|
Gene: ARL8B |
Gene summary for ARL8B |
Gene summary. |
Gene information | Species | Human | Gene symbol | ARL8B | Gene ID | 55207 |
Gene name | ADP ribosylation factor like GTPase 8B | |
Gene Alias | ARL10C | |
Cytomap | 3p26.1 | |
Gene Type | protein-coding | GO ID | GO:0001778 | UniProtAcc | A0A024R2D4 |
Top |
Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
55207 | ARL8B | P42T-E | Human | Esophagus | ESCC | 1.11e-16 | 4.99e-01 | 0.1175 |
55207 | ARL8B | P44T-E | Human | Esophagus | ESCC | 3.68e-18 | 8.05e-01 | 0.1096 |
55207 | ARL8B | P47T-E | Human | Esophagus | ESCC | 4.72e-31 | 7.02e-01 | 0.1067 |
55207 | ARL8B | P48T-E | Human | Esophagus | ESCC | 6.41e-12 | 1.32e-01 | 0.0959 |
55207 | ARL8B | P49T-E | Human | Esophagus | ESCC | 1.49e-23 | 2.22e+00 | 0.1768 |
55207 | ARL8B | P52T-E | Human | Esophagus | ESCC | 6.42e-11 | 4.24e-01 | 0.1555 |
55207 | ARL8B | P54T-E | Human | Esophagus | ESCC | 6.44e-06 | 2.66e-01 | 0.0975 |
55207 | ARL8B | P56T-E | Human | Esophagus | ESCC | 2.26e-04 | 7.36e-01 | 0.1613 |
55207 | ARL8B | P57T-E | Human | Esophagus | ESCC | 1.94e-19 | 2.96e-01 | 0.0926 |
55207 | ARL8B | P61T-E | Human | Esophagus | ESCC | 2.97e-11 | 2.39e-01 | 0.099 |
55207 | ARL8B | P62T-E | Human | Esophagus | ESCC | 1.36e-37 | 7.19e-01 | 0.1302 |
55207 | ARL8B | P65T-E | Human | Esophagus | ESCC | 5.52e-17 | 2.25e-01 | 0.0978 |
55207 | ARL8B | P74T-E | Human | Esophagus | ESCC | 1.65e-29 | 8.03e-01 | 0.1479 |
55207 | ARL8B | P75T-E | Human | Esophagus | ESCC | 6.64e-27 | 7.76e-01 | 0.1125 |
55207 | ARL8B | P76T-E | Human | Esophagus | ESCC | 4.08e-08 | 2.40e-01 | 0.1207 |
55207 | ARL8B | P79T-E | Human | Esophagus | ESCC | 1.95e-12 | 2.80e-01 | 0.1154 |
55207 | ARL8B | P80T-E | Human | Esophagus | ESCC | 1.96e-29 | 1.08e+00 | 0.155 |
55207 | ARL8B | P82T-E | Human | Esophagus | ESCC | 2.00e-11 | 8.36e-01 | 0.1072 |
55207 | ARL8B | P83T-E | Human | Esophagus | ESCC | 9.22e-35 | 1.19e+00 | 0.1738 |
55207 | ARL8B | P84T-E | Human | Esophagus | ESCC | 1.72e-03 | 5.76e-01 | 0.0933 |
Page: 1 2 3 4 5 6 7 |
Transcriptomic changes along malignancy continuum. |
∗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. |
Top |
Malignant transformation related pathway analysis |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
Figure of enriched GO biological processes. |
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 |
Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:001603210 | Cervix | CC | viral process | 109/2311 | 415/18723 | 5.40e-15 | 6.46e-12 | 109 |
GO:004206010 | Cervix | CC | wound healing | 109/2311 | 422/18723 | 1.84e-14 | 1.57e-11 | 109 |
GO:001905810 | Cervix | CC | viral life cycle | 87/2311 | 317/18723 | 2.20e-13 | 1.20e-10 | 87 |
GO:005212610 | Cervix | CC | movement in host environment | 52/2311 | 175/18723 | 7.03e-10 | 8.76e-08 | 52 |
GO:005170110 | Cervix | CC | biological process involved in interaction with host | 57/2311 | 203/18723 | 1.18e-09 | 1.41e-07 | 57 |
