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Gene: SLC7A11 |
Gene summary for SLC7A11 |
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Gene information | Species | Human | Gene symbol | SLC7A11 | Gene ID | 23657 |
Gene name | solute carrier family 7 member 11 | |
Gene Alias | CCBR1 | |
Cytomap | 4q28.3 | |
Gene Type | protein-coding | GO ID | GO:0000096 | UniProtAcc | Q9UPY5 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
23657 | SLC7A11 | LZE2T | Human | Esophagus | ESCC | 6.62e-04 | 4.46e-01 | 0.082 |
23657 | SLC7A11 | LZE4T | Human | Esophagus | ESCC | 2.90e-39 | 1.43e+00 | 0.0811 |
23657 | SLC7A11 | LZE7T | Human | Esophagus | ESCC | 1.08e-14 | 8.50e-01 | 0.0667 |
23657 | SLC7A11 | P4T-E | Human | Esophagus | ESCC | 4.06e-07 | 2.60e-01 | 0.1323 |
23657 | SLC7A11 | P5T-E | Human | Esophagus | ESCC | 5.95e-06 | 1.46e-01 | 0.1327 |
23657 | SLC7A11 | P9T-E | Human | Esophagus | ESCC | 3.53e-24 | 6.74e-01 | 0.1131 |
23657 | SLC7A11 | P15T-E | Human | Esophagus | ESCC | 2.41e-35 | 8.29e-01 | 0.1149 |
23657 | SLC7A11 | P21T-E | Human | Esophagus | ESCC | 3.76e-24 | 6.73e-01 | 0.1617 |
23657 | SLC7A11 | P22T-E | Human | Esophagus | ESCC | 2.11e-06 | 1.71e-01 | 0.1236 |
23657 | SLC7A11 | P23T-E | Human | Esophagus | ESCC | 6.41e-03 | 1.81e-01 | 0.108 |
23657 | SLC7A11 | P26T-E | Human | Esophagus | ESCC | 2.28e-03 | 1.58e-01 | 0.1276 |
23657 | SLC7A11 | P28T-E | Human | Esophagus | ESCC | 7.22e-03 | 2.12e-01 | 0.1149 |
23657 | SLC7A11 | P30T-E | Human | Esophagus | ESCC | 6.64e-38 | 1.34e+00 | 0.137 |
23657 | SLC7A11 | P32T-E | Human | Esophagus | ESCC | 9.98e-39 | 1.23e+00 | 0.1666 |
23657 | SLC7A11 | P39T-E | Human | Esophagus | ESCC | 1.23e-09 | 3.23e-01 | 0.0894 |
23657 | SLC7A11 | P42T-E | Human | Esophagus | ESCC | 2.06e-13 | 7.62e-01 | 0.1175 |
23657 | SLC7A11 | P47T-E | Human | Esophagus | ESCC | 2.45e-02 | 1.31e-01 | 0.1067 |
23657 | SLC7A11 | P48T-E | Human | Esophagus | ESCC | 1.11e-03 | 2.67e-01 | 0.0959 |
23657 | SLC7A11 | P49T-E | Human | Esophagus | ESCC | 5.16e-18 | 2.44e+00 | 0.1768 |
23657 | SLC7A11 | P52T-E | Human | Esophagus | ESCC | 6.67e-12 | 4.06e-01 | 0.1555 |
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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:000963616 | Prostate | BPH | response to toxic substance | 67/3107 | 262/18723 | 1.32e-04 | 1.18e-03 | 67 |
GO:000931414 | Prostate | BPH | response to radiation | 105/3107 | 456/18723 | 2.07e-04 | 1.70e-03 | 105 |
GO:003647317 | Prostate | BPH | cell death in response to oxidative stress | 30/3107 | 95/18723 | 2.29e-04 | 1.83e-03 | 30 |
GO:005087817 | Prostate | BPH | regulation of body fluid levels | 89/3107 | 379/18723 | 3.08e-04 | 2.37e-03 | 89 |
GO:007052716 | Prostate | BPH | platelet aggregation | 23/3107 | 67/18723 | 3.12e-04 | 2.39e-03 | 23 |
GO:19032049 | Prostate | BPH | negative regulation of oxidative stress-induced neuron death | 10/3107 | 19/18723 | 3.36e-04 | 2.52e-03 | 10 |
GO:190040716 | Prostate | BPH | regulation of cellular response to oxidative stress | 28/3107 | 89/18723 | 3.90e-04 | 2.85e-03 | 28 |
GO:190288216 | Prostate | BPH | regulation of response to oxidative stress | 30/3107 | 98/18723 | 4.16e-04 | 3.01e-03 | 30 |
GO:00303237 | Prostate | BPH | respiratory tube development | 48/3107 | 181/18723 | 4.65e-04 | 3.33e-03 | 48 |
GO:00303247 | Prostate | BPH | lung development | 47/3107 | 177/18723 | 5.13e-04 | 3.63e-03 | 47 |
GO:00620127 | Prostate | BPH | regulation of small molecule metabolic process | 79/3107 | 334/18723 | 5.17e-04 | 3.66e-03 | 79 |
GO:19012158 | Prostate | BPH | negative regulation of neuron death | 53/3107 | 208/18723 | 6.87e-04 | 4.58e-03 | 53 |
GO:00517752 | Prostate | BPH | response to redox state | 8/3107 | 15/18723 | 1.21e-03 | 7.41e-03 | 8 |
GO:0050890 | Prostate | BPH | cognition | 69/3107 | 296/18723 | 1.68e-03 | 9.69e-03 | 69 |
GO:00075968 | Prostate | BPH | blood coagulation | 53/3107 | 217/18723 | 1.91e-03 | 1.09e-02 | 53 |
