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Gene: RCAN3 |
Gene summary for RCAN3 |
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Gene information | Species | Human | Gene symbol | RCAN3 | Gene ID | 11123 |
Gene name | RCAN family member 3 | |
Gene Alias | DSCR1L2 | |
Cytomap | 1p36.11 | |
Gene Type | protein-coding | GO ID | GO:0007154 | UniProtAcc | A0A024RAH2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
11123 | RCAN3 | LZE2T | Human | Esophagus | ESCC | 4.08e-05 | 4.78e-01 | 0.082 |
11123 | RCAN3 | LZE4T | Human | Esophagus | ESCC | 9.07e-09 | 1.66e-01 | 0.0811 |
11123 | RCAN3 | LZE7T | Human | Esophagus | ESCC | 8.02e-06 | 2.64e-01 | 0.0667 |
11123 | RCAN3 | LZE20T | Human | Esophagus | ESCC | 1.11e-04 | 1.50e-01 | 0.0662 |
11123 | RCAN3 | LZE22T | Human | Esophagus | ESCC | 2.30e-04 | 4.04e-01 | 0.068 |
11123 | RCAN3 | LZE24T | Human | Esophagus | ESCC | 4.64e-15 | 3.55e-01 | 0.0596 |
11123 | RCAN3 | P1T-E | Human | Esophagus | ESCC | 1.09e-04 | 2.59e-01 | 0.0875 |
11123 | RCAN3 | P2T-E | Human | Esophagus | ESCC | 9.21e-10 | 2.21e-01 | 0.1177 |
11123 | RCAN3 | P4T-E | Human | Esophagus | ESCC | 3.48e-09 | 2.73e-01 | 0.1323 |
11123 | RCAN3 | P5T-E | Human | Esophagus | ESCC | 4.21e-08 | 1.67e-01 | 0.1327 |
11123 | RCAN3 | P8T-E | Human | Esophagus | ESCC | 6.91e-09 | 2.06e-01 | 0.0889 |
11123 | RCAN3 | P9T-E | Human | Esophagus | ESCC | 4.81e-05 | 1.59e-01 | 0.1131 |
11123 | RCAN3 | P10T-E | Human | Esophagus | ESCC | 2.64e-37 | 7.22e-01 | 0.116 |
11123 | RCAN3 | P11T-E | Human | Esophagus | ESCC | 2.82e-08 | 3.53e-01 | 0.1426 |
11123 | RCAN3 | P12T-E | Human | Esophagus | ESCC | 5.48e-26 | 5.10e-01 | 0.1122 |
11123 | RCAN3 | P15T-E | Human | Esophagus | ESCC | 6.27e-22 | 5.84e-01 | 0.1149 |
11123 | RCAN3 | P16T-E | Human | Esophagus | ESCC | 1.54e-11 | 1.70e-01 | 0.1153 |
11123 | RCAN3 | P17T-E | Human | Esophagus | ESCC | 6.14e-06 | 2.78e-01 | 0.1278 |
11123 | RCAN3 | P19T-E | Human | Esophagus | ESCC | 1.19e-05 | 6.12e-01 | 0.1662 |
11123 | RCAN3 | P20T-E | Human | Esophagus | ESCC | 8.00e-23 | 5.48e-01 | 0.1124 |
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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 |
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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 |
RCAN3 | SNV | Missense_Mutation | c.349N>G | p.Leu117Val | p.L117V | Q9UKA8 | protein_coding | tolerated(0.05) | probably_damaging(0.999) | TCGA-C5-A1MH-01 | Cervix | cervical & endocervical cancer | Female | >=65 | III/IV | Chemotherapy | cisplatin | PD | |
RCAN3 | SNV | Missense_Mutation | c.610N>A | p.Glu204Lys | p.E204K | Q9UKA8 | protein_coding | tolerated(0.07) | probably_damaging(0.997) | TCGA-DR-A0ZM-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Unspecific | Cisplatin | SD | |
RCAN3 | SNV | Missense_Mutation | rs777266872 | c.325G>A | p.Glu109Lys | p.E109K | Q9UKA8 | protein_coding | tolerated(0.4) | possibly_damaging(0.479) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
RCAN3 | SNV | Missense_Mutation | novel | c.71A>G | p.Glu24Gly | p.E24G | Q9UKA8 | protein_coding | deleterious(0.03) | probably_damaging(0.986) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
RCAN3 | SNV | Missense_Mutation | novel | c.671N>T | p.Pro224Leu | p.P224L | Q9UKA8 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AP-A1DK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
RCAN3 | SNV | Missense_Mutation | novel | c.23N>T | p.Ser8Phe | p.S8F | Q9UKA8 | protein_coding | deleterious_low_confidence(0) | possibly_damaging(0.603) | TCGA-AP-A1DV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
RCAN3 | SNV | Missense_Mutation | rs553942744 | c.718N>A | p.Ala240Thr | p.A240T | Q9UKA8 | protein_coding | tolerated_low_confidence(0.53) | benign(0) | TCGA-AX-A0J1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
RCAN3 | SNV | Missense_Mutation | novel | c.211C>A | p.Leu71Ile | p.L71I | Q9UKA8 | protein_coding | deleterious(0.04) | possibly_damaging(0.817) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
RCAN3 | SNV | Missense_Mutation | novel | c.470G>T | p.Trp157Leu | p.W157L | Q9UKA8 | protein_coding | deleterious(0.03) | benign(0.033) | TCGA-B5-A1MX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Hormone Therapy | megace | SD |
RCAN3 | SNV | Missense_Mutation | rs764690503 | c.488N>T | p.Ala163Val | p.A163V | Q9UKA8 | protein_coding | deleterious(0) | possibly_damaging(0.753) | TCGA-D1-A15X-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | 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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