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Gene: CHIC2 |
Gene summary for CHIC2 |
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Gene information | Species | Human | Gene symbol | CHIC2 | Gene ID | 26511 |
Gene name | cysteine rich hydrophobic domain 2 | |
Gene Alias | BTL | |
Cytomap | 4q12 | |
Gene Type | protein-coding | GO ID | GO:0008150 | UniProtAcc | Q9UKJ5 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
26511 | CHIC2 | AEH-subject1 | Human | Endometrium | AEH | 8.26e-06 | 2.32e-01 | -0.3059 |
26511 | CHIC2 | AEH-subject5 | Human | Endometrium | AEH | 1.91e-02 | 2.06e-01 | -0.2953 |
26511 | CHIC2 | GSM5276934 | Human | Endometrium | EEC | 1.20e-19 | 5.13e-01 | -0.0913 |
26511 | CHIC2 | GSM5276937 | Human | Endometrium | EEC | 1.30e-35 | 7.89e-01 | -0.0897 |
26511 | CHIC2 | GSM6177620_NYU_UCEC1_lib1_lib1 | Human | Endometrium | EEC | 2.32e-04 | -1.58e-01 | -0.1869 |
26511 | CHIC2 | GSM6177620_NYU_UCEC1_lib2_lib2 | Human | Endometrium | EEC | 2.72e-04 | -1.72e-01 | -0.1875 |
26511 | CHIC2 | GSM6177620_NYU_UCEC1_lib3_lib3 | Human | Endometrium | EEC | 9.90e-07 | -1.40e-01 | -0.1883 |
26511 | CHIC2 | GSM6177621_NYU_UCEC2_lib1_lib1 | Human | Endometrium | EEC | 1.43e-07 | -1.46e-01 | -0.1934 |
26511 | CHIC2 | GSM6177622_NYU_UCEC3_lib1_lib1 | Human | Endometrium | EEC | 3.79e-14 | -8.13e-02 | -0.1917 |
26511 | CHIC2 | GSM6177622_NYU_UCEC3_lib2_lib2 | Human | Endometrium | EEC | 1.81e-11 | -1.10e-01 | -0.1916 |
26511 | CHIC2 | LZE2T | Human | Esophagus | ESCC | 2.79e-02 | 3.65e-01 | 0.082 |
26511 | CHIC2 | LZE4T | Human | Esophagus | ESCC | 3.51e-14 | 3.50e-01 | 0.0811 |
26511 | CHIC2 | LZE7T | Human | Esophagus | ESCC | 9.30e-07 | 7.68e-01 | 0.0667 |
26511 | CHIC2 | LZE8T | Human | Esophagus | ESCC | 3.21e-11 | 9.47e-02 | 0.067 |
26511 | CHIC2 | LZE20T | Human | Esophagus | ESCC | 1.60e-11 | 1.57e-01 | 0.0662 |
26511 | CHIC2 | LZE22D1 | Human | Esophagus | HGIN | 1.45e-02 | -7.96e-02 | 0.0595 |
26511 | CHIC2 | LZE24T | Human | Esophagus | ESCC | 1.20e-18 | 5.04e-01 | 0.0596 |
26511 | CHIC2 | LZE6T | Human | Esophagus | ESCC | 9.52e-04 | -3.83e-02 | 0.0845 |
26511 | CHIC2 | P2T-E | Human | Esophagus | ESCC | 1.52e-39 | 7.08e-01 | 0.1177 |
26511 | CHIC2 | P4T-E | Human | Esophagus | ESCC | 1.79e-24 | 5.65e-01 | 0.1323 |
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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 |
CHIC2 | SNV | Missense_Mutation | c.335N>A | p.Arg112Gln | p.R112Q | Q9UKJ5 | protein_coding | tolerated(0.3) | possibly_damaging(0.714) | TCGA-BH-A204-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
CHIC2 | SNV | Missense_Mutation | novel | c.38N>C | p.Asp13Ala | p.D13A | Q9UKJ5 | protein_coding | tolerated(0.23) | probably_damaging(0.968) | TCGA-D8-A1JK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
CHIC2 | SNV | Missense_Mutation | rs750921405 | c.488N>A | p.Arg163Gln | p.R163Q | Q9UKJ5 | protein_coding | tolerated(0.2) | benign(0.019) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
CHIC2 | SNV | Missense_Mutation | c.493N>T | p.Asp165Tyr | p.D165Y | Q9UKJ5 | protein_coding | deleterious(0) | probably_damaging(0.982) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
CHIC2 | SNV | Missense_Mutation | c.464N>A | p.Phe155Tyr | p.F155Y | Q9UKJ5 | protein_coding | tolerated(0.11) | benign(0.015) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR | |
CHIC2 | SNV | Missense_Mutation | novel | c.338G>T | p.Arg113Ile | p.R113I | Q9UKJ5 | protein_coding | tolerated(0.11) | benign(0.029) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
CHIC2 | SNV | Missense_Mutation | c.250C>T | p.Arg84Cys | p.R84C | Q9UKJ5 | protein_coding | deleterious(0) | possibly_damaging(0.873) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
CHIC2 | SNV | Missense_Mutation | rs772144534 | c.131N>A | p.Ser44Asn | p.S44N | Q9UKJ5 | protein_coding | tolerated(0.31) | benign(0.096) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
CHIC2 | SNV | Missense_Mutation | c.146N>A | p.Ser49Tyr | p.S49Y | Q9UKJ5 | protein_coding | deleterious(0.01) | possibly_damaging(0.544) | TCGA-AX-A0J0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
CHIC2 | SNV | Missense_Mutation | novel | c.197C>T | p.Ala66Val | p.A66V | Q9UKJ5 | protein_coding | tolerated(0.14) | benign(0.238) | TCGA-B5-A3FC-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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