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Gene: ANG |
Gene summary for ANG |
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Gene information | Species | Human | Gene symbol | ANG | Gene ID | 283 |
Gene name | angiogenin | |
Gene Alias | ALS9 | |
Cytomap | 14q11.2 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | P03950 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
283 | ANG | HTA11_3410_2000001011 | Human | Colorectum | AD | 1.41e-07 | 1.84e-01 | 0.0155 |
283 | ANG | HTA11_2487_2000001011 | Human | Colorectum | SER | 8.14e-15 | 4.33e-01 | -0.1808 |
283 | ANG | HTA11_1938_2000001011 | Human | Colorectum | AD | 3.84e-10 | 3.71e-01 | -0.0811 |
283 | ANG | HTA11_78_2000001011 | Human | Colorectum | AD | 2.54e-12 | 3.19e-01 | -0.1088 |
283 | ANG | HTA11_347_2000001011 | Human | Colorectum | AD | 1.18e-22 | 4.53e-01 | -0.1954 |
283 | ANG | HTA11_411_2000001011 | Human | Colorectum | SER | 3.33e-15 | 1.24e+00 | -0.2602 |
283 | ANG | HTA11_2112_2000001011 | Human | Colorectum | SER | 8.76e-08 | 6.35e-01 | -0.2196 |
283 | ANG | HTA11_3361_2000001011 | Human | Colorectum | AD | 7.49e-10 | 3.09e-01 | -0.1207 |
283 | ANG | HTA11_83_2000001011 | Human | Colorectum | SER | 1.12e-08 | 3.22e-01 | -0.1526 |
283 | ANG | HTA11_696_2000001011 | Human | Colorectum | AD | 5.54e-31 | 5.89e-01 | -0.1464 |
283 | ANG | HTA11_866_2000001011 | Human | Colorectum | AD | 1.42e-14 | 3.27e-01 | -0.1001 |
283 | ANG | HTA11_1391_2000001011 | Human | Colorectum | AD | 5.65e-19 | 4.31e-01 | -0.059 |
283 | ANG | HTA11_2992_2000001011 | Human | Colorectum | SER | 1.72e-05 | 3.79e-01 | -0.1706 |
283 | ANG | HTA11_5212_2000001011 | Human | Colorectum | AD | 2.47e-14 | 5.15e-01 | -0.2061 |
283 | ANG | HTA11_5216_2000001011 | Human | Colorectum | SER | 3.40e-02 | 2.52e-01 | -0.1462 |
283 | ANG | HTA11_546_2000001011 | Human | Colorectum | AD | 1.43e-09 | 3.74e-01 | -0.0842 |
283 | ANG | HTA11_7862_2000001011 | Human | Colorectum | AD | 3.08e-04 | 1.98e-01 | -0.0179 |
283 | ANG | HTA11_866_3004761011 | Human | Colorectum | AD | 3.29e-15 | 2.98e-01 | 0.096 |
283 | ANG | HTA11_4255_2000001011 | Human | Colorectum | SER | 2.49e-08 | 4.15e-01 | 0.0446 |
283 | ANG | HTA11_8622_2000001021 | Human | Colorectum | SER | 3.19e-02 | 2.05e-01 | 0.0528 |
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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:005123527 | Skin | cSCC | maintenance of location | 106/4864 | 327/18723 | 5.17e-03 | 2.61e-02 | 106 |
GO:005165128 | Skin | cSCC | maintenance of location in cell | 72/4864 | 214/18723 | 7.37e-03 | 3.47e-02 | 72 |
GO:003111315 | Skin | cSCC | regulation of microtubule polymerization | 23/4864 | 55/18723 | 7.54e-03 | 3.53e-02 | 23 |
GO:000173821 | Skin | cSCC | morphogenesis of a polarized epithelium | 35/4864 | 94/18723 | 1.05e-02 | 4.61e-02 | 35 |
GO:00513466 | Stomach | GC | negative regulation of hydrolase activity | 51/1159 | 379/18723 | 1.38e-07 | 8.14e-06 | 51 |
GO:0055088 | Stomach | GC | lipid homeostasis | 24/1159 | 167/18723 | 9.86e-05 | 2.00e-03 | 24 |
GO:00362936 | Stomach | GC | response to decreased oxygen levels | 36/1159 | 322/18723 | 4.36e-04 | 6.47e-03 | 36 |
GO:0060192 | Stomach | GC | negative regulation of lipase activity | 6/1159 | 18/18723 | 5.40e-04 | 7.55e-03 | 6 |
GO:00016666 | Stomach | GC | response to hypoxia | 34/1159 | 307/18723 | 7.34e-04 | 9.54e-03 | 34 |
GO:00704826 | Stomach | GC | response to oxygen levels | 37/1159 | 347/18723 | 8.94e-04 | 1.10e-02 | 37 |
GO:0051004 | Stomach | GC | regulation of lipoprotein lipase activity | 6/1159 | 20/18723 | 1.01e-03 | 1.20e-02 | 6 |
GO:0032386111 | Thyroid | PTC | regulation of intracellular transport | 202/5968 | 337/18723 | 1.12e-26 | 3.93e-24 | 202 |
GO:0033157112 | Thyroid | PTC | regulation of intracellular protein transport | 149/5968 | 229/18723 | 3.83e-25 | 1.15e-22 | 149 |
GO:0006913112 | Thyroid | PTC | nucleocytoplasmic transport | 181/5968 | 301/18723 | 2.93e-24 | 7.69e-22 | 181 |
GO:0051169112 | Thyroid | PTC | nuclear transport | 181/5968 | 301/18723 | 2.93e-24 | 7.69e-22 | 181 |
GO:0034504111 | Thyroid | PTC | protein localization to nucleus | 170/5968 | 290/18723 | 3.34e-21 | 6.38e-19 | 170 |
GO:0051168112 | Thyroid | PTC | nuclear export | 102/5968 | 154/18723 | 1.78e-18 | 2.01e-16 | 102 |