GO:00508178 | Prostate | BPH | coagulation | 54/3107 | 222/18723 | 1.92e-03 | 1.09e-02 | 54 |
GO:00605415 | Prostate | BPH | respiratory system development | 50/3107 | 203/18723 | 2.09e-03 | 1.17e-02 | 50 |
GO:00075998 | Prostate | BPH | hemostasis | 53/3107 | 222/18723 | 3.21e-03 | 1.67e-02 | 53 |
GO:0070306 | Prostate | BPH | lens fiber cell differentiation | 13/3107 | 36/18723 | 3.71e-03 | 1.87e-02 | 13 |
GO:190320210 | Prostate | BPH | negative regulation of oxidative stress-induced cell death | 17/3107 | 53/18723 | 4.11e-03 | 2.04e-02 | 17 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0421629 | Esophagus | ESCC | Ferroptosis | 33/4205 | 41/8465 | 4.58e-05 | 1.99e-04 | 1.02e-04 | 33 |
hsa0421638 | Esophagus | ESCC | Ferroptosis | 33/4205 | 41/8465 | 4.58e-05 | 1.99e-04 | 1.02e-04 | 33 |
hsa0421641 | Liver | HCC | Ferroptosis | 33/4020 | 41/8465 | 1.42e-05 | 9.88e-05 | 5.50e-05 | 33 |
hsa0421651 | Liver | HCC | Ferroptosis | 33/4020 | 41/8465 | 1.42e-05 | 9.88e-05 | 5.50e-05 | 33 |
hsa0421620 | Oral cavity | OSCC | Ferroptosis | 29/3704 | 41/8465 | 4.26e-04 | 1.30e-03 | 6.60e-04 | 29 |
hsa04216110 | Oral cavity | OSCC | Ferroptosis | 29/3704 | 41/8465 | 4.26e-04 | 1.30e-03 | 6.60e-04 | 29 |
hsa0421626 | Prostate | Tumor | Ferroptosis | 24/1791 | 41/8465 | 1.94e-07 | 2.14e-06 | 1.33e-06 | 24 |
hsa0421636 | Prostate | Tumor | Ferroptosis | 24/1791 | 41/8465 | 1.94e-07 | 2.14e-06 | 1.33e-06 | 24 |
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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 |
SLC7A11 | SNV | Missense_Mutation | novel | c.1412A>G | p.Asp471Gly | p.D471G | Q9UPY5 | protein_coding | tolerated(0.34) | benign(0.005) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
SLC7A11 | SNV | Missense_Mutation | novel | c.1483N>A | p.Val495Ile | p.V495I | Q9UPY5 | protein_coding | tolerated(0.29) | benign(0.018) | TCGA-C8-A8HP-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | 5-fluorouracil | CR |
SLC7A11 | SNV | Missense_Mutation | novel | c.538N>C | p.Asn180His | p.N180H | Q9UPY5 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-D8-A1Y3-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicine+cyclophosphamide | SD |
SLC7A11 | SNV | Missense_Mutation | novel | c.197C>T | p.Pro66Leu | p.P66L | Q9UPY5 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-C5-A7X5-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | carboplatin | PD |
SLC7A11 | SNV | Missense_Mutation | c.787N>A | p.Glu263Lys | p.E263K | Q9UPY5 | protein_coding | tolerated(0.1) | benign(0.101) | TCGA-LP-A5U2-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Unknown | Unknown | SD | |
SLC7A11 | SNV | Missense_Mutation | rs760898836 | c.959N>T | p.Pro320Leu | p.P320L | Q9UPY5 | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-VS-A94Z-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
SLC7A11 | SNV | Missense_Mutation | novel | c.854N>T | p.Asn285Ile | p.N285I | Q9UPY5 | protein_coding | deleterious(0.02) | probably_damaging(0.996) | TCGA-A6-3808-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
SLC7A11 | SNV | Missense_Mutation | c.802N>A | p.Leu268Ile | p.L268I | Q9UPY5 | protein_coding | deleterious(0.01) | possibly_damaging(0.53) | TCGA-AD-5900-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
SLC7A11 | SNV | Missense_Mutation | c.167C>T | p.Thr56Ile | p.T56I | Q9UPY5 | protein_coding | deleterious(0.02) | benign(0.085) | TCGA-AZ-6599-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
SLC7A11 | SNV | Missense_Mutation | novel | c.941N>C | p.Asn314Thr | p.N314T | Q9UPY5 | protein_coding | tolerated(0.73) | benign(0.027) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
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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 |
23657 | SLC7A11 | TRANSPORTER, DRUGGABLE GENOME, CELL SURFACE | RILUZOLE | RILUZOLE | ||
23657 | SLC7A11 | TRANSPORTER, DRUGGABLE GENOME, CELL SURFACE | inhibitor | 135650876 | QUISQUALATE |
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