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Gene: MRPL37 |
Gene summary for MRPL37 |
| Gene information | Species | Human | Gene symbol | MRPL37 | Gene ID | 51253 |
| Gene name | mitochondrial ribosomal protein L37 | |
| Gene Alias | L2mt | |
| Cytomap | 1p32.3 | |
| Gene Type | protein-coding | GO ID | GO:0006412 | UniProtAcc | S4R369 |
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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 |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 51253 | MRPL37 | HTA11_10711_2000001011 | Human | Colorectum | AD | 2.45e-04 | 4.03e-01 | 0.0338 |
| 51253 | MRPL37 | HTA11_7696_3000711011 | Human | Colorectum | AD | 2.10e-25 | 6.83e-01 | 0.0674 |
| 51253 | MRPL37 | HTA11_7469_2000001011 | Human | Colorectum | AD | 2.35e-03 | 6.16e-01 | -0.0124 |
| 51253 | MRPL37 | HTA11_6818_2000001021 | Human | Colorectum | AD | 4.32e-03 | 3.29e-01 | 0.0588 |
| 51253 | MRPL37 | HTA11_99999970781_79442 | Human | Colorectum | MSS | 2.01e-25 | 7.73e-01 | 0.294 |
| 51253 | MRPL37 | HTA11_99999965104_69814 | Human | Colorectum | MSS | 1.41e-20 | 8.39e-01 | 0.281 |
| 51253 | MRPL37 | HTA11_99999971662_82457 | Human | Colorectum | MSS | 7.15e-25 | 8.44e-01 | 0.3859 |
| 51253 | MRPL37 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 3.57e-04 | 2.54e-01 | 0.3005 |
| 51253 | MRPL37 | LZE2T | Human | Esophagus | ESCC | 1.92e-05 | 5.62e-01 | 0.082 |
| 51253 | MRPL37 | LZE4T | Human | Esophagus | ESCC | 1.53e-08 | 4.18e-01 | 0.0811 |
| 51253 | MRPL37 | LZE7T | Human | Esophagus | ESCC | 2.12e-09 | 8.56e-01 | 0.0667 |
| 51253 | MRPL37 | LZE8T | Human | Esophagus | ESCC | 1.54e-06 | 5.16e-01 | 0.067 |
| 51253 | MRPL37 | LZE20T | Human | Esophagus | ESCC | 6.73e-06 | 3.51e-01 | 0.0662 |
| 51253 | MRPL37 | LZE24T | Human | Esophagus | ESCC | 2.56e-28 | 9.93e-01 | 0.0596 |
| 51253 | MRPL37 | LZE6T | Human | Esophagus | ESCC | 4.63e-12 | 6.91e-01 | 0.0845 |
| 51253 | MRPL37 | P1T-E | Human | Esophagus | ESCC | 2.48e-09 | 6.01e-01 | 0.0875 |
| 51253 | MRPL37 | P2T-E | Human | Esophagus | ESCC | 2.52e-50 | 1.02e+00 | 0.1177 |
| 51253 | MRPL37 | P4T-E | Human | Esophagus | ESCC | 1.34e-40 | 1.16e+00 | 0.1323 |
| 51253 | MRPL37 | P5T-E | Human | Esophagus | ESCC | 1.60e-33 | 8.62e-01 | 0.1327 |
| 51253 | MRPL37 | P8T-E | Human | Esophagus | ESCC | 5.33e-21 | 5.60e-01 | 0.0889 |
| Page: 1 2 3 4 5 6 7 8 |
| ∗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 |
| 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 |
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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 |
| MRPL37 | SNV | Missense_Mutation | rs768836635 | c.110N>T | p.Ser37Phe | p.S37F | protein_coding | deleterious_low_confidence(0) | probably_damaging(0.956) | TCGA-BH-A0HF-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD | |
| MRPL37 | insertion | Nonsense_Mutation | novel | c.961_962insGTCATGGCTGAAAAGAACAAGTACTAAACTTTGATTCTCAGCA | p.Ala321GlyfsTer4 | p.A321Gfs*4 | protein_coding | TCGA-A8-A09N-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |||
| MRPL37 | insertion | Nonsense_Mutation | novel | c.1164_1165insTGTAAAGGGAAGAACTAGAAG | p.Cys388_Leu389insCysLysGlyLysAsnTerLys | p.C388_L389insCKGKN*K | protein_coding | TCGA-AN-A0FS-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |||
| MRPL37 | SNV | Missense_Mutation | novel | c.832G>A | p.Gly278Arg | p.G278R | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
| MRPL37 | SNV | Missense_Mutation | novel | c.1379G>A | p.Arg460His | p.R460H | protein_coding | deleterious_low_confidence(0) | benign(0) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
| MRPL37 | SNV | Missense_Mutation | rs369065705 | c.1033G>A | p.Val345Met | p.V345M | protein_coding | deleterious(0.05) | benign(0.115) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
| MRPL37 | SNV | Missense_Mutation | c.349G>A | p.Val117Ile | p.V117I | protein_coding | tolerated(0.11) | benign(0.373) | TCGA-CM-4746-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | ||
| MRPL37 | SNV | Missense_Mutation | rs753105572 | c.1040C>T | p.Thr347Met | p.T347M | protein_coding | deleterious(0.05) | probably_damaging(0.959) | TCGA-AG-A02N-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | Chemotherapy | folinic | CR | |
| MRPL37 | SNV | Missense_Mutation | novel | c.892N>C | p.Asn298His | p.N298H | protein_coding | deleterious(0) | benign(0.046) | TCGA-AG-A032-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | III/IV | Targeted Molecular therapy | bevacizumab | PD | |
| MRPL37 | insertion | Frame_Shift_Ins | novel | c.1181dupA | p.Arg395GlufsTer7 | p.R395Efs*7 | protein_coding | TCGA-AA-3710-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
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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 |