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Gene: DAXX |
Gene summary for DAXX |
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Gene information | Species | Human | Gene symbol | DAXX | Gene ID | 1616 |
Gene name | death domain associated protein | |
Gene Alias | BING2 | |
Cytomap | 6p21.32 | |
Gene Type | protein-coding | GO ID | GO:0001932 | UniProtAcc | A0A024RCS3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
1616 | DAXX | P48T-E | Human | Esophagus | ESCC | 3.24e-20 | 3.36e-01 | 0.0959 |
1616 | DAXX | P49T-E | Human | Esophagus | ESCC | 4.48e-15 | 1.33e+00 | 0.1768 |
1616 | DAXX | P52T-E | Human | Esophagus | ESCC | 1.29e-36 | 8.43e-01 | 0.1555 |
1616 | DAXX | P54T-E | Human | Esophagus | ESCC | 1.42e-33 | 7.56e-01 | 0.0975 |
1616 | DAXX | P56T-E | Human | Esophagus | ESCC | 6.04e-04 | 7.55e-01 | 0.1613 |
1616 | DAXX | P57T-E | Human | Esophagus | ESCC | 1.66e-19 | 3.12e-01 | 0.0926 |
1616 | DAXX | P61T-E | Human | Esophagus | ESCC | 1.03e-19 | 3.53e-01 | 0.099 |
1616 | DAXX | P62T-E | Human | Esophagus | ESCC | 9.28e-62 | 9.88e-01 | 0.1302 |
1616 | DAXX | P65T-E | Human | Esophagus | ESCC | 6.00e-34 | 5.24e-01 | 0.0978 |
1616 | DAXX | P74T-E | Human | Esophagus | ESCC | 8.20e-31 | 9.66e-01 | 0.1479 |
1616 | DAXX | P75T-E | Human | Esophagus | ESCC | 1.54e-40 | 9.83e-01 | 0.1125 |
1616 | DAXX | P76T-E | Human | Esophagus | ESCC | 1.85e-31 | 5.82e-01 | 0.1207 |
1616 | DAXX | P79T-E | Human | Esophagus | ESCC | 4.70e-27 | 5.76e-01 | 0.1154 |
1616 | DAXX | P80T-E | Human | Esophagus | ESCC | 3.36e-57 | 1.56e+00 | 0.155 |
1616 | DAXX | P82T-E | Human | Esophagus | ESCC | 3.80e-17 | 9.02e-01 | 0.1072 |
1616 | DAXX | P83T-E | Human | Esophagus | ESCC | 1.77e-33 | 8.70e-01 | 0.1738 |
1616 | DAXX | P84T-E | Human | Esophagus | ESCC | 9.79e-08 | 4.57e-01 | 0.0933 |
1616 | DAXX | P89T-E | Human | Esophagus | ESCC | 3.09e-22 | 1.43e+00 | 0.1752 |
1616 | DAXX | P91T-E | Human | Esophagus | ESCC | 3.54e-17 | 1.47e+00 | 0.1828 |
1616 | DAXX | P107T-E | Human | Esophagus | ESCC | 2.58e-47 | 1.02e+00 | 0.171 |
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∗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. |
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Malignant transformation related pathway analysis |
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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 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:1903320 | Colorectum | AD | regulation of protein modification by small protein conjugation or removal | 86/3918 | 242/18723 | 9.43e-08 | 4.65e-06 | 86 |
GO:0071383 | Colorectum | AD | cellular response to steroid hormone stimulus | 73/3918 | 204/18723 | 6.31e-07 | 2.24e-05 | 73 |
GO:0070997 | Colorectum | AD | neuron death | 114/3918 | 361/18723 | 1.13e-06 | 3.72e-05 | 114 |
GO:0030522 | Colorectum | AD | intracellular receptor signaling pathway | 87/3918 | 265/18723 | 3.69e-06 | 1.03e-04 | 87 |
GO:0031396 | Colorectum | AD | regulation of protein ubiquitination | 72/3918 | 210/18723 | 4.50e-06 | 1.21e-04 | 72 |
GO:0043401 | Colorectum | AD | steroid hormone mediated signaling pathway | 51/3918 | 136/18723 | 6.52e-06 | 1.63e-04 | 51 |
