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Gene: UBAC1 |
Gene summary for UBAC1 |
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Gene information | Species | Human | Gene symbol | UBAC1 | Gene ID | 10422 |
Gene name | UBA domain containing 1 | |
Gene Alias | GBDR1 | |
Cytomap | 9q34.3 | |
Gene Type | protein-coding | GO ID | GO:0006464 | UniProtAcc | A0A140VK64 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
10422 | UBAC1 | HTA11_347_2000001011 | Human | Colorectum | AD | 2.90e-04 | 2.90e-01 | -0.1954 |
10422 | UBAC1 | HTA11_83_2000001011 | Human | Colorectum | SER | 7.48e-05 | 3.75e-01 | -0.1526 |
10422 | UBAC1 | HTA11_7469_2000001011 | Human | Colorectum | AD | 1.32e-02 | 5.05e-01 | -0.0124 |
10422 | UBAC1 | A014-C-008 | Human | Colorectum | FAP | 3.72e-02 | -2.00e-01 | -0.191 |
10422 | UBAC1 | LZE2T | Human | Esophagus | ESCC | 3.66e-07 | 7.36e-01 | 0.082 |
10422 | UBAC1 | LZE4T | Human | Esophagus | ESCC | 1.36e-05 | 2.08e-01 | 0.0811 |
10422 | UBAC1 | LZE7T | Human | Esophagus | ESCC | 7.43e-03 | 2.53e-01 | 0.0667 |
10422 | UBAC1 | LZE8T | Human | Esophagus | ESCC | 6.14e-05 | 2.36e-01 | 0.067 |
10422 | UBAC1 | LZE20T | Human | Esophagus | ESCC | 1.71e-12 | 5.04e-01 | 0.0662 |
10422 | UBAC1 | LZE22T | Human | Esophagus | ESCC | 2.53e-02 | 3.84e-01 | 0.068 |
10422 | UBAC1 | LZE24T | Human | Esophagus | ESCC | 6.84e-06 | 2.42e-01 | 0.0596 |
10422 | UBAC1 | LZE21T | Human | Esophagus | ESCC | 2.47e-05 | 4.66e-01 | 0.0655 |
10422 | UBAC1 | LZE6T | Human | Esophagus | ESCC | 2.17e-03 | 3.56e-01 | 0.0845 |
10422 | UBAC1 | P1T-E | Human | Esophagus | ESCC | 1.83e-17 | 6.69e-01 | 0.0875 |
10422 | UBAC1 | P2T-E | Human | Esophagus | ESCC | 2.37e-27 | 5.09e-01 | 0.1177 |
10422 | UBAC1 | P4T-E | Human | Esophagus | ESCC | 7.28e-22 | 5.43e-01 | 0.1323 |
10422 | UBAC1 | P5T-E | Human | Esophagus | ESCC | 3.56e-27 | 4.95e-01 | 0.1327 |
10422 | UBAC1 | P8T-E | Human | Esophagus | ESCC | 2.49e-32 | 7.25e-01 | 0.0889 |
10422 | UBAC1 | P9T-E | Human | Esophagus | ESCC | 2.13e-20 | 5.01e-01 | 0.1131 |
10422 | UBAC1 | P10T-E | Human | Esophagus | ESCC | 4.22e-17 | 1.74e-01 | 0.116 |
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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 |
Esophagus | ESCC | ![]() |
Skin | AK | ![]() |
Skin | SCCIS | ![]() |
Skin | cSCC | ![]() |
Thyroid | HT | ![]() |
∗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 |
UBAC1 | insertion | Frame_Shift_Ins | novel | c.779_780insGTGTGGCACTGATCGTTTCCTTGGGGTGTGTG | p.Ala261CysfsTer25 | p.A261Cfs*25 | Q9BSL1 | protein_coding | TCGA-A8-A08H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
UBAC1 | SNV | Missense_Mutation | novel | c.325N>C | p.Glu109Gln | p.E109Q | Q9BSL1 | protein_coding | deleterious(0.04) | benign(0.107) | TCGA-VS-A8EL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
UBAC1 | SNV | Missense_Mutation | c.877N>A | p.Ala293Thr | p.A293T | Q9BSL1 | protein_coding | deleterious(0) | probably_damaging(0.979) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
UBAC1 | SNV | Missense_Mutation | novel | c.385N>A | p.Ala129Thr | p.A129T | Q9BSL1 | protein_coding | tolerated(0.06) | benign(0.161) | TCGA-AA-3949-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
UBAC1 | SNV | Missense_Mutation | novel | c.791N>A | p.Ser264Asn | p.S264N | Q9BSL1 | protein_coding | tolerated(0.15) | benign(0) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD |
UBAC1 | SNV | Missense_Mutation | c.1154N>T | p.Asp385Val | p.D385V | Q9BSL1 | protein_coding | deleterious(0) | probably_damaging(0.992) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
UBAC1 | SNV | Missense_Mutation | rs559087791 | c.284G>A | p.Arg95His | p.R95H | Q9BSL1 | protein_coding | deleterious(0) | possibly_damaging(0.869) | TCGA-G4-6588-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
UBAC1 | SNV | Missense_Mutation | novel | c.492N>T | p.Gln164His | p.Q164H | Q9BSL1 | protein_coding | tolerated(0.07) | benign(0.035) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
UBAC1 | SNV | Missense_Mutation | novel | c.910N>A | p.Glu304Lys | p.E304K | Q9BSL1 | protein_coding | deleterious(0) | probably_damaging(0.94) | TCGA-AJ-A3EL-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
UBAC1 | SNV | Missense_Mutation | c.1044N>T | p.Gln348His | p.Q348H | Q9BSL1 | protein_coding | deleterious(0.01) | possibly_damaging(0.85) | TCGA-AP-A059-01 | 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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