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Gene: CA1 |
Gene summary for CA1 |
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Gene information | Species | Human | Gene symbol | CA1 | Gene ID | 759 |
Gene name | carbonic anhydrase 1 | |
Gene Alias | CA-I | |
Cytomap | 8q21.2 | |
Gene Type | protein-coding | GO ID | GO:0006730 | UniProtAcc | P00915 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
759 | CA1 | HTA11_3410_2000001011 | Human | Colorectum | AD | 4.47e-04 | -2.33e-01 | 0.0155 |
759 | CA1 | HTA11_347_2000001011 | Human | Colorectum | AD | 5.04e-27 | 2.26e+00 | -0.1954 |
759 | CA1 | HTA11_411_2000001011 | Human | Colorectum | SER | 1.31e-02 | 2.07e+00 | -0.2602 |
759 | CA1 | HTA11_696_2000001011 | Human | Colorectum | AD | 8.28e-14 | 1.10e+00 | -0.1464 |
759 | CA1 | HTA11_866_2000001011 | Human | Colorectum | AD | 3.61e-02 | 6.63e-01 | -0.1001 |
759 | CA1 | HTA11_2992_2000001011 | Human | Colorectum | SER | 1.28e-09 | 3.25e+00 | -0.1706 |
759 | CA1 | HTA11_5212_2000001011 | Human | Colorectum | AD | 2.56e-25 | 3.91e+00 | -0.2061 |
759 | CA1 | HTA11_5216_2000001011 | Human | Colorectum | SER | 1.01e-06 | 2.38e+00 | -0.1462 |
759 | CA1 | HTA11_866_3004761011 | Human | Colorectum | AD | 1.76e-04 | -2.43e-01 | 0.096 |
759 | CA1 | HTA11_7696_3000711011 | Human | Colorectum | AD | 9.06e-05 | -2.30e-01 | 0.0674 |
759 | CA1 | HTA11_99999970781_79442 | Human | Colorectum | MSS | 6.27e-03 | -2.40e-01 | 0.294 |
759 | CA1 | HTA11_99999971662_82457 | Human | Colorectum | MSS | 1.49e-05 | -2.46e-01 | 0.3859 |
759 | CA1 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 5.76e-05 | -2.45e-01 | 0.3005 |
759 | CA1 | A001-C-207 | Human | Colorectum | FAP | 6.53e-06 | -2.50e-01 | 0.1278 |
759 | CA1 | A002-C-201 | Human | Colorectum | FAP | 4.40e-09 | -2.50e-01 | 0.0324 |
759 | CA1 | A002-C-203 | Human | Colorectum | FAP | 9.63e-08 | -2.47e-01 | 0.2786 |
759 | CA1 | A001-C-119 | Human | Colorectum | FAP | 1.41e-04 | -2.50e-01 | -0.1557 |
759 | CA1 | A001-C-108 | Human | Colorectum | FAP | 2.16e-03 | -2.07e-01 | -0.0272 |
759 | CA1 | A002-C-205 | Human | Colorectum | FAP | 1.28e-05 | -2.21e-01 | -0.1236 |
759 | CA1 | A014-C-108 | Human | Colorectum | FAP | 2.37e-02 | -2.31e-01 | -0.124 |
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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:000647916 | Thyroid | ATC | protein methylation | 85/6293 | 181/18723 | 1.27e-04 | 9.00e-04 | 85 |
GO:000821316 | Thyroid | ATC | protein alkylation | 85/6293 | 181/18723 | 1.27e-04 | 9.00e-04 | 85 |
GO:009730528 | Thyroid | ATC | response to alcohol | 113/6293 | 253/18723 | 1.53e-04 | 1.06e-03 | 113 |
GO:001038911 | Thyroid | ATC | regulation of G2/M transition of mitotic cell cycle | 49/6293 | 94/18723 | 1.60e-04 | 1.10e-03 | 49 |
GO:003106015 | Thyroid | ATC | regulation of histone methylation | 38/6293 | 69/18723 | 1.97e-04 | 1.31e-03 | 38 |
GO:004396611 | Thyroid | ATC | histone H3 acetylation | 34/6293 | 61/18723 | 3.10e-04 | 1.94e-03 | 34 |
GO:007135627 | Thyroid | ATC | cellular response to tumor necrosis factor | 102/6293 | 229/18723 | 3.52e-04 | 2.18e-03 | 102 |
GO:0051494110 | Thyroid | ATC | negative regulation of cytoskeleton organization | 76/6293 | 163/18723 | 3.68e-04 | 2.27e-03 | 76 |
GO:190274911 | Thyroid | ATC | regulation of cell cycle G2/M phase transition | 51/6293 | 102/18723 | 4.45e-04 | 2.64e-03 | 51 |
GO:000630212 | Thyroid | ATC | double-strand break repair | 110/6293 | 251/18723 | 4.48e-04 | 2.65e-03 | 110 |
GO:000704012 | Thyroid | ATC | lysosome organization | 39/6293 | 74/18723 | 5.41e-04 | 3.13e-03 | 39 |
GO:008017112 | Thyroid | ATC | lytic vacuole organization | 39/6293 | 74/18723 | 5.41e-04 | 3.13e-03 | 39 |
