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Gene: GNAQ |
Gene summary for GNAQ |
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Gene information | Species | Human | Gene symbol | GNAQ | Gene ID | 2776 |
Gene name | G protein subunit alpha q | |
Gene Alias | CMC1 | |
Cytomap | 9q21.2 | |
Gene Type | protein-coding | GO ID | GO:0001508 | UniProtAcc | A0A024R240 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
2776 | GNAQ | CCI_1 | Human | Cervix | CC | 2.09e-04 | 7.33e-01 | 0.528 |
2776 | GNAQ | CCI_2 | Human | Cervix | CC | 4.09e-09 | 1.21e+00 | 0.5249 |
2776 | GNAQ | CCI_3 | Human | Cervix | CC | 2.22e-14 | 1.21e+00 | 0.516 |
2776 | GNAQ | L1 | Human | Cervix | CC | 2.51e-02 | -2.87e-01 | 0.0802 |
2776 | GNAQ | HTA11_3410_2000001011 | Human | Colorectum | AD | 4.06e-31 | -7.37e-01 | 0.0155 |
2776 | GNAQ | HTA11_2951_2000001011 | Human | Colorectum | AD | 1.76e-03 | -5.83e-01 | 0.0216 |
2776 | GNAQ | HTA11_347_2000001011 | Human | Colorectum | AD | 1.08e-16 | 8.00e-01 | -0.1954 |
2776 | GNAQ | HTA11_411_2000001011 | Human | Colorectum | SER | 6.59e-18 | 8.84e-01 | -0.2602 |
2776 | GNAQ | HTA11_5216_2000001011 | Human | Colorectum | SER | 7.79e-05 | -4.20e-01 | -0.1462 |
2776 | GNAQ | HTA11_9341_2000001011 | Human | Colorectum | SER | 3.28e-03 | -4.91e-01 | -0.00410000000000005 |
2776 | GNAQ | HTA11_866_3004761011 | Human | Colorectum | AD | 4.47e-17 | -6.48e-01 | 0.096 |
2776 | GNAQ | HTA11_8622_2000001021 | Human | Colorectum | SER | 3.21e-08 | -5.34e-01 | 0.0528 |
2776 | GNAQ | HTA11_10711_2000001011 | Human | Colorectum | AD | 3.97e-03 | -4.47e-01 | 0.0338 |
2776 | GNAQ | HTA11_7696_3000711011 | Human | Colorectum | AD | 7.87e-24 | -5.96e-01 | 0.0674 |
2776 | GNAQ | HTA11_99999970781_79442 | Human | Colorectum | MSS | 5.94e-11 | -4.52e-01 | 0.294 |
2776 | GNAQ | HTA11_99999965062_69753 | Human | Colorectum | MSI-H | 2.38e-03 | 5.98e-01 | 0.3487 |
2776 | GNAQ | HTA11_99999971662_82457 | Human | Colorectum | MSS | 1.70e-28 | -7.57e-01 | 0.3859 |
2776 | GNAQ | HTA11_99999973899_84307 | Human | Colorectum | MSS | 4.66e-09 | -7.39e-01 | 0.2585 |
2776 | GNAQ | HTA11_99999974143_84620 | Human | Colorectum | MSS | 2.40e-64 | -1.03e+00 | 0.3005 |
2776 | GNAQ | F007 | Human | Colorectum | FAP | 1.19e-05 | -4.57e-01 | 0.1176 |
Page: 1 2 3 4 5 6 7 8 9 |
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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:004206010 | Cervix | CC | wound healing | 109/2311 | 422/18723 | 1.84e-14 | 1.57e-11 | 109 |
GO:00160557 | Cervix | CC | Wnt signaling pathway | 98/2311 | 444/18723 | 4.82e-09 | 4.65e-07 | 98 |
GO:01987387 | Cervix | CC | cell-cell signaling by wnt | 98/2311 | 446/18723 | 6.16e-09 | 5.58e-07 | 98 |
GO:00301117 | Cervix | CC | regulation of Wnt signaling pathway | 76/2311 | 328/18723 | 3.05e-08 | 2.08e-06 | 76 |
GO:00608287 | Cervix | CC | regulation of canonical Wnt signaling pathway | 58/2311 | 253/18723 | 1.83e-06 | 5.89e-05 | 58 |
GO:00600707 | Cervix | CC | canonical Wnt signaling pathway | 66/2311 | 303/18723 | 2.47e-06 | 7.35e-05 | 66 |
GO:005134810 | Cervix | CC | negative regulation of transferase activity | 60/2311 | 268/18723 | 2.77e-06 | 8.02e-05 | 60 |
