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Gene: ZC2HC1A |
Gene summary for ZC2HC1A |
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Gene information | Species | Human | Gene symbol | ZC2HC1A | Gene ID | 51101 |
Gene name | zinc finger C2HC-type containing 1A | |
Gene Alias | C8orf70 | |
Cytomap | 8q21.13 | |
Gene Type | protein-coding | GO ID | GO:0003674 | UniProtAcc | B2R9B8 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
51101 | ZC2HC1A | LZE4T | Human | Esophagus | ESCC | 1.43e-10 | 3.61e-01 | 0.0811 |
51101 | ZC2HC1A | LZE8T | Human | Esophagus | ESCC | 2.94e-09 | 2.56e-01 | 0.067 |
51101 | ZC2HC1A | LZE24T | Human | Esophagus | ESCC | 8.22e-13 | 4.30e-01 | 0.0596 |
51101 | ZC2HC1A | P1T-E | Human | Esophagus | ESCC | 1.09e-04 | 4.24e-01 | 0.0875 |
51101 | ZC2HC1A | P2T-E | Human | Esophagus | ESCC | 3.10e-22 | 3.65e-01 | 0.1177 |
51101 | ZC2HC1A | P4T-E | Human | Esophagus | ESCC | 2.12e-18 | 4.63e-01 | 0.1323 |
51101 | ZC2HC1A | P5T-E | Human | Esophagus | ESCC | 3.58e-06 | 1.10e-01 | 0.1327 |
51101 | ZC2HC1A | P8T-E | Human | Esophagus | ESCC | 1.94e-24 | 4.21e-01 | 0.0889 |
51101 | ZC2HC1A | P9T-E | Human | Esophagus | ESCC | 1.32e-04 | 1.50e-01 | 0.1131 |
51101 | ZC2HC1A | P10T-E | Human | Esophagus | ESCC | 2.39e-23 | 2.96e-01 | 0.116 |
51101 | ZC2HC1A | P11T-E | Human | Esophagus | ESCC | 1.13e-14 | 5.02e-01 | 0.1426 |
51101 | ZC2HC1A | P12T-E | Human | Esophagus | ESCC | 5.23e-03 | 1.23e-02 | 0.1122 |
51101 | ZC2HC1A | P15T-E | Human | Esophagus | ESCC | 4.65e-05 | 1.76e-01 | 0.1149 |
51101 | ZC2HC1A | P16T-E | Human | Esophagus | ESCC | 4.85e-55 | 1.03e+00 | 0.1153 |
51101 | ZC2HC1A | P17T-E | Human | Esophagus | ESCC | 3.54e-09 | 2.73e-01 | 0.1278 |
51101 | ZC2HC1A | P20T-E | Human | Esophagus | ESCC | 6.08e-10 | 6.88e-02 | 0.1124 |
51101 | ZC2HC1A | P21T-E | Human | Esophagus | ESCC | 1.35e-03 | 1.15e-02 | 0.1617 |
51101 | ZC2HC1A | P22T-E | Human | Esophagus | ESCC | 2.97e-19 | 3.46e-01 | 0.1236 |
51101 | ZC2HC1A | P23T-E | Human | Esophagus | ESCC | 2.84e-02 | 1.85e-01 | 0.108 |
51101 | ZC2HC1A | P24T-E | Human | Esophagus | ESCC | 5.40e-12 | 1.20e-01 | 0.1287 |
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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 |
ZC2HC1A | SNV | Missense_Mutation | c.162G>T | p.Gln54His | p.Q54H | Q96GY0 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-BR-4257-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
ZC2HC1A | SNV | Missense_Mutation | c.941N>C | p.Phe314Ser | p.F314S | Q96GY0 | protein_coding | deleterious(0) | possibly_damaging(0.572) | TCGA-BR-8680-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | oxaliplatin | CR | |
ZC2HC1A | SNV | Missense_Mutation | c.569N>C | p.Leu190Ser | p.L190S | Q96GY0 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-HU-8602-01 | Stomach | stomach adenocarcinoma | Female | <65 | I/II | Chemotherapy | xeloda | CR | |
ZC2HC1A | SNV | Missense_Mutation | novel | c.844N>A | p.Gly282Ser | p.G282S | Q96GY0 | protein_coding | tolerated(0.24) | benign(0.251) | TCGA-VQ-A8P2-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Unspecific | Complete Response | |
ZC2HC1A | SNV | Missense_Mutation | c.162N>C | p.Gln54His | p.Q54H | Q96GY0 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-VQ-AA6K-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | fluorouracil | PD | |
ZC2HC1A | deletion | Frame_Shift_Del | novel | c.130delN | p.Lys45AsnfsTer20 | p.K45Nfs*20 | Q96GY0 | protein_coding | TCGA-BR-8372-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | etoposide | CR | ||
ZC2HC1A | deletion | Frame_Shift_Del | novel | c.99delA | p.Lys33AsnfsTer32 | p.K33Nfs*32 | Q96GY0 | protein_coding | TCGA-HU-A4G8-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Chemotherapy | 5-fluorouracil | SD | ||
ZC2HC1A | insertion | Nonsense_Mutation | novel | c.160_161insCAGTTTAAAAATCTG | p.Gln54delinsProValTerLysSerGlu | p.Q54delinsPV*KSE | Q96GY0 | protein_coding | TCGA-FY-A4B0-01 | Thyroid | thyroid carcinoma | Male | >=65 | I/II | Hormone Therapy | synthroid | 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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