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Gene: LCORL |
Gene summary for LCORL |
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Gene information | Species | Human | Gene symbol | LCORL | Gene ID | 254251 |
Gene name | ligand dependent nuclear receptor corepressor like | |
Gene Alias | MLR1 | |
Cytomap | 4p15.31 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q8N3X6 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
254251 | LCORL | HTA11_3410_2000001011 | Human | Colorectum | AD | 5.51e-17 | -6.42e-01 | 0.0155 |
254251 | LCORL | HTA11_2487_2000001011 | Human | Colorectum | SER | 7.32e-04 | -4.76e-01 | -0.1808 |
254251 | LCORL | HTA11_3361_2000001011 | Human | Colorectum | AD | 1.09e-03 | -5.06e-01 | -0.1207 |
254251 | LCORL | HTA11_83_2000001011 | Human | Colorectum | SER | 5.55e-03 | -4.54e-01 | -0.1526 |
254251 | LCORL | HTA11_696_2000001011 | Human | Colorectum | AD | 5.99e-11 | -4.14e-01 | -0.1464 |
254251 | LCORL | HTA11_866_3004761011 | Human | Colorectum | AD | 4.52e-12 | -5.98e-01 | 0.096 |
254251 | LCORL | HTA11_8622_2000001021 | Human | Colorectum | SER | 4.33e-03 | -5.69e-01 | 0.0528 |
254251 | LCORL | HTA11_10711_2000001011 | Human | Colorectum | AD | 2.19e-02 | -4.93e-01 | 0.0338 |
254251 | LCORL | HTA11_7696_3000711011 | Human | Colorectum | AD | 1.32e-20 | -5.24e-01 | 0.0674 |
254251 | LCORL | HTA11_6818_2000001021 | Human | Colorectum | AD | 7.34e-04 | -6.09e-01 | 0.0588 |
254251 | LCORL | HTA11_99999970781_79442 | Human | Colorectum | MSS | 7.83e-11 | -4.47e-01 | 0.294 |
254251 | LCORL | HTA11_99999971662_82457 | Human | Colorectum | MSS | 3.95e-16 | -5.15e-01 | 0.3859 |
254251 | LCORL | HTA11_99999973899_84307 | Human | Colorectum | MSS | 2.68e-09 | -7.69e-01 | 0.2585 |
254251 | LCORL | HTA11_99999974143_84620 | Human | Colorectum | MSS | 4.74e-22 | -6.24e-01 | 0.3005 |
254251 | LCORL | A001-C-207 | Human | Colorectum | FAP | 1.00e-05 | -4.04e-01 | 0.1278 |
254251 | LCORL | A015-C-203 | Human | Colorectum | FAP | 2.95e-36 | -5.99e-01 | -0.1294 |
254251 | LCORL | A015-C-204 | Human | Colorectum | FAP | 6.96e-07 | -4.21e-01 | -0.0228 |
254251 | LCORL | A014-C-040 | Human | Colorectum | FAP | 8.21e-05 | -3.88e-01 | -0.1184 |
254251 | LCORL | A002-C-201 | Human | Colorectum | FAP | 7.88e-17 | -4.54e-01 | 0.0324 |
254251 | LCORL | A002-C-203 | Human | Colorectum | FAP | 7.62e-05 | -2.77e-01 | 0.2786 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
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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 |
LCORL | SNV | Missense_Mutation | rs779332214 | c.656G>A | p.Arg219Gln | p.R219Q | Q8N3X6 | protein_coding | deleterious(0.01) | probably_damaging(0.988) | TCGA-BS-A0UF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
LCORL | SNV | Missense_Mutation | c.1237A>G | p.Lys413Glu | p.K413E | Q8N3X6 | protein_coding | deleterious(0.01) | benign(0.068) | TCGA-D1-A15X-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
LCORL | SNV | Missense_Mutation | c.1400C>A | p.Ser467Tyr | p.S467Y | Q8N3X6 | protein_coding | deleterious(0.03) | benign(0.101) | TCGA-D1-A17Q-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
LCORL | SNV | Missense_Mutation | c.506C>T | p.Ala169Val | p.A169V | Q8N3X6 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-D1-A17Q-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
LCORL | SNV | Missense_Mutation | novel | c.5528N>G | p.Glu1843Gly | p.E1843G | protein_coding | deleterious(0.01) | possibly_damaging(0.863) | TCGA-DI-A1BU-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | paclitaxel | SD | |
LCORL | SNV | Missense_Mutation | novel | c.3485N>G | p.Asn1162Ser | p.N1162S | protein_coding | deleterious(0.04) | benign(0.4) | TCGA-DI-A1BU-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | paclitaxel | SD | |
LCORL | SNV | Missense_Mutation | novel | c.4540G>A | p.Glu1514Lys | p.E1514K | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-DI-A2QY-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | paclitaxel | CR | |
LCORL | SNV | Missense_Mutation | novel | c.3503C>T | p.Ser1168Phe | p.S1168F | protein_coding | deleterious(0.02) | probably_damaging(0.999) | TCGA-E6-A1LX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
LCORL | SNV | Missense_Mutation | novel | c.700C>A | p.Leu234Ile | p.L234I | Q8N3X6 | protein_coding | deleterious(0) | probably_damaging(0.987) | TCGA-E6-A1LX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
LCORL | SNV | Missense_Mutation | novel | c.4768G>T | p.Ala1590Ser | p.A1590S | protein_coding | tolerated(0.23) | benign(0.173) | TCGA-E6-A1M0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | 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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