GO:1901214 | Colorectum | AD | regulation of neuron death | 99/3918 | 319/18723 | 1.26e-05 | 2.76e-04 | 99 |
GO:0048545 | Colorectum | AD | response to steroid hormone | 104/3918 | 339/18723 | 1.33e-05 | 2.90e-04 | 104 |
GO:0009755 | Colorectum | AD | hormone-mediated signaling pathway | 64/3918 | 190/18723 | 2.78e-05 | 5.24e-04 | 64 |
GO:0030518 | Colorectum | AD | intracellular steroid hormone receptor signaling pathway | 43/3918 | 116/18723 | 4.61e-05 | 7.97e-04 | 43 |
GO:0006325 | Colorectum | AD | chromatin organization | 119/3918 | 409/18723 | 4.85e-05 | 8.33e-04 | 119 |
GO:0035966 | Colorectum | AD | response to topologically incorrect protein | 54/3918 | 159/18723 | 8.85e-05 | 1.36e-03 | 54 |
GO:0035967 | Colorectum | AD | cellular response to topologically incorrect protein | 42/3918 | 116/18723 | 1.04e-04 | 1.56e-03 | 42 |
GO:0033674 | Colorectum | AD | positive regulation of kinase activity | 131/3918 | 467/18723 | 1.28e-04 | 1.85e-03 | 131 |
GO:0030521 | Colorectum | AD | androgen receptor signaling pathway | 20/3918 | 44/18723 | 2.26e-04 | 2.94e-03 | 20 |
GO:0097191 | Colorectum | AD | extrinsic apoptotic signaling pathway | 68/3918 | 219/18723 | 2.64e-04 | 3.27e-03 | 68 |
GO:0046686 | Colorectum | AD | response to cadmium ion | 27/3918 | 68/18723 | 3.19e-04 | 3.80e-03 | 27 |
GO:0010038 | Colorectum | AD | response to metal ion | 106/3918 | 373/18723 | 3.22e-04 | 3.83e-03 | 106 |
GO:0071276 | Colorectum | AD | cellular response to cadmium ion | 18/3918 | 40/18723 | 5.36e-04 | 5.74e-03 | 18 |
GO:0071248 | Colorectum | AD | cellular response to metal ion | 61/3918 | 197/18723 | 5.74e-04 | 6.09e-03 | 61 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa05012 | Colorectum | AD | Parkinson disease | 147/2092 | 266/8465 | 2.53e-27 | 8.48e-25 | 5.41e-25 | 147 |
hsa05014 | Colorectum | AD | Amyotrophic lateral sclerosis | 164/2092 | 364/8465 | 4.28e-18 | 1.27e-16 | 8.09e-17 | 164 |
hsa05022 | Colorectum | AD | Pathways of neurodegeneration - multiple diseases | 201/2092 | 476/8465 | 4.54e-18 | 1.27e-16 | 8.09e-17 | 201 |
hsa050121 | Colorectum | AD | Parkinson disease | 147/2092 | 266/8465 | 2.53e-27 | 8.48e-25 | 5.41e-25 | 147 |
hsa050141 | Colorectum | AD | Amyotrophic lateral sclerosis | 164/2092 | 364/8465 | 4.28e-18 | 1.27e-16 | 8.09e-17 | 164 |
hsa050221 | Colorectum | AD | Pathways of neurodegeneration - multiple diseases | 201/2092 | 476/8465 | 4.54e-18 | 1.27e-16 | 8.09e-17 | 201 |
hsa050122 | Colorectum | SER | Parkinson disease | 132/1580 | 266/8465 | 2.72e-31 | 9.03e-29 | 6.55e-29 | 132 |
hsa050222 | Colorectum | SER | Pathways of neurodegeneration - multiple diseases | 168/1580 | 476/8465 | 6.23e-19 | 2.07e-17 | 1.50e-17 | 168 |
hsa050142 | Colorectum | SER | Amyotrophic lateral sclerosis | 138/1580 | 364/8465 | 9.89e-19 | 2.99e-17 | 2.17e-17 | 138 |
hsa050123 | Colorectum | SER | Parkinson disease | 132/1580 | 266/8465 | 2.72e-31 | 9.03e-29 | 6.55e-29 | 132 |
hsa050223 | Colorectum | SER | Pathways of neurodegeneration - multiple diseases | 168/1580 | 476/8465 | 6.23e-19 | 2.07e-17 | 1.50e-17 | 168 |
hsa050143 | Colorectum | SER | Amyotrophic lateral sclerosis | 138/1580 | 364/8465 | 9.89e-19 | 2.99e-17 | 2.17e-17 | 138 |
hsa050124 | Colorectum | MSS | Parkinson disease | 140/1875 | 266/8465 | 2.32e-28 | 7.79e-26 | 4.77e-26 | 140 |
hsa050224 | Colorectum | MSS | Pathways of neurodegeneration - multiple diseases | 192/1875 | 476/8465 | 2.79e-20 | 1.04e-18 | 6.36e-19 | 192 |
hsa050144 | Colorectum | MSS | Amyotrophic lateral sclerosis | 156/1875 | 364/8465 | 1.43e-19 | 4.62e-18 | 2.83e-18 | 156 |
hsa04210 | Colorectum | MSS | Apoptosis | 44/1875 | 136/8465 | 3.66e-03 | 1.66e-02 | 1.01e-02 | 44 |
hsa050125 | Colorectum | MSS | Parkinson disease | 140/1875 | 266/8465 | 2.32e-28 | 7.79e-26 | 4.77e-26 | 140 |
hsa050225 | Colorectum | MSS | Pathways of neurodegeneration - multiple diseases | 192/1875 | 476/8465 | 2.79e-20 | 1.04e-18 | 6.36e-19 | 192 |
hsa050145 | Colorectum | MSS | Amyotrophic lateral sclerosis | 156/1875 | 364/8465 | 1.43e-19 | 4.62e-18 | 2.83e-18 | 156 |
hsa042101 | Colorectum | MSS | Apoptosis | 44/1875 | 136/8465 | 3.66e-03 | 1.66e-02 | 1.01e-02 | 44 |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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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. |
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Somatic mutation of malignant transformation related genes |
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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 |
DAXX | SNV | Missense_Mutation | novel | c.2185G>A | p.Asp729Asn | p.D729N | Q9UER7 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
DAXX | SNV | Missense_Mutation | c.1142T>G | p.Met381Arg | p.M381R | Q9UER7 | protein_coding | tolerated(0.42) | benign(0.359) | TCGA-AR-A24U-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD | |
DAXX | SNV | Missense_Mutation | rs758422357 | c.1042N>A | p.Val348Ile | p.V348I | Q9UER7 | protein_coding | tolerated(1) | benign(0.003) | TCGA-LD-A74U-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | taxotere | SD |
DAXX | SNV | Missense_Mutation | novel | c.427C>A | p.Leu143Met | p.L143M | Q9UER7 | protein_coding | tolerated(0.12) | benign(0.312) | TCGA-OL-A6VQ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
DAXX | SNV | Missense_Mutation | rs763046918 | c.2105N>T | p.Ser702Phe | p.S702F | Q9UER7 | protein_coding | tolerated(0.26) | benign(0.003) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
DAXX | SNV | Missense_Mutation | novel | c.514N>A | p.Glu172Lys | p.E172K | Q9UER7 | protein_coding | tolerated(0.16) | benign(0.111) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
DAXX | SNV | Missense_Mutation | rs375012684 | c.1318N>A | p.Asp440Asn | p.D440N | Q9UER7 | protein_coding | tolerated(0.17) | benign(0.085) | TCGA-AA-3811-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD |
DAXX | SNV | Missense_Mutation | c.8N>T | p.Thr3Ile | p.T3I | Q9UER7 | protein_coding | deleterious(0.02) | possibly_damaging(0.452) | TCGA-AU-6004-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
DAXX | SNV | Missense_Mutation | c.202N>A | p.Glu68Lys | p.E68K | Q9UER7 | protein_coding | tolerated(0.22) | benign(0.003) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
DAXX | SNV | Missense_Mutation | c.1210N>T | p.His404Tyr | p.H404Y | Q9UER7 | protein_coding | tolerated(0.46) | benign(0.158) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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