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Gene: MED29 |
Gene summary for MED29 |
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Gene information | Species | Human | Gene symbol | MED29 | Gene ID | 55588 |
Gene name | mediator complex subunit 29 | |
Gene Alias | IXL | |
Cytomap | 19q13.2 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q9NX70 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
55588 | MED29 | LZE4T | Human | Esophagus | ESCC | 6.43e-11 | 4.22e-01 | 0.0811 |
55588 | MED29 | LZE5T | Human | Esophagus | ESCC | 1.56e-08 | 4.45e-01 | 0.0514 |
55588 | MED29 | LZE7T | Human | Esophagus | ESCC | 8.21e-13 | 4.33e-01 | 0.0667 |
55588 | MED29 | LZE8T | Human | Esophagus | ESCC | 6.31e-13 | 2.20e-01 | 0.067 |
55588 | MED29 | LZE20T | Human | Esophagus | ESCC | 6.53e-11 | 3.83e-01 | 0.0662 |
55588 | MED29 | LZE21D1 | Human | Esophagus | HGIN | 1.02e-04 | 6.12e-01 | 0.0632 |
55588 | MED29 | LZE24T | Human | Esophagus | ESCC | 3.38e-26 | 5.96e-01 | 0.0596 |
55588 | MED29 | LZE21T | Human | Esophagus | ESCC | 5.15e-06 | 2.91e-01 | 0.0655 |
55588 | MED29 | LZE6T | Human | Esophagus | ESCC | 3.57e-07 | 4.00e-01 | 0.0845 |
55588 | MED29 | P1T-E | Human | Esophagus | ESCC | 4.34e-38 | 1.95e+00 | 0.0875 |
55588 | MED29 | P2T-E | Human | Esophagus | ESCC | 1.37e-35 | 6.10e-01 | 0.1177 |
55588 | MED29 | P4T-E | Human | Esophagus | ESCC | 2.22e-27 | 5.17e-01 | 0.1323 |
55588 | MED29 | P5T-E | Human | Esophagus | ESCC | 9.76e-33 | 5.71e-01 | 0.1327 |
55588 | MED29 | P8T-E | Human | Esophagus | ESCC | 1.60e-47 | 8.40e-01 | 0.0889 |
55588 | MED29 | P9T-E | Human | Esophagus | ESCC | 2.82e-12 | 1.92e-01 | 0.1131 |
55588 | MED29 | P10T-E | Human | Esophagus | ESCC | 1.97e-37 | 6.05e-01 | 0.116 |
55588 | MED29 | P11T-E | Human | Esophagus | ESCC | 3.99e-23 | 9.34e-01 | 0.1426 |
55588 | MED29 | P12T-E | Human | Esophagus | ESCC | 9.62e-35 | 4.98e-01 | 0.1122 |
55588 | MED29 | P15T-E | Human | Esophagus | ESCC | 6.29e-32 | 5.25e-01 | 0.1149 |
55588 | MED29 | P16T-E | Human | Esophagus | ESCC | 2.96e-23 | 3.38e-01 | 0.1153 |
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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). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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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 |
MED29 | SNV | Missense_Mutation | rs765711223 | c.63N>C | p.Lys21Asn | p.K21N | protein_coding | deleterious_low_confidence(0.02) | benign(0) | TCGA-C5-A8XH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
MED29 | SNV | Missense_Mutation | c.225C>G | p.Phe75Leu | p.F75L | protein_coding | tolerated(0.5) | probably_damaging(0.992) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | ||
MED29 | SNV | Missense_Mutation | c.285G>C | p.Leu95Phe | p.L95F | protein_coding | deleterious(0.01) | probably_damaging(0.94) | TCGA-Q1-A73O-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | ||
MED29 | SNV | Missense_Mutation | c.116N>G | p.Ser39Trp | p.S39W | protein_coding | deleterious(0.03) | possibly_damaging(0.877) | TCGA-VS-A9UC-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | SD | ||
MED29 | SNV | Missense_Mutation | novel | c.290A>G | p.Lys97Arg | p.K97R | protein_coding | tolerated(0.21) | benign(0.027) | TCGA-AA-3972-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | capecitabine | PD | |
MED29 | SNV | Missense_Mutation | c.274C>A | p.Leu92Ile | p.L92I | protein_coding | deleterious(0.03) | probably_damaging(0.998) | TCGA-AA-A024-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | ||
MED29 | SNV | Missense_Mutation | novel | c.218N>G | p.Gln73Arg | p.Q73R | protein_coding | deleterious(0) | probably_damaging(0.992) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
MED29 | SNV | Missense_Mutation | novel | c.356C>T | p.Pro119Leu | p.P119L | protein_coding | tolerated(0.09) | benign(0.003) | TCGA-AX-A06F-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | SD | |
MED29 | SNV | Missense_Mutation | c.390C>A | p.Phe130Leu | p.F130L | protein_coding | deleterious(0.01) | possibly_damaging(0.514) | TCGA-BS-A0UV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | ||
MED29 | SNV | Missense_Mutation | novel | c.565N>G | p.Ile189Val | p.I189V | protein_coding | tolerated(0.47) | probably_damaging(0.981) | TCGA-FI-A2D5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatinum | 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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