![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: BAZ1B |
Gene summary for BAZ1B |
![]() |
Gene information | Species | Human | Gene symbol | BAZ1B | Gene ID | 9031 |
Gene name | bromodomain adjacent to zinc finger domain 1B | |
Gene Alias | WBSCR10 | |
Cytomap | 7q11.23 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q9UIG0 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
9031 | BAZ1B | LZE2T | Human | Esophagus | ESCC | 4.47e-05 | 6.80e-01 | 0.082 |
9031 | BAZ1B | LZE4T | Human | Esophagus | ESCC | 3.21e-12 | 3.28e-01 | 0.0811 |
9031 | BAZ1B | LZE7T | Human | Esophagus | ESCC | 1.15e-07 | 6.49e-01 | 0.0667 |
9031 | BAZ1B | LZE8T | Human | Esophagus | ESCC | 6.54e-05 | 1.38e-01 | 0.067 |
9031 | BAZ1B | LZE20T | Human | Esophagus | ESCC | 3.36e-04 | 2.43e-01 | 0.0662 |
9031 | BAZ1B | LZE22T | Human | Esophagus | ESCC | 2.31e-08 | 4.93e-01 | 0.068 |
9031 | BAZ1B | LZE24T | Human | Esophagus | ESCC | 1.73e-25 | 5.76e-01 | 0.0596 |
9031 | BAZ1B | LZE6T | Human | Esophagus | ESCC | 2.59e-03 | 2.03e-01 | 0.0845 |
9031 | BAZ1B | P1T-E | Human | Esophagus | ESCC | 2.74e-16 | 8.74e-01 | 0.0875 |
9031 | BAZ1B | P2T-E | Human | Esophagus | ESCC | 7.37e-49 | 9.54e-01 | 0.1177 |
9031 | BAZ1B | P4T-E | Human | Esophagus | ESCC | 1.43e-35 | 1.04e+00 | 0.1323 |
9031 | BAZ1B | P5T-E | Human | Esophagus | ESCC | 8.17e-28 | 6.70e-01 | 0.1327 |
9031 | BAZ1B | P8T-E | Human | Esophagus | ESCC | 2.58e-32 | 4.83e-01 | 0.0889 |
9031 | BAZ1B | P9T-E | Human | Esophagus | ESCC | 5.94e-23 | 5.46e-01 | 0.1131 |
9031 | BAZ1B | P10T-E | Human | Esophagus | ESCC | 1.17e-51 | 9.34e-01 | 0.116 |
9031 | BAZ1B | P11T-E | Human | Esophagus | ESCC | 2.60e-15 | 7.83e-01 | 0.1426 |
9031 | BAZ1B | P12T-E | Human | Esophagus | ESCC | 3.16e-56 | 1.07e+00 | 0.1122 |
9031 | BAZ1B | P15T-E | Human | Esophagus | ESCC | 9.59e-43 | 9.89e-01 | 0.1149 |
9031 | BAZ1B | P16T-E | Human | Esophagus | ESCC | 6.05e-56 | 1.15e+00 | 0.1153 |
9031 | BAZ1B | P17T-E | Human | Esophagus | ESCC | 1.15e-11 | 6.65e-01 | 0.1278 |
Page: 1 2 3 4 5 6 7 |
![]() |
∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage. |
Top |
Malignant transformation related pathway analysis |
![]() |
![]() |
Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | AD | ![]() |
Colorectum | SER | ![]() |
Colorectum | MSS | ![]() |
Colorectum | MSI-H | ![]() |
Colorectum | FAP | ![]() |
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust). |
Page: 1 2 3 4 5 6 7 8 9 |
![]() |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:001657015 | Esophagus | ESCC | histone modification | 323/8552 | 463/18723 | 2.61e-26 | 7.88e-24 | 323 |
GO:000632517 | Esophagus | ESCC | chromatin organization | 240/8552 | 409/18723 | 6.52e-08 | 1.14e-06 | 240 |
GO:00182124 | Esophagus | ESCC | peptidyl-tyrosine modification | 202/8552 | 378/18723 | 1.34e-03 | 6.39e-03 | 202 |
GO:00181084 | Esophagus | ESCC | peptidyl-tyrosine phosphorylation | 200/8552 | 375/18723 | 1.60e-03 | 7.45e-03 | 200 |
GO:00165721 | Esophagus | ESCC | histone phosphorylation | 27/8552 | 39/18723 | 2.52e-03 | 1.08e-02 | 27 |
GO:001657011 | Liver | Cirrhotic | histone modification | 154/4634 | 463/18723 | 1.92e-05 | 2.57e-04 | 154 |
GO:001657021 | Liver | HCC | histone modification | 283/7958 | 463/18723 | 2.68e-16 | 2.33e-14 | 283 |
GO:000632511 | Liver | HCC | chromatin organization | 206/7958 | 409/18723 | 7.23e-04 | 4.41e-03 | 206 |
GO:00165707 | Oral cavity | OSCC | histone modification | 270/7305 | 463/18723 | 1.59e-17 | 1.50e-15 | 270 |
GO:00182123 | Oral cavity | OSCC | peptidyl-tyrosine modification | 180/7305 | 378/18723 | 3.63e-04 | 2.22e-03 | 180 |
GO:00181083 | Oral cavity | OSCC | peptidyl-tyrosine phosphorylation | 177/7305 | 375/18723 | 6.86e-04 | 3.83e-03 | 177 |
