337.0 | DNA binding | Nuclear receptor |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000330688 | + | 3 | 8 | 183_417 | 149.33333333333334 | 449.0 | Domain | NR LBD |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000404969 | + | 3 | 8 | 183_417 | 156.33333333333334 | 456.0 | Domain | NR LBD |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000437042 | + | 3 | 8 | 183_417 | 37.333333333333336 | 337.0 | Domain | NR LBD |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000458646 | + | 3 | 8 | 183_417 | 37.333333333333336 | 337.0 | Domain | NR LBD |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000330688 | + | 3 | 8 | 154_182 | 149.33333333333334 | 449.0 | Region | Note=Hinge |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000404969 | + | 3 | 8 | 154_182 | 156.33333333333334 | 456.0 | Region | Note=Hinge |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000437042 | + | 3 | 8 | 154_182 | 37.333333333333336 | 337.0 | Region | Note=Hinge |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000437042 | + | 3 | 8 | 1_87 | 37.333333333333336 | 337.0 | Region | Note=Modulating |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000458646 | + | 3 | 8 | 154_182 | 37.333333333333336 | 337.0 | Region | Note=Hinge |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000458646 | + | 3 | 8 | 1_87 | 37.333333333333336 | 337.0 | Region | Note=Modulating |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000437042 | + | 3 | 8 | 124_148 | 37.333333333333336 | 337.0 | Zinc finger | NR C4-type |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000437042 | + | 3 | 8 | 88_108 | 37.333333333333336 | 337.0 | Zinc finger | NR C4-type |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000458646 | + | 3 | 8 | 124_148 | 37.333333333333336 | 337.0 | Zinc finger | NR C4-type |
Hgene | RARB | chr3:25542814 | chr3:68802169 | ENST00000458646 | + | 3 | 8 | 88_108 | 37.333333333333336 | 337.0 | Zinc finger | NR C4-type |
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Fusion Protein-Protein Interaction |
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Gene | PPI interactors |
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Gene | STRING network |
RARB | |
FAM19A4 |
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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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Related Drugs to RARB-FAM19A4 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to RARB-FAM19A4 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |