|
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:BAZ1B-BAZ1B (FusionGDB2 ID:9096) |
Fusion Gene Summary for BAZ1B-BAZ1B |
Fusion gene summary |
Fusion gene information | Fusion gene name: BAZ1B-BAZ1B | Fusion gene ID: 9096 | Hgene | Tgene | Gene symbol | BAZ1B | BAZ1B | Gene ID | 9031 | 9031 |
Gene name | bromodomain adjacent to zinc finger domain 1B | bromodomain adjacent to zinc finger domain 1B | |
Synonyms | WBSCR10|WBSCR9|WSTF | WBSCR10|WBSCR9|WSTF | |
Cytomap | 7q11.23 | 7q11.23 | |
Type of gene | protein-coding | protein-coding | |
Description | tyrosine-protein kinase BAZ1BhWALp2transcription factor WSTFwilliams syndrome transcription factorwilliams-Beuren syndrome chromosomal region 10 proteinwilliams-Beuren syndrome chromosomal region 9 protein | tyrosine-protein kinase BAZ1BhWALp2transcription factor WSTFwilliams syndrome transcription factorwilliams-Beuren syndrome chromosomal region 10 proteinwilliams-Beuren syndrome chromosomal region 9 protein | |
Modification date | 20200313 | 20200313 | |
UniProtAcc | Q9UIG0 | Q9UIG0 | |
Ensembl transtripts involved in fusion gene | ENST00000339594, ENST00000404251, | ENST00000339594, ENST00000404251, | |
Fusion gene scores | * DoF score | 14 X 17 X 6=1428 | 10 X 11 X 5=550 |
# samples | 20 | 13 | |
** MAII score | log2(20/1428*10)=-2.83592407425437 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(13/550*10)=-2.08091999538357 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: BAZ1B [Title/Abstract] AND BAZ1B [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | BAZ1B(72855211)-BAZ1B(72855230), # samples:1 BAZ1B(72856520)-BAZ1B(72855901), # samples:1 BAZ1B(72891983)-BAZ1B(72891837), # samples:1 BAZ1B(72891980)-BAZ1B(72891827), # 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) |
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 |
Hgene | BAZ1B | GO:0006974 | cellular response to DNA damage stimulus | 19092802 |
Hgene | BAZ1B | GO:0016572 | histone phosphorylation | 19092802 |
Tgene | BAZ1B | GO:0006974 | cellular response to DNA damage stimulus | 19092802 |
Tgene | BAZ1B | GO:0016572 | histone phosphorylation | 19092802 |
Fusion gene breakpoints across BAZ1B (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 BAZ1B (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 |
ChiTaRS5.0 | N/A | AA230242 | BAZ1B | chr7 | 72855211 | - | BAZ1B | chr7 | 72855230 | + |
ChiTaRS5.0 | N/A | AB032253 | BAZ1B | chr7 | 72856520 | - | BAZ1B | chr7 | 72855901 | + |
ChiTaRS5.0 | N/A | BE813822 | BAZ1B | chr7 | 72891983 | + | BAZ1B | chr7 | 72891837 | - |
ChiTaRS5.0 | N/A | BF326857 | BAZ1B | chr7 | 72891980 | + | BAZ1B | chr7 | 72891827 | - |
Top |
Fusion Gene ORF analysis for BAZ1B-BAZ1B |
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 |
intron-3UTR | ENST00000339594 | ENST00000339594 | BAZ1B | chr7 | 72855211 | - | BAZ1B | chr7 | 72855230 | + |
intron-intron | ENST00000339594 | ENST00000404251 | BAZ1B | chr7 | 72855211 | - | BAZ1B | chr7 | 72855230 | + |
intron-3UTR | ENST00000404251 | ENST00000339594 | BAZ1B | chr7 | 72855211 | - | BAZ1B | chr7 | 72855230 | + |
intron-intron | ENST00000404251 | ENST00000404251 | BAZ1B | chr7 | 72855211 | - | BAZ1B | chr7 | 72855230 | + |
intron-3UTR | ENST00000339594 | ENST00000339594 | BAZ1B | chr7 | 72856520 | - | BAZ1B | chr7 | 72855901 | + |
intron-3UTR | ENST00000339594 | ENST00000404251 | BAZ1B | chr7 | 72856520 | - | BAZ1B | chr7 | 72855901 | + |
intron-3UTR | ENST00000404251 | ENST00000339594 | BAZ1B | chr7 | 72856520 | - | BAZ1B | chr7 | 72855901 | + |
intron-3UTR | ENST00000404251 | ENST00000404251 | BAZ1B | chr7 | 72856520 | - | BAZ1B | chr7 | 72855901 | + |
intron-3CDS | ENST00000339594 | ENST00000339594 | BAZ1B | chr7 | 72891983 | + | BAZ1B | chr7 | 72891837 | - |