GO:00485118 | Cervix | CC | rhythmic process | 65/2311 | 298/18723 | 2.79e-06 | 8.04e-05 | 65 |
GO:004593610 | Cervix | CC | negative regulation of phosphate metabolic process | 88/2311 | 441/18723 | 2.92e-06 | 8.27e-05 | 88 |
GO:005087810 | Cervix | CC | regulation of body fluid levels | 78/2311 | 379/18723 | 3.20e-06 | 8.77e-05 | 78 |
GO:001056310 | Cervix | CC | negative regulation of phosphorus metabolic process | 88/2311 | 442/18723 | 3.21e-06 | 8.77e-05 | 88 |
GO:004232610 | Cervix | CC | negative regulation of phosphorylation | 77/2311 | 385/18723 | 1.09e-05 | 2.38e-04 | 77 |
GO:003164710 | Cervix | CC | regulation of protein stability | 63/2311 | 298/18723 | 1.14e-05 | 2.45e-04 | 63 |
GO:000193310 | Cervix | CC | negative regulation of protein phosphorylation | 69/2311 | 342/18723 | 2.29e-05 | 4.01e-04 | 69 |
GO:00093149 | Cervix | CC | response to radiation | 86/2311 | 456/18723 | 3.50e-05 | 5.63e-04 | 86 |
GO:000646910 | Cervix | CC | negative regulation of protein kinase activity | 47/2311 | 212/18723 | 4.13e-05 | 6.36e-04 | 47 |
GO:005082110 | Cervix | CC | protein stabilization | 43/2311 | 191/18723 | 5.90e-05 | 8.54e-04 | 43 |
GO:00076238 | Cervix | CC | circadian rhythm | 46/2311 | 210/18723 | 6.76e-05 | 9.60e-04 | 46 |
GO:00336739 | Cervix | CC | negative regulation of kinase activity | 50/2311 | 237/18723 | 9.22e-05 | 1.21e-03 | 50 |
GO:00508176 | Cervix | CC | coagulation | 45/2311 | 222/18723 | 5.08e-04 | 4.94e-03 | 45 |
Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0501041 | Stomach | CSG | Alzheimer disease | 71/633 | 384/8465 | 3.27e-13 | 7.94e-12 | 5.71e-12 | 71 |
hsa0516341 | Stomach | CSG | Human cytomegalovirus infection | 31/633 | 225/8465 | 6.37e-04 | 4.80e-03 | 3.45e-03 | 31 |
hsa0517041 | Stomach | CSG | Human immunodeficiency virus 1 infection | 29/633 | 212/8465 | 1.06e-03 | 7.60e-03 | 5.47e-03 | 29 |
hsa0513541 | Stomach | CSG | Yersinia infection | 20/633 | 137/8465 | 2.84e-03 | 1.84e-02 | 1.32e-02 | 20 |
hsa0491541 | Stomach | CSG | Estrogen signaling pathway | 20/633 | 138/8465 | 3.10e-03 | 1.88e-02 | 1.35e-02 | 20 |
hsa051462 | Stomach | CSG | Amoebiasis | 15/633 | 102/8465 | 8.50e-03 | 4.56e-02 | 3.28e-02 | 15 |
hsa0501651 | Stomach | CSG | Huntington disease | 68/633 | 306/8465 | 7.35e-17 | 2.90e-15 | 2.09e-15 | 68 |
hsa0502251 | Stomach | CSG | Pathways of neurodegeneration - multiple diseases | 82/633 | 476/8465 | 2.32e-13 | 6.67e-12 | 4.80e-12 | 82 |
hsa0501051 | Stomach | CSG | Alzheimer disease | 71/633 | 384/8465 | 3.27e-13 | 7.94e-12 | 5.71e-12 | 71 |
hsa0516351 | Stomach | CSG | Human cytomegalovirus infection | 31/633 | 225/8465 | 6.37e-04 | 4.80e-03 | 3.45e-03 | 31 |
hsa0517051 | Stomach | CSG | Human immunodeficiency virus 1 infection | 29/633 | 212/8465 | 1.06e-03 | 7.60e-03 | 5.47e-03 | 29 |
hsa0513551 | Stomach | CSG | Yersinia infection | 20/633 | 137/8465 | 2.84e-03 | 1.84e-02 | 1.32e-02 | 20 |
hsa0491551 | Stomach | CSG | Estrogen signaling pathway | 20/633 | 138/8465 | 3.10e-03 | 1.88e-02 | 1.35e-02 | 20 |
hsa051463 | Stomach | CSG | Amoebiasis | 15/633 | 102/8465 | 8.50e-03 | 4.56e-02 | 3.28e-02 | 15 |
Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 |
