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Gene: RAB23 |
Gene summary for RAB23 |
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Gene information | Species | Human | Gene symbol | RAB23 | Gene ID | 51715 |
Gene name | RAB23, member RAS oncogene family | |
Gene Alias | HSPC137 | |
Cytomap | 6p12.1-p11.2 | |
Gene Type | protein-coding | GO ID | GO:0000045 | UniProtAcc | A0A024RD41 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
51715 | RAB23 | LZE24T | Human | Esophagus | ESCC | 1.95e-10 | 2.24e-01 | 0.0596 |
51715 | RAB23 | P2T-E | Human | Esophagus | ESCC | 1.64e-07 | 8.23e-02 | 0.1177 |
51715 | RAB23 | P4T-E | Human | Esophagus | ESCC | 4.01e-11 | 2.68e-01 | 0.1323 |
51715 | RAB23 | P5T-E | Human | Esophagus | ESCC | 5.31e-05 | 8.15e-02 | 0.1327 |
51715 | RAB23 | P8T-E | Human | Esophagus | ESCC | 3.37e-04 | 7.07e-02 | 0.0889 |
51715 | RAB23 | P9T-E | Human | Esophagus | ESCC | 2.30e-04 | 1.54e-01 | 0.1131 |
51715 | RAB23 | P10T-E | Human | Esophagus | ESCC | 6.11e-08 | 1.49e-01 | 0.116 |
51715 | RAB23 | P11T-E | Human | Esophagus | ESCC | 1.49e-05 | 2.73e-01 | 0.1426 |
51715 | RAB23 | P12T-E | Human | Esophagus | ESCC | 2.05e-20 | 3.15e-01 | 0.1122 |
51715 | RAB23 | P15T-E | Human | Esophagus | ESCC | 1.05e-08 | 1.51e-01 | 0.1149 |
51715 | RAB23 | P16T-E | Human | Esophagus | ESCC | 8.82e-09 | 1.48e-01 | 0.1153 |
51715 | RAB23 | P17T-E | Human | Esophagus | ESCC | 3.65e-03 | 1.87e-01 | 0.1278 |
51715 | RAB23 | P21T-E | Human | Esophagus | ESCC | 4.74e-03 | 5.00e-02 | 0.1617 |
51715 | RAB23 | P22T-E | Human | Esophagus | ESCC | 1.92e-02 | 6.26e-02 | 0.1236 |
51715 | RAB23 | P23T-E | Human | Esophagus | ESCC | 1.88e-06 | 1.93e-01 | 0.108 |
51715 | RAB23 | P24T-E | Human | Esophagus | ESCC | 1.21e-09 | 1.24e-01 | 0.1287 |
51715 | RAB23 | P26T-E | Human | Esophagus | ESCC | 6.14e-11 | 2.58e-01 | 0.1276 |
51715 | RAB23 | P27T-E | Human | Esophagus | ESCC | 6.47e-12 | 2.25e-01 | 0.1055 |
51715 | RAB23 | P28T-E | Human | Esophagus | ESCC | 1.89e-07 | 1.16e-01 | 0.1149 |
51715 | RAB23 | P31T-E | Human | Esophagus | ESCC | 5.84e-15 | 1.07e-01 | 0.1251 |
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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:0072594110 | Esophagus | ESCC | establishment of protein localization to organelle | 311/8552 | 422/18723 | 3.02e-32 | 2.13e-29 | 311 |
GO:0006913110 | Esophagus | ESCC | nucleocytoplasmic transport | 230/8552 | 301/18723 | 6.04e-28 | 2.02e-25 | 230 |
GO:0051169110 | Esophagus | ESCC | nuclear transport | 230/8552 | 301/18723 | 6.04e-28 | 2.02e-25 | 230 |
GO:001623617 | Esophagus | ESCC | macroautophagy | 216/8552 | 291/18723 | 1.94e-23 | 4.57e-21 | 216 |
GO:003238618 | Esophagus | ESCC | regulation of intracellular transport | 243/8552 | 337/18723 | 3.20e-23 | 7.25e-21 | 243 |
GO:003450418 | Esophagus | ESCC | protein localization to nucleus | 211/8552 | 290/18723 | 4.06e-21 | 6.60e-19 | 211 |
GO:0033157110 | Esophagus | ESCC | regulation of intracellular protein transport | 169/8552 | 229/18723 | 3.31e-18 | 3.23e-16 | 169 |
GO:0046822110 | Esophagus | ESCC | regulation of nucleocytoplasmic transport | 88/8552 | 106/18723 | 1.88e-15 | 1.19e-13 | 88 |
GO:001703818 | Esophagus | ESCC | protein import | 149/8552 | 206/18723 | 5.90e-15 | 3.31e-13 | 149 |
GO:190018018 | Esophagus | ESCC | regulation of protein localization to nucleus | 102/8552 | 136/18723 | 2.84e-12 | 1.13e-10 | 102 |
