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Gene: ARL4A |
Gene summary for ARL4A |
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Gene information | Species | Human | Gene symbol | ARL4A | Gene ID | 10124 |
Gene name | ADP ribosylation factor like GTPase 4A | |
Gene Alias | ARL4 | |
Cytomap | 7p21.3 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | A0A024R9Z2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
10124 | ARL4A | P27T-E | Human | Esophagus | ESCC | 3.63e-37 | 9.23e-01 | 0.1055 |
10124 | ARL4A | P28T-E | Human | Esophagus | ESCC | 1.24e-58 | 1.21e+00 | 0.1149 |
10124 | ARL4A | P30T-E | Human | Esophagus | ESCC | 2.17e-32 | 1.49e+00 | 0.137 |
10124 | ARL4A | P31T-E | Human | Esophagus | ESCC | 9.55e-19 | 4.19e-01 | 0.1251 |
10124 | ARL4A | P32T-E | Human | Esophagus | ESCC | 2.62e-58 | 1.44e+00 | 0.1666 |
10124 | ARL4A | P36T-E | Human | Esophagus | ESCC | 8.92e-08 | 6.97e-01 | 0.1187 |
10124 | ARL4A | P37T-E | Human | Esophagus | ESCC | 3.33e-20 | 5.73e-01 | 0.1371 |
10124 | ARL4A | P38T-E | Human | Esophagus | ESCC | 3.53e-02 | 9.93e-02 | 0.127 |
10124 | ARL4A | P39T-E | Human | Esophagus | ESCC | 1.16e-36 | 1.02e+00 | 0.0894 |
10124 | ARL4A | P40T-E | Human | Esophagus | ESCC | 8.79e-12 | 4.95e-01 | 0.109 |
10124 | ARL4A | P42T-E | Human | Esophagus | ESCC | 1.09e-32 | 1.37e+00 | 0.1175 |
10124 | ARL4A | P44T-E | Human | Esophagus | ESCC | 4.92e-16 | 4.89e-01 | 0.1096 |
10124 | ARL4A | P47T-E | Human | Esophagus | ESCC | 4.11e-36 | 9.91e-01 | 0.1067 |
10124 | ARL4A | P48T-E | Human | Esophagus | ESCC | 2.70e-12 | 3.98e-01 | 0.0959 |
10124 | ARL4A | P49T-E | Human | Esophagus | ESCC | 3.73e-12 | 1.38e+00 | 0.1768 |
10124 | ARL4A | P52T-E | Human | Esophagus | ESCC | 3.66e-35 | 8.52e-01 | 0.1555 |
10124 | ARL4A | P54T-E | Human | Esophagus | ESCC | 7.61e-33 | 9.38e-01 | 0.0975 |
10124 | ARL4A | P56T-E | Human | Esophagus | ESCC | 1.73e-13 | 1.89e+00 | 0.1613 |
10124 | ARL4A | P57T-E | Human | Esophagus | ESCC | 8.23e-21 | 7.16e-01 | 0.0926 |
10124 | ARL4A | P61T-E | Human | Esophagus | ESCC | 8.05e-27 | 8.28e-01 | 0.099 |
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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:00454444 | Breast | Precancer | fat cell differentiation | 26/1080 | 229/18723 | 7.60e-04 | 9.04e-03 | 26 |
GO:004544412 | Breast | IDC | fat cell differentiation | 30/1434 | 229/18723 | 2.72e-03 | 2.41e-02 | 30 |
GO:004544421 | Breast | DCIS | fat cell differentiation | 30/1390 | 229/18723 | 1.70e-03 | 1.68e-02 | 30 |
GO:00454445 | Cervix | CC | fat cell differentiation | 53/2311 | 229/18723 | 3.72e-06 | 9.75e-05 | 53 |
GO:0050873 | Cervix | CC | brown fat cell differentiation | 13/2311 | 50/18723 | 6.42e-03 | 3.58e-02 | 13 |
GO:00454449 | Esophagus | ESCC | fat cell differentiation | 135/8552 | 229/18723 | 3.38e-05 | 2.78e-04 | 135 |
GO:00454442 | Liver | Cirrhotic | fat cell differentiation | 73/4634 | 229/18723 | 8.57e-03 | 3.97e-02 | 73 |
GO:00454441 | Liver | HCC | fat cell differentiation | 120/7958 | 229/18723 | 1.52e-03 | 8.05e-03 | 120 |
GO:00454448 | Oral cavity | OSCC | fat cell differentiation | 120/7305 | 229/18723 | 2.48e-05 | 2.32e-04 | 120 |
GO:004544418 | Thyroid | PTC | fat cell differentiation | 102/5968 | 229/18723 | 3.66e-05 | 3.40e-04 | 102 |
GO:004544423 | Thyroid | ATC | fat cell differentiation | 105/6293 | 229/18723 | 7.42e-05 | 5.62e-04 | 105 |
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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 |
ARL4A | SNV | Missense_Mutation | c.415N>G | p.Arg139Gly | p.R139G | P40617 | protein_coding | tolerated(0.05) | benign(0.383) | TCGA-A2-A1G0-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | SD | |
ARL4A | SNV | Missense_Mutation | novel | c.340G>A | p.Glu114Lys | p.E114K | P40617 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-MA-AA41-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
ARL4A | SNV | Missense_Mutation | novel | c.368A>C | p.Glu123Ala | p.E123A | P40617 | protein_coding | deleterious(0.05) | benign(0.083) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
ARL4A | SNV | Missense_Mutation | novel | c.99G>T | p.Lys33Asn | p.K33N | P40617 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
ARL4A | SNV | Missense_Mutation | novel | c.414G>C | p.Leu138Phe | p.L138F | P40617 | protein_coding | deleterious(0) | probably_damaging(0.961) | TCGA-AJ-A3QS-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | CR |
ARL4A | SNV | Missense_Mutation | rs749392270 | c.316N>A | p.Glu106Lys | p.E106K | P40617 | protein_coding | deleterious(0.01) | probably_damaging(0.918) | TCGA-AJ-A5DW-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ARL4A | SNV | Missense_Mutation | novel | c.104N>T | p.Thr35Ile | p.T35I | P40617 | protein_coding | deleterious(0) | probably_damaging(0.975) | TCGA-AP-A1DO-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ARL4A | SNV | Missense_Mutation | c.71T>C | p.Val24Ala | p.V24A | P40617 | protein_coding | tolerated(0.21) | benign(0.031) | TCGA-AX-A0J0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ARL4A | SNV | Missense_Mutation | novel | c.542A>G | p.Lys181Arg | p.K181R | P40617 | protein_coding | tolerated(0.42) | benign(0.021) | TCGA-BK-A6W3-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ARL4A | SNV | Missense_Mutation | novel | c.377G>A | p.Gly126Glu | p.G126E | P40617 | protein_coding | deleterious(0.03) | probably_damaging(0.993) | TCGA-D1-A1NS-01 | Endometrium | uterine corpus endometrioid carcinoma | 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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