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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 |
GNAQ | SNV | Missense_Mutation | novel | c.492N>T | p.Leu164Phe | p.L164F | P50148 | protein_coding | deleterious(0.02) | possibly_damaging(0.456) | TCGA-AN-A0AT-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
GNAQ | SNV | Missense_Mutation | novel | c.75C>G | p.Ile25Met | p.I25M | P50148 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-C8-A8HQ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
GNAQ | SNV | Missense_Mutation | rs769002669 | c.676N>G | p.Ile226Val | p.I226V | P50148 | protein_coding | tolerated(0.06) | benign(0.106) | TCGA-FU-A40J-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Chemotherapy | carboplatin | CR |
GNAQ | SNV | Missense_Mutation | c.955G>A | p.Asp319Asn | p.D319N | P50148 | protein_coding | tolerated(0.19) | benign(0.014) | TCGA-Q1-A73O-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
GNAQ | SNV | Missense_Mutation | rs397514698 | c.548N>A | p.Arg183Gln | p.R183Q | P50148 | protein_coding | deleterious(0.03) | probably_damaging(0.958) | TCGA-A6-5665-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
GNAQ | SNV | Missense_Mutation | c.542N>C | p.Arg181Thr | p.R181T | P50148 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-AA-3666-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | PD | |
GNAQ | SNV | Missense_Mutation | c.403T>G | p.Leu135Val | p.L135V | P50148 | protein_coding | tolerated(0.06) | benign(0.118) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
GNAQ | SNV | Missense_Mutation | c.524C>T | p.Thr175Met | p.T175M | P50148 | protein_coding | deleterious(0) | probably_damaging(0.987) | TCGA-AD-5900-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
GNAQ | SNV | Missense_Mutation | rs761634659 | c.254N>T | p.Thr85Met | p.T85M | P50148 | protein_coding | tolerated(0.42) | benign(0.015) | TCGA-AZ-6601-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
GNAQ | SNV | Missense_Mutation | c.152G>T | p.Gly51Val | p.G51V | P50148 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-CM-4743-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Chemotherapy | capecitabine | 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 |
2776 | GNAQ | CLINICALLY ACTIONABLE, DRUG RESISTANCE | Verteporfin | VERTEPORFIN | 27308390 | |
2776 | GNAQ | CLINICALLY ACTIONABLE, DRUG RESISTANCE | SOTRASTAURIN ACETATE | 24141786 | ||
2776 | GNAQ | CLINICALLY ACTIONABLE, DRUG RESISTANCE | Everolimus | EVEROLIMUS | 27507190 | |
2776 | GNAQ | CLINICALLY ACTIONABLE, DRUG RESISTANCE | MEK INHIBITOR PD0325901 | 24141786 | ||
2776 | GNAQ | CLINICALLY ACTIONABLE, DRUG RESISTANCE | PLX4720 | PLX-4720 | 24504448 | |
2776 | GNAQ | CLINICALLY ACTIONABLE, DRUG RESISTANCE | Selumetinib | SELUMETINIB | 22550165 | |
2776 | GNAQ | CLINICALLY ACTIONABLE, DRUG RESISTANCE | CGM097 | CGM-097 | 27507190 | |
2776 | GNAQ | CLINICALLY ACTIONABLE, DRUG RESISTANCE | U0126 | 19078957 | ||
2776 | GNAQ | CLINICALLY ACTIONABLE, DRUG RESISTANCE | MEK162 | BINIMETINIB | 27507190 | |
2776 | GNAQ | CLINICALLY ACTIONABLE, DRUG RESISTANCE | Refametinib | REFAMETINIB | 23434733 |
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