GO:000703314 | Esophagus | ESCC | vacuole organization | 127/8552 | 180/18723 | 1.04e-11 | 3.85e-10 | 127 |
GO:005117014 | Esophagus | ESCC | import into nucleus | 111/8552 | 159/18723 | 5.69e-10 | 1.44e-08 | 111 |
GO:000660613 | Esophagus | ESCC | protein import into nucleus | 108/8552 | 155/18723 | 1.16e-09 | 2.77e-08 | 108 |
GO:0006753110 | Esophagus | ESCC | nucleoside phosphate metabolic process | 288/8552 | 497/18723 | 1.80e-08 | 3.50e-07 | 288 |
GO:0019693111 | Esophagus | ESCC | ribose phosphate metabolic process | 234/8552 | 396/18723 | 4.24e-08 | 7.76e-07 | 234 |
GO:0009117111 | Esophagus | ESCC | nucleotide metabolic process | 282/8552 | 489/18723 | 4.70e-08 | 8.50e-07 | 282 |
GO:190503712 | Esophagus | ESCC | autophagosome organization | 73/8552 | 103/18723 | 1.88e-07 | 2.93e-06 | 73 |
GO:190458914 | Esophagus | ESCC | regulation of protein import | 49/8552 | 63/18723 | 1.91e-07 | 2.97e-06 | 49 |
GO:0009141111 | Esophagus | ESCC | nucleoside triphosphate metabolic process | 78/8552 | 112/18723 | 2.36e-07 | 3.59e-06 | 78 |
GO:0009259111 | Esophagus | ESCC | ribonucleotide metabolic process | 224/8552 | 385/18723 | 4.41e-07 | 6.00e-06 | 224 |
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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 |
RAB23 | SNV | Missense_Mutation | c.269N>G | p.Ser90Cys | p.S90C | Q9ULC3 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
RAB23 | SNV | Missense_Mutation | c.128G>A | p.Gly43Glu | p.G43E | Q9ULC3 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
RAB23 | SNV | Missense_Mutation | c.422N>C | p.Lys141Thr | p.K141T | Q9ULC3 | protein_coding | deleterious(0.03) | possibly_damaging(0.447) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR | |
RAB23 | SNV | Missense_Mutation | novel | c.109N>T | p.Asp37Tyr | p.D37Y | Q9ULC3 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
RAB23 | SNV | Missense_Mutation | c.422N>C | p.Lys141Thr | p.K141T | Q9ULC3 | protein_coding | deleterious(0.03) | possibly_damaging(0.447) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
RAB23 | SNV | Missense_Mutation | novel | c.18G>A | p.Met6Ile | p.M6I | Q9ULC3 | protein_coding | tolerated(0.37) | benign(0) | TCGA-AJ-A23O-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
RAB23 | SNV | Missense_Mutation | rs145669565 | c.239N>A | p.Arg80Gln | p.R80Q | Q9ULC3 | protein_coding | deleterious(0.01) | probably_damaging(0.985) | TCGA-AP-A056-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
RAB23 | SNV | Missense_Mutation | c.328N>A | p.Glu110Lys | p.E110K | Q9ULC3 | protein_coding | deleterious(0) | probably_damaging(0.993) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD | |
RAB23 | SNV | Missense_Mutation | novel | c.446G>T | p.Arg149Ile | p.R149I | Q9ULC3 | protein_coding | deleterious(0) | probably_damaging(0.987) | TCGA-B5-A1MX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Hormone Therapy | megace | SD |
RAB23 | SNV | Missense_Mutation | rs150655349 | c.25G>A | p.Ala9Thr | p.A9T | Q9ULC3 | protein_coding | tolerated(0.32) | benign(0.263) | TCGA-BK-A13B-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
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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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