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Gene: KCNJ15 |
Gene summary for KCNJ15 |
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Gene information | Species | Human | Gene symbol | KCNJ15 | Gene ID | 3772 |
Gene name | potassium inwardly rectifying channel subfamily J member 15 | |
Gene Alias | IRKK | |
Cytomap | 21q22.13-q22.2 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | Q99712 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
3772 | KCNJ15 | LZE4T | Human | Esophagus | ESCC | 2.57e-05 | 2.08e-01 | 0.0811 |
3772 | KCNJ15 | LZE8T | Human | Esophagus | ESCC | 4.22e-05 | 2.10e-01 | 0.067 |
3772 | KCNJ15 | P2T-E | Human | Esophagus | ESCC | 2.91e-06 | -1.98e-02 | 0.1177 |
3772 | KCNJ15 | P4T-E | Human | Esophagus | ESCC | 6.11e-13 | 1.02e-01 | 0.1323 |
3772 | KCNJ15 | P5T-E | Human | Esophagus | ESCC | 8.35e-04 | -6.41e-02 | 0.1327 |
3772 | KCNJ15 | P9T-E | Human | Esophagus | ESCC | 1.44e-08 | 1.38e-01 | 0.1131 |
3772 | KCNJ15 | P10T-E | Human | Esophagus | ESCC | 9.11e-19 | 4.79e-01 | 0.116 |
3772 | KCNJ15 | P11T-E | Human | Esophagus | ESCC | 5.58e-05 | 4.58e-01 | 0.1426 |
3772 | KCNJ15 | P15T-E | Human | Esophagus | ESCC | 2.89e-12 | 2.73e-01 | 0.1149 |
3772 | KCNJ15 | P21T-E | Human | Esophagus | ESCC | 1.04e-21 | 5.09e-01 | 0.1617 |
3772 | KCNJ15 | P22T-E | Human | Esophagus | ESCC | 5.63e-29 | 6.49e-01 | 0.1236 |
3772 | KCNJ15 | P26T-E | Human | Esophagus | ESCC | 1.70e-17 | 4.24e-01 | 0.1276 |
3772 | KCNJ15 | P27T-E | Human | Esophagus | ESCC | 3.15e-07 | 1.30e-01 | 0.1055 |
3772 | KCNJ15 | P28T-E | Human | Esophagus | ESCC | 4.52e-07 | 1.72e-01 | 0.1149 |
3772 | KCNJ15 | P30T-E | Human | Esophagus | ESCC | 4.12e-12 | 2.99e-01 | 0.137 |
3772 | KCNJ15 | P31T-E | Human | Esophagus | ESCC | 6.16e-15 | 4.77e-01 | 0.1251 |
3772 | KCNJ15 | P37T-E | Human | Esophagus | ESCC | 2.34e-08 | 1.71e-01 | 0.1371 |
3772 | KCNJ15 | P42T-E | Human | Esophagus | ESCC | 1.45e-06 | 2.15e-01 | 0.1175 |
3772 | KCNJ15 | P48T-E | Human | Esophagus | ESCC | 2.54e-08 | 1.46e-01 | 0.0959 |
3772 | KCNJ15 | P52T-E | Human | Esophagus | ESCC | 8.44e-16 | 3.78e-01 | 0.1555 |
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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 |
hsa0497112 | Lung | IAC | Gastric acid secretion | 17/1053 | 76/8465 | 1.08e-02 | 3.93e-02 | 2.61e-02 | 17 |
hsa0497113 | Lung | IAC | Gastric acid secretion | 17/1053 | 76/8465 | 1.08e-02 | 3.93e-02 | 2.61e-02 | 17 |
hsa0497121 | Lung | AIS | Gastric acid secretion | 16/961 | 76/8465 | 1.02e-02 | 4.28e-02 | 2.74e-02 | 16 |
hsa0497131 | Lung | AIS | Gastric acid secretion | 16/961 | 76/8465 | 1.02e-02 | 4.28e-02 | 2.74e-02 | 16 |
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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 |
KCNJ15 | SNV | Missense_Mutation | c.59N>T | p.Ala20Val | p.A20V | Q99712 | protein_coding | tolerated(0.35) | benign(0) | TCGA-BR-6452-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
KCNJ15 | SNV | Missense_Mutation | c.559N>G | p.Thr187Ala | p.T187A | Q99712 | protein_coding | tolerated(0.79) | benign(0.007) | TCGA-BR-7851-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
KCNJ15 | SNV | Missense_Mutation | c.464N>C | p.Leu155Ser | p.L155S | Q99712 | protein_coding | deleterious(0) | possibly_damaging(0.904) | TCGA-BR-8363-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
KCNJ15 | SNV | Missense_Mutation | rs566041159 | c.521N>A | p.Arg174Gln | p.R174Q | Q99712 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-CG-5721-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | SD |
KCNJ15 | SNV | Missense_Mutation | c.131N>G | p.Asp44Gly | p.D44G | Q99712 | protein_coding | tolerated(0.15) | benign(0.253) | TCGA-CG-5723-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
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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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