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Gene: GK |
Gene summary for GK |
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Gene information | Species | Human | Gene symbol | GK | Gene ID | 2710 |
Gene name | glycerol kinase | |
Gene Alias | GK1 | |
Cytomap | Xp21.2 | |
Gene Type | protein-coding | GO ID | GO:0005975 | UniProtAcc | B4DH54 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
2710 | GK | LZE20T | Human | Esophagus | ESCC | 2.64e-04 | 3.81e-01 | 0.0662 |
2710 | GK | LZE24T | Human | Esophagus | ESCC | 5.03e-06 | 1.70e-01 | 0.0596 |
2710 | GK | LZE21T | Human | Esophagus | ESCC | 1.01e-07 | 6.53e-01 | 0.0655 |
2710 | GK | LZE6T | Human | Esophagus | ESCC | 4.44e-08 | 5.59e-01 | 0.0845 |
2710 | GK | P1T-E | Human | Esophagus | ESCC | 2.39e-12 | 1.35e+00 | 0.0875 |
2710 | GK | P2T-E | Human | Esophagus | ESCC | 1.19e-09 | 2.12e-01 | 0.1177 |
2710 | GK | P8T-E | Human | Esophagus | ESCC | 6.50e-05 | 1.89e-01 | 0.0889 |
2710 | GK | P11T-E | Human | Esophagus | ESCC | 5.83e-07 | 2.10e-01 | 0.1426 |
2710 | GK | P12T-E | Human | Esophagus | ESCC | 4.51e-04 | 1.21e-01 | 0.1122 |
2710 | GK | P16T-E | Human | Esophagus | ESCC | 4.44e-10 | 2.05e-01 | 0.1153 |
2710 | GK | P21T-E | Human | Esophagus | ESCC | 1.34e-06 | 2.57e-01 | 0.1617 |
2710 | GK | P23T-E | Human | Esophagus | ESCC | 3.73e-22 | 1.20e+00 | 0.108 |
2710 | GK | P26T-E | Human | Esophagus | ESCC | 2.11e-09 | 2.23e-01 | 0.1276 |
2710 | GK | P27T-E | Human | Esophagus | ESCC | 3.44e-07 | 1.65e-01 | 0.1055 |
2710 | GK | P28T-E | Human | Esophagus | ESCC | 2.08e-03 | 2.04e-01 | 0.1149 |
2710 | GK | P37T-E | Human | Esophagus | ESCC | 1.09e-08 | 2.47e-01 | 0.1371 |
2710 | GK | P39T-E | Human | Esophagus | ESCC | 5.31e-08 | 2.55e-01 | 0.0894 |
2710 | GK | P47T-E | Human | Esophagus | ESCC | 2.16e-06 | 1.26e-01 | 0.1067 |
2710 | GK | P48T-E | Human | Esophagus | ESCC | 5.79e-06 | 1.28e-01 | 0.0959 |
2710 | GK | P52T-E | Human | Esophagus | ESCC | 4.03e-19 | 5.76e-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 |
GO:190118413 | Esophagus | ESCC | regulation of ERBB signaling pathway | 54/8552 | 79/18723 | 3.81e-05 | 3.08e-04 | 54 |
GO:00065063 | Esophagus | ESCC | GPI anchor biosynthetic process | 26/8552 | 32/18723 | 3.97e-05 | 3.21e-04 | 26 |
GO:00066505 | Esophagus | ESCC | glycerophospholipid metabolic process | 174/8552 | 306/18723 | 4.92e-05 | 3.85e-04 | 174 |
GO:000689818 | Esophagus | ESCC | receptor-mediated endocytosis | 142/8552 | 244/18723 | 5.22e-05 | 4.05e-04 | 142 |
GO:00420588 | Esophagus | ESCC | regulation of epidermal growth factor receptor signaling pathway | 50/8552 | 73/18723 | 6.75e-05 | 5.12e-04 | 50 |
GO:1903363110 | Esophagus | ESCC | negative regulation of cellular protein catabolic process | 51/8552 | 75/18723 | 7.70e-05 | 5.74e-04 | 51 |
GO:006191215 | Esophagus | ESCC | selective autophagy | 47/8552 | 68/18723 | 7.81e-05 | 5.80e-04 | 47 |
GO:005120416 | Esophagus | ESCC | protein insertion into mitochondrial membrane | 21/8552 | 25/18723 | 9.12e-05 | 6.54e-04 | 21 |
GO:00065053 | Esophagus | ESCC | GPI anchor metabolic process | 26/8552 | 33/18723 | 1.06e-04 | 7.43e-04 | 26 |
GO:00066541 | Esophagus | ESCC | phosphatidic acid biosynthetic process | 26/8552 | 33/18723 | 1.06e-04 | 7.43e-04 | 26 |
GO:0045861111 | Esophagus | ESCC | negative regulation of proteolysis | 195/8552 | 351/18723 | 1.13e-04 | 7.85e-04 | 195 |
GO:00331438 | Esophagus | ESCC | regulation of intracellular steroid hormone receptor signaling pathway | 50/8552 | 74/18723 | 1.16e-04 | 8.04e-04 | 50 |
GO:190010110 | Esophagus | ESCC | regulation of endoplasmic reticulum unfolded protein response | 24/8552 | 30/18723 | 1.27e-04 | 8.67e-04 | 24 |
GO:00442626 | Esophagus | ESCC | cellular carbohydrate metabolic process | 160/8552 | 283/18723 | 1.43e-04 | 9.66e-04 | 160 |
GO:1903051110 | Esophagus | ESCC | negative regulation of proteolysis involved in cellular protein catabolic process | 44/8552 | 64/18723 | 1.59e-04 | 1.05e-03 | 44 |
GO:000913219 | Esophagus | ESCC | nucleoside diphosphate metabolic process | 77/8552 | 124/18723 | 1.65e-04 | 1.09e-03 | 77 |
