![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: SLC43A3 |
Gene summary for SLC43A3 |
![]() |
Gene information | Species | Human | Gene symbol | SLC43A3 | Gene ID | 29015 |
Gene name | solute carrier family 43 member 3 | |
Gene Alias | EEG1 | |
Cytomap | 11q12.1 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | A0A024R4Y2 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
29015 | SLC43A3 | LZE22T | Human | Esophagus | ESCC | 2.49e-02 | 1.28e-01 | 0.068 |
29015 | SLC43A3 | P2T-E | Human | Esophagus | ESCC | 3.57e-22 | 2.28e-01 | 0.1177 |
29015 | SLC43A3 | P4T-E | Human | Esophagus | ESCC | 1.60e-10 | 3.19e-01 | 0.1323 |
29015 | SLC43A3 | P8T-E | Human | Esophagus | ESCC | 5.45e-04 | 7.20e-02 | 0.0889 |
29015 | SLC43A3 | P9T-E | Human | Esophagus | ESCC | 1.27e-04 | -3.68e-02 | 0.1131 |
29015 | SLC43A3 | P10T-E | Human | Esophagus | ESCC | 2.42e-09 | 1.52e-01 | 0.116 |
29015 | SLC43A3 | P11T-E | Human | Esophagus | ESCC | 2.69e-06 | 3.14e-01 | 0.1426 |
29015 | SLC43A3 | P12T-E | Human | Esophagus | ESCC | 1.13e-03 | -7.27e-02 | 0.1122 |
29015 | SLC43A3 | P16T-E | Human | Esophagus | ESCC | 6.30e-05 | 9.56e-02 | 0.1153 |
29015 | SLC43A3 | P17T-E | Human | Esophagus | ESCC | 3.25e-07 | 5.96e-01 | 0.1278 |
29015 | SLC43A3 | P19T-E | Human | Esophagus | ESCC | 2.54e-03 | 2.83e-01 | 0.1662 |
29015 | SLC43A3 | P20T-E | Human | Esophagus | ESCC | 2.33e-13 | 1.56e-01 | 0.1124 |
29015 | SLC43A3 | P21T-E | Human | Esophagus | ESCC | 1.70e-21 | 5.70e-01 | 0.1617 |
29015 | SLC43A3 | P23T-E | Human | Esophagus | ESCC | 4.30e-02 | -1.80e-02 | 0.108 |
29015 | SLC43A3 | P24T-E | Human | Esophagus | ESCC | 1.83e-09 | 1.03e-01 | 0.1287 |
29015 | SLC43A3 | P27T-E | Human | Esophagus | ESCC | 3.89e-03 | -1.38e-02 | 0.1055 |
29015 | SLC43A3 | P31T-E | Human | Esophagus | ESCC | 1.29e-16 | 4.36e-01 | 0.1251 |
29015 | SLC43A3 | P32T-E | Human | Esophagus | ESCC | 3.60e-03 | -2.48e-02 | 0.1666 |
29015 | SLC43A3 | P36T-E | Human | Esophagus | ESCC | 2.23e-05 | 4.66e-01 | 0.1187 |
29015 | SLC43A3 | P37T-E | Human | Esophagus | ESCC | 3.67e-11 | 4.46e-01 | 0.1371 |
Page: 1 2 3 4 |
![]() |
∗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 |
![]() |
![]() |
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 |
![]() |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
Page: 1 |
![]() |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
Page: 1 |
Top |
Cell-cell communication analysis |
![]() |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
Top |
Single-cell gene regulatory network inference analysis |
![]() |
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 |
![]() |
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 |
SLC43A3 | SNV | Missense_Mutation | c.712C>A | p.Leu238Met | p.L238M | Q8NBI5 | protein_coding | tolerated(0.06) | possibly_damaging(0.472) | TCGA-A6-2686-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
SLC43A3 | SNV | Missense_Mutation | novel | c.38N>C | p.Leu13Pro | p.L13P | Q8NBI5 | protein_coding | deleterious(0) | probably_damaging(0.983) | TCGA-AA-3715-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
SLC43A3 | SNV | Missense_Mutation | rs188327992 | c.647G>A | p.Arg216His | p.R216H | Q8NBI5 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-AA-3811-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD |
SLC43A3 | SNV | Missense_Mutation | rs140882001 | c.340C>T | p.Arg114Cys | p.R114C | Q8NBI5 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
SLC43A3 | SNV | Missense_Mutation | rs375906198 | c.370N>A | p.Ala124Thr | p.A124T | Q8NBI5 | protein_coding | deleterious(0.01) | possibly_damaging(0.76) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR |
SLC43A3 | SNV | Missense_Mutation | rs375844954 | c.320G>A | p.Arg107Gln | p.R107Q | Q8NBI5 | protein_coding | deleterious(0.01) | probably_damaging(0.99) | TCGA-AD-6901-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Chemotherapy | xeloda | PD |
SLC43A3 | SNV | Missense_Mutation | rs188327992 | c.647G>A | p.Arg216His | p.R216H | Q8NBI5 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-AZ-4615-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | xeloda | PD |
SLC43A3 | SNV | Missense_Mutation | rs371491685 | c.341N>A | p.Arg114His | p.R114H | Q8NBI5 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-G4-6302-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
SLC43A3 | SNV | Missense_Mutation | rs375906198 | c.370G>A | p.Ala124Thr | p.A124T | Q8NBI5 | protein_coding | deleterious(0.01) | possibly_damaging(0.76) | TCGA-G4-6628-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
SLC43A3 | SNV | Missense_Mutation | rs201915801 | c.646N>T | p.Arg216Cys | p.R216C | Q8NBI5 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-AG-3896-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
Page: 1 2 3 4 5 6 |
Top |
Related drugs of malignant transformation related genes |
![]() |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
Page: 1 |