GO:003314414 | Thyroid | ATC | negative regulation of intracellular steroid hormone receptor signaling pathway | 23/6293 | 38/18723 | 6.05e-04 | 3.44e-03 | 23 |
GO:004576621 | Thyroid | ATC | positive regulation of angiogenesis | 82/6293 | 181/18723 | 6.79e-04 | 3.83e-03 | 82 |
GO:190401821 | Thyroid | ATC | positive regulation of vasculature development | 82/6293 | 181/18723 | 6.79e-04 | 3.83e-03 | 82 |
GO:000709511 | Thyroid | ATC | mitotic G2 DNA damage checkpoint | 21/6293 | 34/18723 | 7.12e-04 | 4.00e-03 | 21 |
GO:003506512 | Thyroid | ATC | regulation of histone acetylation | 30/6293 | 54/18723 | 7.41e-04 | 4.14e-03 | 30 |
GO:009023911 | Thyroid | ATC | regulation of histone H4 acetylation | 11/6293 | 14/18723 | 7.46e-04 | 4.14e-03 | 11 |
GO:007180631 | Thyroid | ATC | protein transmembrane transport | 32/6293 | 59/18723 | 8.74e-04 | 4.72e-03 | 32 |
GO:004398412 | Thyroid | ATC | histone H4-K16 acetylation | 14/6293 | 20/18723 | 9.60e-04 | 5.13e-03 | 14 |
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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 |
CA1 | SNV | Missense_Mutation | c.539T>G | p.Phe180Cys | p.F180C | P00915 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-BH-A1FJ-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
CA1 | SNV | Missense_Mutation | novel | c.83N>G | p.Asn28Ser | p.N28S | P00915 | protein_coding | deleterious(0.02) | benign(0.007) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
CA1 | SNV | Missense_Mutation | novel | c.13G>A | p.Asp5Asn | p.D5N | P00915 | protein_coding | tolerated(0.97) | benign(0) | TCGA-EA-A97N-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
CA1 | SNV | Missense_Mutation | rs141945543 | c.715G>A | p.Ala239Thr | p.A239T | P00915 | protein_coding | tolerated(0.3) | benign(0.333) | TCGA-AZ-4615-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | xeloda | PD |
CA1 | SNV | Missense_Mutation | c.208N>C | p.Asn70His | p.N70H | P00915 | protein_coding | deleterious(0.02) | possibly_damaging(0.733) | TCGA-CA-6718-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | PD | |
CA1 | insertion | Frame_Shift_Ins | novel | c.192_193insG | p.His65AlafsTer8 | p.H65Afs*8 | P00915 | protein_coding | TCGA-A6-5665-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | ||
CA1 | SNV | Missense_Mutation | c.40C>A | p.Pro14Thr | p.P14T | P00915 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
CA1 | SNV | Missense_Mutation | c.358N>A | p.His120Asn | p.H120N | P00915 | protein_coding | deleterious(0.01) | probably_damaging(1) | TCGA-AX-A05Z-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | SD | |
CA1 | SNV | Missense_Mutation | rs121909578 | c.740N>A | p.Arg247His | p.R247H | P00915 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD |
CA1 | SNV | Missense_Mutation | novel | c.344N>G | p.Tyr115Cys | p.Y115C | P00915 | protein_coding | deleterious(0) | probably_damaging(0.972) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | 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 |
759 | CA1 | DRUGGABLE GENOME, ENZYME | DICHLORPHENAMIDE | DICHLORPHENAMIDE | ||
759 | CA1 | DRUGGABLE GENOME, ENZYME | inhibitor | CHEMBL1200814 | ACETAZOLAMIDE SODIUM | |
759 | CA1 | DRUGGABLE GENOME, ENZYME | ZONISAMIDE | ZONISAMIDE | ||
759 | CA1 | DRUGGABLE GENOME, ENZYME | inhibitor | CHEMBL166863 | POLMACOXIB | |
759 | CA1 | DRUGGABLE GENOME, ENZYME | inhibitor | 178103435 | METHOCARBAMOL | |
759 | CA1 | DRUGGABLE GENOME, ENZYME | inhibitor | 178102191 | ||
759 | CA1 | DRUGGABLE GENOME, ENZYME | inhibitor | 381118859 | ||
759 | CA1 | DRUGGABLE GENOME, ENZYME | Ethoxzolamide | ETHOXZOLAMIDE | ||
759 | CA1 | DRUGGABLE GENOME, ENZYME | inhibitor | 178103398 | ACETAZOLAMIDE | |
759 | CA1 | DRUGGABLE GENOME, ENZYME | activator | 178100344 | HISTIDINE |
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