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Fusion Protein:CBFB-PLEKHG4 |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: CBFB-PLEKHG4 | FusionPDB ID: 13376 | FusionGDB2.0 ID: 13376 | Hgene | Tgene | Gene symbol | CBFB | PLEKHG4 | Gene ID | 865 | 25894 |
| Gene name | core-binding factor subunit beta | pleckstrin homology and RhoGEF domain containing G4 | |
| Synonyms | PEBP2B | ARHGEF44|PRTPHN1|SCA4 | |
| Cytomap | 16q22.1 | 16q22.1 | |
| Type of gene | protein-coding | protein-coding | |
| Description | core-binding factor subunit betaCBF-betaPEA2-betaPEBP2-betaSL3-3 enhancer factor 1 beta subunitSL3-3 enhancer factor 1 subunit betaSL3/AKV core-binding factor beta subunitcore-binding factor beta subunitpolyomavirus enhancer binding protein 2, bet | puratrophin-1PH domain-containing family G member 4Purkinje cell atrophy associated protein 1pleckstrin homology domain containing, family G (with RhoGef domain) member 4 | |
| Modification date | 20200320 | 20200313 | |
| UniProtAcc | Q13951 | . | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000290858, ENST00000412916, ENST00000561924, ENST00000568858, | ENST00000360461, ENST00000379344, ENST00000427155, ENST00000450733, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 17 X 18 X 12=3672 | 2 X 4 X 2=16 |
| # samples | 33 | 2 | |
| ** MAII score | log2(33/3672*10)=-3.47602812916799 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(2/16*10)=0.321928094887362 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
| Context (manual curation of fusion genes in FusionPDB) | PubMed: CBFB [Title/Abstract] AND PLEKHG4 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | CBFB(67116211)-PLEKHG4(67312644), # samples:2 | ||
| Anticipated loss of major functional domain due to fusion event. | CBFB-PLEKHG4 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. CBFB-PLEKHG4 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. CBFB-PLEKHG4 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF. CBFB-PLEKHG4 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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 |
| Fusion gene breakpoints across CBFB (5'-gene) * 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 breakpoints across PLEKHG4 (3'-gene) * 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 |
| Fusion gene information from FusionGDB2.0. |
| 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 | OV | TCGA-13-1407-01A | CBFB | chr16 | 67116211 | + | PLEKHG4 | chr16 | 67311680 | + |
| ChimerDB4 | OV | TCGA-13-1407-01A | CBFB | chr16 | 67116211 | + | PLEKHG4 | chr16 | 67312644 | + |
| ChimerDB4 | OV | TCGA-13-1407-01A | CBFB | chr16 | 67116211 | + | PLEKHG4 | chr16 | 67314028 | + |
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Fusion ORF Analysis |
| Fusion information from ORFfinder translation from full-length transcript sequence from FusionPDB. |
| 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) |
| ENST00000412916 | CBFB | chr16 | 67116211 | + | ENST00000360461 | PLEKHG4 | chr16 | 67314028 | + | 4824 | 658 | 163 | 4152 | 1329 |
| ENST00000412916 | CBFB | chr16 | 67116211 | + | ENST00000450733 | PLEKHG4 | chr16 | 67314028 | + | 4601 | 658 | 163 | 3909 | 1248 |
| 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 |
| ENST00000412916 | ENST00000360461 | CBFB | chr16 | 67116211 | + | PLEKHG4 | chr16 | 67314028 | + | 0.005288378 | 0.99471164 |
