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Gene: AHDC1 |
Gene summary for AHDC1 |
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Gene information | Species | Human | Gene symbol | AHDC1 | Gene ID | 27245 |
Gene name | AT-hook DNA binding motif containing 1 | |
Gene Alias | MRD25 | |
Cytomap | 1p36.11-p35.3 | |
Gene Type | protein-coding | GO ID | GO:0003674 | UniProtAcc | Q5TGY3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
27245 | AHDC1 | P57T-E | Human | Esophagus | ESCC | 9.45e-14 | 1.89e-01 | 0.0926 |
27245 | AHDC1 | P61T-E | Human | Esophagus | ESCC | 1.65e-02 | 4.31e-02 | 0.099 |
27245 | AHDC1 | P62T-E | Human | Esophagus | ESCC | 4.10e-12 | 2.72e-01 | 0.1302 |
27245 | AHDC1 | P65T-E | Human | Esophagus | ESCC | 7.01e-07 | 1.32e-01 | 0.0978 |
27245 | AHDC1 | P74T-E | Human | Esophagus | ESCC | 2.29e-13 | 4.74e-01 | 0.1479 |
27245 | AHDC1 | P75T-E | Human | Esophagus | ESCC | 2.30e-16 | 3.14e-01 | 0.1125 |
27245 | AHDC1 | P76T-E | Human | Esophagus | ESCC | 9.03e-12 | 1.15e-01 | 0.1207 |
27245 | AHDC1 | P79T-E | Human | Esophagus | ESCC | 1.12e-13 | 1.05e-01 | 0.1154 |
27245 | AHDC1 | P80T-E | Human | Esophagus | ESCC | 3.20e-04 | 1.83e-01 | 0.155 |
27245 | AHDC1 | P82T-E | Human | Esophagus | ESCC | 1.01e-08 | 5.32e-01 | 0.1072 |
27245 | AHDC1 | P83T-E | Human | Esophagus | ESCC | 1.83e-11 | 3.72e-01 | 0.1738 |
27245 | AHDC1 | P84T-E | Human | Esophagus | ESCC | 2.72e-03 | 1.71e-01 | 0.0933 |
27245 | AHDC1 | P89T-E | Human | Esophagus | ESCC | 4.93e-02 | 1.55e-01 | 0.1752 |
27245 | AHDC1 | P91T-E | Human | Esophagus | ESCC | 7.30e-05 | 5.01e-01 | 0.1828 |
27245 | AHDC1 | P107T-E | Human | Esophagus | ESCC | 1.97e-13 | 3.41e-01 | 0.171 |
27245 | AHDC1 | P126T-E | Human | Esophagus | ESCC | 2.02e-02 | 6.11e-01 | 0.1125 |
27245 | AHDC1 | P127T-E | Human | Esophagus | ESCC | 6.85e-07 | 6.76e-02 | 0.0826 |
27245 | AHDC1 | P128T-E | Human | Esophagus | ESCC | 1.15e-21 | 9.13e-01 | 0.1241 |
27245 | AHDC1 | P130T-E | Human | Esophagus | ESCC | 1.79e-17 | 3.18e-01 | 0.1676 |
27245 | AHDC1 | HCC1_Meng | Human | Liver | HCC | 1.78e-09 | -4.31e-02 | 0.0246 |
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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 |
AHDC1 | SNV | Missense_Mutation | c.607G>C | p.Glu203Gln | p.E203Q | Q5TGY3 | protein_coding | tolerated_low_confidence(0.42) | possibly_damaging(0.859) | TCGA-C8-A26Y-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
AHDC1 | insertion | Frame_Shift_Ins | novel | c.4176dupC | p.Gly1393ArgfsTer88 | p.G1393Rfs*88 | Q5TGY3 | protein_coding | TCGA-BH-A0BZ-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | CR | ||
AHDC1 | SNV | Missense_Mutation | rs377405108 | c.3857G>A | p.Arg1286Gln | p.R1286Q | Q5TGY3 | protein_coding | tolerated(0.08) | possibly_damaging(0.728) | TCGA-MU-A5YI-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | PD |
AHDC1 | SNV | Missense_Mutation | rs757919190 | c.460N>T | p.Arg154Cys | p.R154C | Q5TGY3 | protein_coding | tolerated_low_confidence(0.06) | possibly_damaging(0.542) | TCGA-A6-2672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
AHDC1 | SNV | Missense_Mutation | c.3703C>T | p.Arg1235Trp | p.R1235W | Q5TGY3 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AA-3710-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
AHDC1 | SNV | Missense_Mutation | rs766744511 | c.3256N>G | p.Ser1086Ala | p.S1086A | Q5TGY3 | protein_coding | tolerated_low_confidence(0.9) | possibly_damaging(0.525) | TCGA-AA-3713-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | 5-fluorouracil | PR |
AHDC1 | SNV | Missense_Mutation | rs754239206 | c.2594G>A | p.Arg865Gln | p.R865Q | Q5TGY3 | protein_coding | deleterious(0.01) | benign(0.236) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
AHDC1 | SNV | Missense_Mutation | rs766744511 | c.3256N>G | p.Ser1086Ala | p.S1086A | Q5TGY3 | protein_coding | tolerated_low_confidence(0.9) | possibly_damaging(0.525) | TCGA-AA-3966-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
AHDC1 | SNV | Missense_Mutation | rs764325293 | c.668N>T | p.Thr223Met | p.T223M | Q5TGY3 | protein_coding | deleterious_low_confidence(0.03) | possibly_damaging(0.706) | TCGA-AD-6895-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD |
AHDC1 | SNV | Missense_Mutation | c.3415C>T | p.Pro1139Ser | p.P1139S | Q5TGY3 | protein_coding | tolerated(0.33) | benign(0.147) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD |
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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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