GO:004440310 | Cervix | CC | biological process involved in symbiotic interaction | 71/2311 | 290/18723 | 7.94e-09 | 6.98e-07 | 71 |
GO:001988210 | Cervix | CC | antigen processing and presentation | 32/2311 | 106/18723 | 8.61e-07 | 3.08e-05 | 32 |
GO:00025048 | Cervix | CC | antigen processing and presentation of peptide or polysaccharide antigen via MHC class II | 16/2311 | 36/18723 | 1.76e-06 | 5.76e-05 | 16 |
GO:00162367 | Cervix | CC | macroautophagy | 58/2311 | 291/18723 | 1.40e-04 | 1.70e-03 | 58 |
GO:00161977 | Cervix | CC | endosomal transport | 48/2311 | 230/18723 | 1.65e-04 | 1.97e-03 | 48 |
GO:00070347 | Cervix | CC | vacuolar transport | 34/2311 | 157/18723 | 7.03e-04 | 6.40e-03 | 34 |
GO:00307057 | Cervix | CC | cytoskeleton-dependent intracellular transport | 40/2311 | 195/18723 | 7.92e-04 | 6.99e-03 | 40 |
GO:00019067 | Cervix | CC | cell killing | 37/2311 | 188/18723 | 2.61e-03 | 1.80e-02 | 37 |
GO:00160506 | Cervix | CC | vesicle organization | 54/2311 | 300/18723 | 2.71e-03 | 1.85e-02 | 54 |
GO:00164827 | Cervix | CC | cytosolic transport | 33/2311 | 168/18723 | 4.43e-03 | 2.70e-02 | 33 |
GO:0002443 | Cervix | CC | leukocyte mediated immunity | 73/2311 | 440/18723 | 5.01e-03 | 2.98e-02 | 73 |
GO:00070416 | Cervix | CC | lysosomal transport | 24/2311 | 114/18723 | 5.81e-03 | 3.33e-02 | 24 |
GO:0006909 | Cervix | CC | phagocytosis | 53/2311 | 308/18723 | 7.49e-03 | 4.01e-02 | 53 |
GO:00070092 | Cervix | CC | plasma membrane organization | 28/2311 | 142/18723 | 7.85e-03 | 4.14e-02 | 28 |
GO:00068873 | Cervix | CC | exocytosis | 59/2311 | 352/18723 | 8.74e-03 | 4.48e-02 | 59 |
Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 |
Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0513220 | Cervix | CC | Salmonella infection | 74/1267 | 249/8465 | 1.33e-09 | 2.54e-08 | 1.50e-08 | 74 |
hsa05132110 | Cervix | CC | Salmonella infection | 74/1267 | 249/8465 | 1.33e-09 | 2.54e-08 | 1.50e-08 | 74 |
hsa05132211 | Esophagus | ESCC | Salmonella infection | 191/4205 | 249/8465 | 6.51e-19 | 5.45e-17 | 2.79e-17 | 191 |
hsa05132310 | Esophagus | ESCC | Salmonella infection | 191/4205 | 249/8465 | 6.51e-19 | 5.45e-17 | 2.79e-17 | 191 |
hsa0513242 | Liver | HCC | Salmonella infection | 178/4020 | 249/8465 | 5.90e-15 | 1.98e-13 | 1.10e-13 | 178 |
hsa0513252 | Liver | HCC | Salmonella infection | 178/4020 | 249/8465 | 5.90e-15 | 1.98e-13 | 1.10e-13 | 178 |
hsa0513216 | Lung | IAC | Salmonella infection | 52/1053 | 249/8465 | 9.46e-05 | 1.28e-03 | 8.50e-04 | 52 |
hsa0513217 | Lung | IAC | Salmonella infection | 52/1053 | 249/8465 | 9.46e-05 | 1.28e-03 | 8.50e-04 | 52 |
hsa0513223 | Lung | AIS | Salmonella infection | 50/961 | 249/8465 | 3.47e-05 | 5.62e-04 | 3.59e-04 | 50 |
hsa0513233 | Lung | AIS | Salmonella infection | 50/961 | 249/8465 | 3.47e-05 | 5.62e-04 | 3.59e-04 | 50 |
hsa0513230 | Oral cavity | OSCC | Salmonella infection | 174/3704 | 249/8465 | 2.67e-17 | 1.49e-15 | 7.58e-16 | 174 |