| ENST00000412916 | ENST00000450733 | CBFB | chr16 | 67116211 | + | PLEKHG4 | chr16 | 67314028 | + | 0.005479475 | 0.99452055 |
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Fusion Amino Acid Sequences |
| For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
| >FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >13376_13376_1_CBFB-PLEKHG4_CBFB_chr16_67116211_ENST00000412916_PLEKHG4_chr16_67314028_ENST00000360461_length(amino acids)=1329AA_BP=0 MPRVVPDQRSKFENEEFFRKLSRECEIKYTGFRDRPHEERQARFQNACRDGRSEIAFVATGTNLSLQFFPASWQGEQRQTPSREYVDLER EAGKVYLKAPMILNGVCVIWKGWIDLQRLDGMGCLEFDEERAQQEDALAQQAFEEARRRTREFEDRDRSHREEMEFRDAWEEEEPASQMH VKDPGPPRPPAGATQDEELQGSPLSRKFQLPPAADESGDAQRGTVESSSVLSEGPGPSGVESLLCPMSSHLSLAQGESDTPGVGLVGDPG PSRAMPSGLSPGALDSDPVGLGDPLSEISKLLEAAPSGSGLPKPADCLLAQDLCWELLASGMATLPGTRDVQGRAVLLLCAHSPAWLQSE CSSQELIRLLLYLRSIPRPEVQALGLTVLVDARICAPSSSLFSGLSQLQEAAPGAVYQVLLVGSTLLKEVPSGLQLEQLPSQSLLTHIPT AGLPTSLGGGLPYCHQAWLDFRRRLEALLQNCQAACALLQGAIESVKAVPQPMEPGEVGQLLQQTEVLMQQVLDSPWLAWLQCQGGRELT WLKQEVPEVTLSPDYRTAMDKADELYDRVDGLLHQLTLQSNQRIQALELVQTLEARESGLHQIEVWLQQVGWPALEEAGEPSLDMLLQAQ GSFQELYQVAQEQVRQGEKFLQPLTGWEAAELDPPGARFLALRAQLTEFSRALAQRCQRLADAERLFQLFREALTWAEEGQRVLAELEQE RPGVVLQQLQLHWTRHPDLPPAHFRKMWALATGLGSEAIRQECRWAWARCQDTWLALDQKLEASLKLPPVGSTASLCVSQVPAAPAHPPL RKAYSFDRNLGQSLSEPACHCHHAATIAACRRPEAGGGALPQASPTVPPPGSSDPRSLNRLQLVLAEMVATEREYVRALEYTMENYFPEL DRPDVPQGLRGQRAHLFGNLEKLRDFHCHFFLRELEACTRHPPRVAYAFLRHRVQFGMYALYSKNKPRSDALMSSYGHTFFKDKQQALGD HLDLASYLLKPIQRMGKYALLLQELARACGGPTQELSALREAQSLVHFQLRHGNDLLAMDAIQGCDVNLKEQGQLVRQDEFVVRTGRHKS VRRIFLFEELLLFSKPRHGPTGVDTFAYKRSFKMADLGLTECCGNSNLRFEIWFRRRKARDTFVLQASSLAIKQAWTADISHLLWRQAVH NKEVRMAEMVSMGVGNKAFRDIAPSEEAINDRTVNYVLKCREVRSRASIAVAPFDHDSLYLGASNSLPGDPASCSVLGSLNLHLYRDPAL -------------------------------------------------------------- >13376_13376_2_CBFB-PLEKHG4_CBFB_chr16_67116211_ENST00000412916_PLEKHG4_chr16_67314028_ENST00000450733_length(amino acids)=1248AA_BP=0 MPRVVPDQRSKFENEEFFRKLSRECEIKYTGFRDRPHEERQARFQNACRDGRSEIAFVATGTNLSLQFFPASWQGEQRQTPSREYVDLER EAGKVYLKAPMILNGVCVIWKGWIDLQRLDGMGCLEFDEERAQQEDALAQQAFEEARRRTREFEDRDRSHREEMEFRDAWEEEEPASQMH VKDPGPPRPPAGATQDEELQGSPLSRKFQLPPAADESGDAQRGTVESSSVLSEGPGPSGVESLLCPMSSHLSLAQGTRDVQGRAVLLLCA HSPAWLQSECSSQELIRLLLYLRSIPRPEVQALGLTVLVDARICAPSSSLFSGLSQLQEAAPGAVYQVLLVGSTLLKEVPSGLQLEQLPS QSLLTHIPTAGLPTSLGGGLPYCHQAWLDFRRRLEALLQNCQAACALLQGAIESVKAVPQPMEPGEVGQLLQQTEVLMQQVLDSPWLAWL QCQGGRELTWLKQEVPEVTLSPDYRTAMDKADELYDRVDGLLHQLTLQSNQRIQALELVQTLEARESGLHQIEVWLQQVGWPALEEAGEP SLDMLLQAQGSFQELYQVAQEQVRQGEKFLQPLTGWEAAELDPPGARFLALRAQLTEFSRALAQRCQRLADAERLFQLFREALTWAEEGQ RVLAELEQERPGVVLQQLQLHWTRHPDLPPAHFRKMWALATGLGSEAIRQECRWAWARCQDTWLALDQKLEASLKLPPVGSTASLCVSQV PAAPAHPPLRKAYSFDRNLGQSLSEPACHCHHAATIAACRRPEAGGGALPQASPTVPPPGSSDPRSLNRLQLVLAEMVATEREYVRALEY TMENYFPELDRPDVPQGLRGQRAHLFGNLEKLRDFHCHFFLRELEACTRHPPRVAYAFLRHRVQFGMYALYSKNKPRSDALMSSYGHTFF KDKQQALGDHLDLASYLLKPIQRMGKYALLLQELARACGGPTQELSALREAQSLVHFQLRHGNDLLAMDAIQGCDVNLKEQGQLVRQDEF VVRTGRHKSVRRIFLFEELLLFSKPRHGPTGVDTFAYKRSFKMADLGLTECCGNSNLRFEIWFRRRKARDTFVLQASSLAIKQAWTADIS HLLWRQAVHNKEVRMAEMVSMGVGNKAFRDIAPSEEAINDRTVNYVLKCREVRSRASIAVAPFDHDSLYLGASNSLPGDPASCSVLGSLN -------------------------------------------------------------- |
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Fusion Protein Functional Features |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr16:67116211/chr16:67312644) - 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 |
| CBFB | . |
