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Gene: LCORL |
Gene summary for LCORL |
 Gene summary. |
| 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 |
| 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 |
| 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 |
| Page: 1 2 3 4 5 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Colorectum (GSE201348) |  | FAP: Familial adenomatous polyposis |
| CRC: Colorectal cancer | ||
| Colorectum (HTA11) |  | AD: Adenomas |
| SER: Sessile serrated lesions | ||
| MSI-H: Microsatellite-high colorectal cancer | ||
| MSS: Microsatellite stable colorectal cancer | ||
| Liver |  | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease | ||
| Lung |  | AAH: Atypical adenomatous hyperplasia |
| AIS: Adenocarcinoma in situ | ||
| IAC: Invasive lung adenocarcinoma | ||
| MIA: Minimally invasive adenocarcinoma | ||
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia | ||
| NEOLP: Non-erosive oral lichen planus | ||
| OSCC: Oral squamous cell carcinoma | ||
| Thyroid |  | ATC: Anaplastic thyroid cancer |
| HT: Hashimoto's thyroiditis | ||
| PTC: Papillary thyroid cancer |
| ∗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 |
| 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 |
| Page: 1 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| Page: 1 |
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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 |
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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 |
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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 |
| LCORL | SNV | Missense_Mutation | novel | c.4658N>C | p.Arg1553Thr | p.R1553T | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-AC-A5XS-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | femara | SD | |
| LCORL | SNV | Missense_Mutation | novel | c.4462N>A | p.Glu1488Lys | p.E1488K | protein_coding | deleterious(0.02) | probably_damaging(0.922) | TCGA-AC-A5XS-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | femara | SD | |
| LCORL | SNV | Missense_Mutation | c.1535G>A | p.Ser512Asn | p.S512N | Q8N3X6 | protein_coding | tolerated(0.98) | benign(0) | TCGA-E9-A1N9-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD | |
| LCORL | SNV | Missense_Mutation | novel | c.4459N>T | p.Leu1487Phe | p.L1487F | protein_coding | tolerated(0.16) | benign(0.182) | TCGA-EW-A6SA-01 | Breast | breast invasive carcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
| LCORL | insertion | Frame_Shift_Ins | novel | c.456_457insGTAGGACTGAGTC | p.Ile153ValfsTer23 | p.I153Vfs*23 | Q8N3X6 | protein_coding | TCGA-AO-A0JJ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophospamide | SD | ||
| LCORL | insertion | Frame_Shift_Ins | novel | c.1506_1507insTTTTCAGTTTTTGGAGAGCTGATCCTTCTAGG | p.Thr503PhefsTer16 | p.T503Ffs*16 | Q8N3X6 | protein_coding | TCGA-BH-A0HQ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | arimidex | SD | ||
| LCORL | SNV | Missense_Mutation | c.1769N>T | p.Ser590Leu | p.S590L | Q8N3X6 | protein_coding | deleterious_low_confidence(0) | possibly_damaging(0.598) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
| LCORL | SNV | Missense_Mutation | novel | c.1298T>C | p.Leu433Ser | p.L433S | Q8N3X6 | protein_coding | tolerated(0.25) | benign(0.398) | TCGA-MA-AA42-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD |
| LCORL | SNV | Missense_Mutation | rs765209311 | c.1253G>A | p.Arg418Gln | p.R418Q | Q8N3X6 | protein_coding | deleterious(0) | possibly_damaging(0.795) | TCGA-PN-A8MA-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | SD |
| LCORL | SNV | Missense_Mutation | novel | c.4137N>C | p.Lys1379Asn | p.K1379N | protein_coding | tolerated(1) | benign(0.048) | TCGA-VS-A957-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| Page: 1 2 3 4 5 6 7 8 9 |
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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 |
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