intron-3CDS | ENST00000339594 | ENST00000404251 | BAZ1B | chr7 | 72891983 | + | BAZ1B | chr7 | 72891837 | - |
intron-3CDS | ENST00000404251 | ENST00000339594 | BAZ1B | chr7 | 72891983 | + | BAZ1B | chr7 | 72891837 | - |
intron-3CDS | ENST00000404251 | ENST00000404251 | BAZ1B | chr7 | 72891983 | + | BAZ1B | chr7 | 72891837 | - |
intron-3CDS | ENST00000339594 | ENST00000339594 | BAZ1B | chr7 | 72891980 | + | BAZ1B | chr7 | 72891827 | - |
intron-3CDS | ENST00000339594 | ENST00000404251 | BAZ1B | chr7 | 72891980 | + | BAZ1B | chr7 | 72891827 | - |
intron-3CDS | ENST00000404251 | ENST00000339594 | BAZ1B | chr7 | 72891980 | + | BAZ1B | chr7 | 72891827 | - |
intron-3CDS | ENST00000404251 | ENST00000404251 | BAZ1B | chr7 | 72891980 | + | BAZ1B | chr7 | 72891827 | - |
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 |
Top |
Fusion Genomic Features for BAZ1B-BAZ1B |
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. |
Top |
Fusion Protein Features for BAZ1B-BAZ1B |
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. |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
BAZ1B | BAZ1B |
FUNCTION: Atypical tyrosine-protein kinase that plays a central role in chromatin remodeling and acts as a transcription regulator. Involved in DNA damage response by phosphorylating 'Tyr-142' of histone H2AX (H2AXY142ph). H2AXY142ph plays a central role in DNA repair and acts as a mark that distinguishes between apoptotic and repair responses to genotoxic stress. Essential component of the WICH complex, a chromatin remodeling complex that mobilizes nucleosomes and reconfigures irregular chromatin to a regular nucleosomal array structure. The WICH complex regulates the transcription of various genes, has a role in RNA polymerase I and RNA polymerase III transcription, mediates the histone H2AX phosphorylation at 'Tyr-142', and is involved in the maintenance of chromatin structures during DNA replication processes. In the complex, it mediates the recruitment of the WICH complex to replication foci during DNA replication. {ECO:0000269|PubMed:11980720, ECO:0000269|PubMed:15543136, ECO:0000269|PubMed:16603771, ECO:0000269|PubMed:19092802, ECO:0000269|PubMed:19234442}. | FUNCTION: Atypical tyrosine-protein kinase that plays a central role in chromatin remodeling and acts as a transcription regulator. Involved in DNA damage response by phosphorylating 'Tyr-142' of histone H2AX (H2AXY142ph). H2AXY142ph plays a central role in DNA repair and acts as a mark that distinguishes between apoptotic and repair responses to genotoxic stress. Essential component of the WICH complex, a chromatin remodeling complex that mobilizes nucleosomes and reconfigures irregular chromatin to a regular nucleosomal array structure. The WICH complex regulates the transcription of various genes, has a role in RNA polymerase I and RNA polymerase III transcription, mediates the histone H2AX phosphorylation at 'Tyr-142', and is involved in the maintenance of chromatin structures during DNA replication processes. In the complex, it mediates the recruitment of the WICH complex to replication foci during DNA replication. {ECO:0000269|PubMed:11980720, ECO:0000269|PubMed:15543136, ECO:0000269|PubMed:16603771, ECO:0000269|PubMed:19092802, ECO:0000269|PubMed:19234442}. |
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 |
Top |
Fusion Gene Sequence for BAZ1B-BAZ1B |
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. |
Top |
Fusion Gene PPI Analysis for BAZ1B-BAZ1B |
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 |
Top |
Related Drugs for BAZ1B-BAZ1B |
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 |
Top |
Related Diseases for BAZ1B-BAZ1B |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | BAZ1B | C0175702 | Williams Syndrome | 1 | CTD_human |
Tgene | BAZ1B | C0175702 | Williams Syndrome | 1 | CTD_human |