| FUNCTION: Forms the heterodimeric complex core-binding factor (CBF) with RUNX family proteins (RUNX1, RUNX2, and RUNX3). 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. 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. {ECO:0000250|UniProtKB:Q08024}. | 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. |
| - 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 |
| Tgene | PLEKHG4 | chr16:67116211 | chr16:67314028 | ENST00000360461 | 0 | 21 | 732_908 | 0 | 1192.0 | Domain | DH | |
| Tgene | PLEKHG4 | chr16:67116211 | chr16:67314028 | ENST00000360461 | 0 | 21 | 920_1027 | 0 | 1192.0 | Domain | PH | |
| Tgene | PLEKHG4 | chr16:67116211 | chr16:67314028 | ENST00000379344 | 0 | 22 | 732_908 | 0 | 1192.0 | Domain | DH | |
| Tgene | PLEKHG4 | chr16:67116211 | chr16:67314028 | ENST00000379344 | 0 | 22 | 920_1027 | 0 | 1192.0 | Domain | PH | |
| Tgene | PLEKHG4 | chr16:67116211 | chr16:67314028 | ENST00000427155 | 0 | 22 | 732_908 | 0 | 1192.0 | Domain | DH | |
| Tgene | PLEKHG4 | chr16:67116211 | chr16:67314028 | ENST00000427155 | 0 | 22 | 920_1027 | 0 | 1192.0 | Domain | PH | |
| Tgene | PLEKHG4 | chr16:67116211 | chr16:67314028 | ENST00000450733 | 0 | 20 | 732_908 | 0 | 1111.0 | Domain | DH | |
| Tgene | PLEKHG4 | chr16:67116211 | chr16:67314028 | ENST00000450733 | 0 | 20 | 920_1027 | 0 | 1111.0 | Domain | PH |
| - 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 Protein-Protein Interaction |
| 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 from validated records (BIOGRID-3.4.160) |
| Gene | PPI interactors |
| CBFB | CHGB, RUNX1, MYOD1, RUNX3, COPRS, KMT2A, ELAVL1, CUL5, vif, nef, APOBEC3G, MYC, RAB2A, TCEB1, RNF7, TCEB2, RUNX2, ARL6IP6, SERPINB5, SLC25A32, TAS2R41, CRIP1, GALK1, PPIA, SOD1, NFATC1, GCHFR, G3BP1, CTNNB1, CBFA2T3, NKX2-1, IKZF3, IKZF1, AMBRA1, TRIM28, BAG3, BCL11B, CBFB, EMD, ETS1, HAX1, HLTF, HNRNPM, HSPBP1, PML, RBM14, TCF12, TCF7, TSC2, TUBA4A, ZBTB1, AKAP8L, ANXA1, HDAC3, IKZF2, SEC16A, TAF4, PDCD6IP, ARIH1, ARIH2, CUL2, DCAF11, NCOR1, NEDD8, RBX1, YTHDF2, PLEKHA4, CHRM5, BRD4, DDX58, ATG7, FBXW12, NIP7, HSPA1A, FCN3, FAM109A, LHFPL4, FOXF2, LRRC32, DUOXA2, VPS28, SMPDL3B, RP2, AQP12B, BTF3, |
| Protein-protein interactors based on sequence similarity (STRING) |
| Gene | STRING network |
| CBFB |  |
| PLEKHG4 |
| - Retained interactions in fusion protein (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost interactions due to fusion (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs to CBFB-PLEKHG4 |
| Drugs used for this fusion-positive patient. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to CBFB-PLEKHG4 |
| Diseases that have this fusion gene. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Disease | Source | PMID |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | CBFB | C0023467 | Leukemia, Myelocytic, Acute | 2 | CTD_human |
| Hgene | CBFB | C0023479 | Acute myelomonocytic leukemia | 2 | CTD_human;ORPHANET |
| Hgene | CBFB | C0026998 | Acute Myeloid Leukemia, M1 | 2 | CTD_human |
| Hgene | CBFB | C1879321 | Acute Myeloid Leukemia (AML-M2) | 2 | CTD_human |
| Hgene | CBFB | C0005941 | Bone Diseases, Developmental | 1 | CTD_human |
| Hgene | CBFB | C0008925 | Cleft Palate | 1 | CTD_human |
| Hgene | CBFB | C0018798 | Congenital Heart Defects | 1 | CTD_human |
| Hgene | CBFB | C0029396 | Heterotopic Ossification | 1 | CTD_human |
| Hgene | CBFB | C1837218 | Cleft palate, isolated | 1 | CTD_human |
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