GO:007258314 | Esophagus | ESCC | clathrin-dependent endocytosis | 34/8552 | 47/18723 | 1.91e-04 | 1.21e-03 | 34 |
GO:00464733 | Esophagus | ESCC | phosphatidic acid metabolic process | 28/8552 | 37/18723 | 2.00e-04 | 1.26e-03 | 28 |
GO:001097516 | Esophagus | ESCC | regulation of neuron projection development | 240/8552 | 445/18723 | 2.48e-04 | 1.53e-03 | 240 |
GO:00510926 | Esophagus | ESCC | positive regulation of NF-kappaB transcription factor activity | 91/8552 | 152/18723 | 2.91e-04 | 1.75e-03 | 91 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa033206 | Liver | NAFLD | PPAR signaling pathway | 25/1043 | 75/8465 | 1.61e-06 | 6.62e-05 | 5.33e-05 | 25 |
hsa0332011 | Liver | NAFLD | PPAR signaling pathway | 25/1043 | 75/8465 | 1.61e-06 | 6.62e-05 | 5.33e-05 | 25 |
hsa0332021 | Liver | Cirrhotic | PPAR signaling pathway | 32/2530 | 75/8465 | 1.24e-02 | 3.92e-02 | 2.42e-02 | 32 |
hsa0332031 | Liver | Cirrhotic | PPAR signaling pathway | 32/2530 | 75/8465 | 1.24e-02 | 3.92e-02 | 2.42e-02 | 32 |
hsa033204 | Liver | HCC | PPAR signaling pathway | 48/4020 | 75/8465 | 2.83e-03 | 9.37e-03 | 5.21e-03 | 48 |
hsa005615 | Liver | HCC | Glycerolipid metabolism | 41/4020 | 63/8465 | 3.59e-03 | 1.12e-02 | 6.22e-03 | 41 |
hsa033205 | Liver | HCC | PPAR signaling pathway | 48/4020 | 75/8465 | 2.83e-03 | 9.37e-03 | 5.21e-03 | 48 |
hsa0056112 | Liver | HCC | Glycerolipid metabolism | 41/4020 | 63/8465 | 3.59e-03 | 1.12e-02 | 6.22e-03 | 41 |
hsa03320 | Stomach | GC | PPAR signaling pathway | 18/708 | 75/8465 | 3.26e-05 | 4.01e-04 | 2.82e-04 | 18 |
hsa005614 | Stomach | GC | Glycerolipid metabolism | 12/708 | 63/8465 | 5.36e-03 | 3.01e-02 | 2.12e-02 | 12 |
hsa033201 | Stomach | GC | PPAR signaling pathway | 18/708 | 75/8465 | 3.26e-05 | 4.01e-04 | 2.82e-04 | 18 |
hsa0056111 | Stomach | GC | Glycerolipid metabolism | 12/708 | 63/8465 | 5.36e-03 | 3.01e-02 | 2.12e-02 | 12 |
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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 |
GK | SNV | Missense_Mutation | c.65C>T | p.Ser22Leu | p.S22L | P32189 | protein_coding | deleterious(0) | possibly_damaging(0.874) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
GK | SNV | Missense_Mutation | rs772353152 | c.1256G>A | p.Arg419Gln | p.R419Q | P32189 | protein_coding | tolerated(0.32) | benign(0.003) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
GK | SNV | Missense_Mutation | c.11C>T | p.Ser4Leu | p.S4L | P32189 | protein_coding | tolerated(0.14) | benign(0.012) | TCGA-BH-A209-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
GK | SNV | Missense_Mutation | novel | c.1423G>C | p.Val475Leu | p.V475L | P32189 | protein_coding | tolerated(0.07) | benign(0.075) | TCGA-BH-A6R8-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
GK | SNV | Missense_Mutation | novel | c.772C>G | p.Pro258Ala | p.P258A | P32189 | protein_coding | deleterious(0.02) | probably_damaging(0.981) | TCGA-C5-A8XI-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | SD |
GK | SNV | Missense_Mutation | rs757334363 | c.1403N>T | p.Ala468Val | p.A468V | P32189 | protein_coding | tolerated(0.06) | benign(0.287) | TCGA-VS-A8QA-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
GK | SNV | Missense_Mutation | c.1654G>T | p.Ala552Ser | p.A552S | P32189 | protein_coding | tolerated(0.19) | probably_damaging(0.997) | TCGA-A6-5661-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
GK | SNV | Missense_Mutation | c.1258N>T | p.Asp420Tyr | p.D420Y | P32189 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
GK | SNV | Missense_Mutation | c.1527G>T | p.Trp509Cys | p.W509C | P32189 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-G4-6321-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Chemotherapy | fluorouracil | SD | |
GK | SNV | Missense_Mutation | c.1651G>A | p.Gly551Arg | p.G551R | P32189 | protein_coding | tolerated(0.35) | probably_damaging(0.99) | TCGA-NH-A5IV-01 | Colorectum | colon adenocarcinoma | Female | >=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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