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Gene: R3HCC1L |
Gene summary for R3HCC1L |
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Gene information | Species | Human | Gene symbol | R3HCC1L | Gene ID | 27291 |
Gene name | R3H domain and coiled-coil containing 1 like | |
Gene Alias | C10orf28 | |
Cytomap | 10q24.2 | |
Gene Type | protein-coding | GO ID | GO:0003674 | UniProtAcc | D3DR60 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
27291 | R3HCC1L | HTA11_3410_2000001011 | Human | Colorectum | AD | 1.99e-09 | -4.81e-01 | 0.0155 |
27291 | R3HCC1L | HTA11_696_2000001011 | Human | Colorectum | AD | 3.86e-06 | -3.30e-01 | -0.1464 |
27291 | R3HCC1L | HTA11_866_3004761011 | Human | Colorectum | AD | 1.62e-06 | -4.41e-01 | 0.096 |
27291 | R3HCC1L | HTA11_10711_2000001011 | Human | Colorectum | AD | 7.56e-03 | -4.32e-01 | 0.0338 |
27291 | R3HCC1L | HTA11_7696_3000711011 | Human | Colorectum | AD | 1.85e-11 | -4.22e-01 | 0.0674 |
27291 | R3HCC1L | HTA11_99999970781_79442 | Human | Colorectum | MSS | 3.10e-12 | -4.32e-01 | 0.294 |
27291 | R3HCC1L | HTA11_99999971662_82457 | Human | Colorectum | MSS | 7.87e-06 | -3.81e-01 | 0.3859 |
27291 | R3HCC1L | HTA11_99999973899_84307 | Human | Colorectum | MSS | 1.94e-02 | -4.99e-01 | 0.2585 |
27291 | R3HCC1L | HTA11_99999974143_84620 | Human | Colorectum | MSS | 2.04e-12 | -4.79e-01 | 0.3005 |
27291 | R3HCC1L | A002-C-010 | Human | Colorectum | FAP | 8.31e-03 | -1.05e-01 | 0.242 |
27291 | R3HCC1L | A015-C-203 | Human | Colorectum | FAP | 6.84e-18 | -3.55e-01 | -0.1294 |
27291 | R3HCC1L | A015-C-204 | Human | Colorectum | FAP | 1.75e-05 | -3.18e-01 | -0.0228 |
27291 | R3HCC1L | A014-C-040 | Human | Colorectum | FAP | 2.62e-02 | -3.60e-01 | -0.1184 |
27291 | R3HCC1L | A002-C-201 | Human | Colorectum | FAP | 6.54e-09 | -2.47e-01 | 0.0324 |
27291 | R3HCC1L | A002-C-203 | Human | Colorectum | FAP | 8.24e-04 | -1.08e-01 | 0.2786 |
27291 | R3HCC1L | A001-C-119 | Human | Colorectum | FAP | 3.54e-12 | -5.54e-01 | -0.1557 |
27291 | R3HCC1L | A001-C-108 | Human | Colorectum | FAP | 1.80e-10 | -2.74e-01 | -0.0272 |
27291 | R3HCC1L | A002-C-205 | Human | Colorectum | FAP | 4.97e-18 | -4.19e-01 | -0.1236 |
27291 | R3HCC1L | A001-C-104 | Human | Colorectum | FAP | 1.50e-04 | -2.78e-01 | 0.0184 |
27291 | R3HCC1L | A015-C-005 | Human | Colorectum | FAP | 3.24e-03 | -2.14e-01 | -0.0336 |
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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 |
Page: 1 |
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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 |
R3HCC1L | SNV | Missense_Mutation | rs369451185 | c.1447N>C | p.Tyr483His | p.Y483H | protein_coding | tolerated(0.16) | benign(0.013) | TCGA-A8-A09Z-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
R3HCC1L | SNV | Missense_Mutation | novel | c.859N>A | p.Glu287Lys | p.E287K | protein_coding | tolerated(0.12) | benign(0.104) | TCGA-B6-A3ZX-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cyclophosphamide | PD | |
R3HCC1L | SNV | Missense_Mutation | c.2044N>A | p.Ala682Thr | p.A682T | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-BH-A18V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
R3HCC1L | SNV | Missense_Mutation | c.1504N>A | p.Asp502Asn | p.D502N | protein_coding | tolerated(0.17) | benign(0.007) | TCGA-IR-A3LK-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | PD | ||
R3HCC1L | SNV | Missense_Mutation | novel | c.808C>G | p.Pro270Ala | p.P270A | protein_coding | tolerated(0.15) | benign(0.287) | TCGA-VS-AA62-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | PD | |
R3HCC1L | SNV | Missense_Mutation | c.1966N>T | p.His656Tyr | p.H656Y | protein_coding | deleterious(0) | benign(0.017) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | ||
R3HCC1L | SNV | Missense_Mutation | novel | c.258N>T | p.Lys86Asn | p.K86N | protein_coding | deleterious(0) | possibly_damaging(0.885) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
R3HCC1L | SNV | Missense_Mutation | c.1960G>A | p.Glu654Lys | p.E654K | protein_coding | deleterious(0.02) | probably_damaging(0.987) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD | ||
R3HCC1L | SNV | Missense_Mutation | novel | c.744A>C | p.Gln248His | p.Q248H | protein_coding | deleterious(0) | benign(0.067) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
R3HCC1L | SNV | Missense_Mutation | rs373657280 | c.206N>A | p.Arg69Gln | p.R69Q | protein_coding | tolerated(1) | benign(0) | 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 |
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