hsa05132114 | Oral cavity | OSCC | Salmonella infection | 174/3704 | 249/8465 | 2.67e-17 | 1.49e-15 | 7.58e-16 | 174 |
hsa05132210 | Oral cavity | LP | Salmonella infection | 128/2418 | 249/8465 | 1.17e-14 | 2.79e-13 | 1.80e-13 | 128 |
hsa0513238 | Oral cavity | LP | Salmonella infection | 128/2418 | 249/8465 | 1.17e-14 | 2.79e-13 | 1.80e-13 | 128 |
Page: 1 |
Top |
Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
Top |
Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
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. |
Page: 1 |
Top |
Somatic mutation of malignant transformation related genes |
Annotation of somatic variants for genes involved in malignant transformation |
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 |
ARL8B | SNV | Missense_Mutation | c.515N>G | p.Ile172Ser | p.I172S | Q9NVJ2 | protein_coding | tolerated(0.21) | benign(0.031) | TCGA-AN-A0XN-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
ARL8B | SNV | Missense_Mutation | rs766948599 | c.323G>A | p.Arg108Gln | p.R108Q | Q9NVJ2 | protein_coding | tolerated(0.06) | benign(0.006) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR |
ARL8B | SNV | Missense_Mutation | c.344N>C | p.Leu115Pro | p.L115P | Q9NVJ2 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-AA-A01P-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD | |
ARL8B | SNV | Missense_Mutation | rs780847749 | c.460N>A | p.Asp154Asn | p.D154N | Q9NVJ2 | protein_coding | tolerated(0.19) | benign(0.031) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD |
ARL8B | SNV | Missense_Mutation | c.150N>G | p.Ile50Met | p.I50M | Q9NVJ2 | protein_coding | deleterious(0) | probably_damaging(0.946) | TCGA-AZ-6598-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
ARL8B | SNV | Missense_Mutation | novel | c.308N>G | p.Lys103Arg | p.K103R | Q9NVJ2 | protein_coding | tolerated(0.09) | probably_damaging(0.966) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
ARL8B | SNV | Missense_Mutation | rs747994602 | c.193G>A | p.Val65Ile | p.V65I | Q9NVJ2 | protein_coding | deleterious(0.04) | probably_damaging(0.999) | TCGA-F4-6704-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | SD |
ARL8B | SNV | Missense_Mutation | novel | c.538N>T | p.His180Tyr | p.H180Y | Q9NVJ2 | protein_coding | tolerated(0.09) | possibly_damaging(0.855) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ARL8B | SNV | Missense_Mutation | novel | c.398A>G | p.Asp133Gly | p.D133G | Q9NVJ2 | protein_coding | deleterious(0) | probably_damaging(0.97) | TCGA-AP-A1DK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ARL8B | SNV | Missense_Mutation | rs747994602 | c.193G>A | p.Val65Ile | p.V65I | Q9NVJ2 | protein_coding | deleterious(0.04) | probably_damaging(0.999) | TCGA-AX-A06F-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | SD |
Page: 1 2 3 |
Top |
Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
Page: 1 |