GO:000632510 | Oral cavity | OSCC | chromatin organization | 190/7305 | 409/18723 | 1.17e-03 | 5.97e-03 | 190 |
GO:0016572 | Oral cavity | OSCC | histone phosphorylation | 24/7305 | 39/18723 | 3.64e-03 | 1.51e-02 | 24 |
GO:001657023 | Oral cavity | EOLP | histone modification | 98/2218 | 463/18723 | 5.58e-09 | 2.96e-07 | 98 |
GO:000632515 | Oral cavity | EOLP | chromatin organization | 84/2218 | 409/18723 | 2.68e-07 | 8.16e-06 | 84 |
GO:00182121 | Oral cavity | EOLP | peptidyl-tyrosine modification | 65/2218 | 378/18723 | 1.25e-03 | 9.02e-03 | 65 |
GO:00181081 | Oral cavity | EOLP | peptidyl-tyrosine phosphorylation | 64/2218 | 375/18723 | 1.65e-03 | 1.09e-02 | 64 |
GO:00063383 | Oral cavity | EOLP | chromatin remodeling | 46/2218 | 255/18723 | 2.34e-03 | 1.44e-02 | 46 |
GO:001657031 | Oral cavity | NEOLP | histone modification | 88/2005 | 463/18723 | 5.59e-08 | 2.23e-06 | 88 |
GO:000632521 | Oral cavity | NEOLP | chromatin organization | 70/2005 | 409/18723 | 4.97e-05 | 6.83e-04 | 70 |
Page: 1 2 3 |
![]() |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
Page: 1 |
Top |
Cell-cell communication analysis |
![]() |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
Top |
Single-cell gene regulatory network inference analysis |
![]() |
TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression. |
Page: 1 |
Top |
Somatic mutation of malignant transformation related genes |
![]() |
Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
BAZ1B | SNV | Missense_Mutation | novel | c.3566N>G | p.Val1189Gly | p.V1189G | Q9UIG0 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-5L-AAT0-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD |
BAZ1B | SNV | Missense_Mutation | c.3100N>G | p.Leu1034Val | p.L1034V | Q9UIG0 | protein_coding | tolerated(0.19) | probably_damaging(0.991) | TCGA-A1-A0SI-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
BAZ1B | SNV | Missense_Mutation | rs782432522 | c.1270C>T | p.Pro424Ser | p.P424S | Q9UIG0 | protein_coding | tolerated(0.34) | benign(0.031) | TCGA-A2-A0CX-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD |
BAZ1B | SNV | Missense_Mutation | novel | c.1814N>A | p.Thr605Lys | p.T605K | Q9UIG0 | protein_coding | deleterious(0.05) | possibly_damaging(0.829) | TCGA-A2-A25A-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unspecific | Cytoxan | SD |
BAZ1B | SNV | Missense_Mutation | c.2584N>A | p.Glu862Lys | p.E862K | Q9UIG0 | protein_coding | tolerated(0.39) | benign(0.015) | TCGA-A8-A06Q-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
BAZ1B | SNV | Missense_Mutation | c.1556G>A | p.Arg519Gln | p.R519Q | Q9UIG0 | protein_coding | tolerated(0.57) | benign(0.009) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
BAZ1B | SNV | Missense_Mutation | c.1476N>T | p.Arg492Ser | p.R492S | Q9UIG0 | protein_coding | deleterious(0.02) | benign(0.01) | TCGA-AN-A0AS-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
BAZ1B | SNV | Missense_Mutation | c.146N>A | p.Ile49Asn | p.I49N | Q9UIG0 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-BH-A0AY-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | SD | ||
BAZ1B | SNV | Missense_Mutation | novel | c.2438A>G | p.Asn813Ser | p.N813S | Q9UIG0 | protein_coding | tolerated(0.71) | benign(0.018) | TCGA-D8-A1XK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicine+cyclophosphamide | SD |
BAZ1B | SNV | Missense_Mutation | c.784T>G | p.Leu262Val | p.L262V | Q9UIG0 | protein_coding | tolerated(0.16) | probably_damaging(0.991) | TCGA-D8-A1XK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicine+cyclophosphamide | SD |
Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 |
Top |
Related drugs of malignant transformation related genes |
![]() |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
Page: 1 |