GO:004682223 | Thyroid | PTC | regulation of nucleocytoplasmic transport | 76/5968 | 106/18723 | 4.11e-17 | 3.70e-15 | 76 |
GO:0045185113 | Thyroid | PTC | maintenance of protein location | 64/5968 | 94/18723 | 5.92e-13 | 2.85e-11 | 64 |
GO:0006611110 | Thyroid | PTC | protein export from nucleus | 43/5968 | 57/18723 | 1.73e-11 | 6.81e-10 | 43 |
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 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa05014 | Colorectum | AD | Amyotrophic lateral sclerosis | 164/2092 | 364/8465 | 4.28e-18 | 1.27e-16 | 8.09e-17 | 164 |
hsa050141 | Colorectum | AD | Amyotrophic lateral sclerosis | 164/2092 | 364/8465 | 4.28e-18 | 1.27e-16 | 8.09e-17 | 164 |
hsa050142 | Colorectum | SER | Amyotrophic lateral sclerosis | 138/1580 | 364/8465 | 9.89e-19 | 2.99e-17 | 2.17e-17 | 138 |
hsa050143 | Colorectum | SER | Amyotrophic lateral sclerosis | 138/1580 | 364/8465 | 9.89e-19 | 2.99e-17 | 2.17e-17 | 138 |
hsa050144 | Colorectum | MSS | Amyotrophic lateral sclerosis | 156/1875 | 364/8465 | 1.43e-19 | 4.62e-18 | 2.83e-18 | 156 |
hsa050145 | Colorectum | MSS | Amyotrophic lateral sclerosis | 156/1875 | 364/8465 | 1.43e-19 | 4.62e-18 | 2.83e-18 | 156 |
hsa050146 | Colorectum | MSI-H | Amyotrophic lateral sclerosis | 95/797 | 364/8465 | 2.31e-21 | 1.50e-19 | 1.26e-19 | 95 |
hsa050147 | Colorectum | MSI-H | Amyotrophic lateral sclerosis | 95/797 | 364/8465 | 2.31e-21 | 1.50e-19 | 1.26e-19 | 95 |
hsa05014210 | Esophagus | ESCC | Amyotrophic lateral sclerosis | 266/4205 | 364/8465 | 1.31e-20 | 2.20e-18 | 1.13e-18 | 266 |
hsa0501438 | Esophagus | ESCC | Amyotrophic lateral sclerosis | 266/4205 | 364/8465 | 1.31e-20 | 2.20e-18 | 1.13e-18 | 266 |
hsa0501414 | Liver | Cirrhotic | Amyotrophic lateral sclerosis | 187/2530 | 364/8465 | 1.56e-18 | 6.50e-17 | 4.01e-17 | 187 |
hsa0501415 | Liver | Cirrhotic | Amyotrophic lateral sclerosis | 187/2530 | 364/8465 | 1.56e-18 | 6.50e-17 | 4.01e-17 | 187 |
hsa0501422 | Liver | HCC | Amyotrophic lateral sclerosis | 252/4020 | 364/8465 | 8.85e-18 | 7.41e-16 | 4.12e-16 | 252 |
hsa0501432 | Liver | HCC | Amyotrophic lateral sclerosis | 252/4020 | 364/8465 | 8.85e-18 | 7.41e-16 | 4.12e-16 | 252 |
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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 |
ANG | SNV | Missense_Mutation | c.265C>G | p.His89Asp | p.H89D | P03950 | protein_coding | deleterious(0) | benign(0.003) | TCGA-C5-A8XH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
ANG | SNV | Missense_Mutation | rs141398857 | c.356N>A | p.Arg119Gln | p.R119Q | P03950 | protein_coding | deleterious(0.01) | possibly_damaging(0.463) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ANG | SNV | Missense_Mutation | rs146485834 | c.224G>A | p.Arg75His | p.R75H | P03950 | protein_coding | tolerated(0.1) | benign(0.015) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ANG | SNV | Missense_Mutation | novel | c.269N>T | p.Arg90Ile | p.R90I | P03950 | protein_coding | tolerated(0.17) | benign(0.078) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ANG | SNV | Missense_Mutation | novel | c.133N>T | p.Arg45Trp | p.R45W | P03950 | protein_coding | tolerated(0.08) | benign(0.139) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
ANG | SNV | Missense_Mutation | novel | c.103N>G | p.Thr35Ala | p.T35A | P03950 | protein_coding | tolerated(0.75) | benign(0) | TCGA-B5-A1MX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Hormone Therapy | megace | SD |
ANG | SNV | Missense_Mutation | c.19G>A | p.Val7Ile | p.V7I | P03950 | protein_coding | tolerated(0.2) | benign(0.011) | TCGA-BS-A0UM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | |
ANG | SNV | Missense_Mutation | novel | c.323N>T | p.His108Leu | p.H108L | P03950 | protein_coding | tolerated(0.55) | benign(0.012) | TCGA-DD-AAE9-01 | Liver | liver hepatocellular carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
ANG | SNV | Missense_Mutation | novel | c.302N>T | p.Gln101Leu | p.Q101L | P03950 | protein_coding | deleterious(0.03) | possibly_damaging(0.645) | TCGA-77-8154-01 | Lung | lung squamous cell carcinoma | 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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