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Gene: ABRACL |
Gene summary for ABRACL |
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Gene information | Species | Human | Gene symbol | ABRACL | Gene ID | 58527 |
Gene name | ABRA C-terminal like | |
Gene Alias | C6orf115 | |
Cytomap | 6q24.1 | |
Gene Type | protein-coding | GO ID | GO:0008150 | UniProtAcc | Q9P1F3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
58527 | ABRACL | P57T-E | Human | Esophagus | ESCC | 1.92e-12 | 3.58e-01 | 0.0926 |
58527 | ABRACL | P61T-E | Human | Esophagus | ESCC | 3.19e-15 | 7.21e-01 | 0.099 |
58527 | ABRACL | P62T-E | Human | Esophagus | ESCC | 4.66e-72 | 1.47e+00 | 0.1302 |
58527 | ABRACL | P65T-E | Human | Esophagus | ESCC | 4.24e-34 | 8.62e-01 | 0.0978 |
58527 | ABRACL | P74T-E | Human | Esophagus | ESCC | 9.27e-43 | 1.42e+00 | 0.1479 |
58527 | ABRACL | P75T-E | Human | Esophagus | ESCC | 5.03e-66 | 1.50e+00 | 0.1125 |
58527 | ABRACL | P76T-E | Human | Esophagus | ESCC | 7.69e-29 | 8.10e-01 | 0.1207 |
58527 | ABRACL | P79T-E | Human | Esophagus | ESCC | 7.17e-67 | 1.64e+00 | 0.1154 |
58527 | ABRACL | P80T-E | Human | Esophagus | ESCC | 2.40e-51 | 1.75e+00 | 0.155 |
58527 | ABRACL | P82T-E | Human | Esophagus | ESCC | 5.08e-20 | 1.71e+00 | 0.1072 |
58527 | ABRACL | P83T-E | Human | Esophagus | ESCC | 2.14e-41 | 1.41e+00 | 0.1738 |
58527 | ABRACL | P84T-E | Human | Esophagus | ESCC | 4.22e-11 | 1.07e+00 | 0.0933 |
58527 | ABRACL | P89T-E | Human | Esophagus | ESCC | 9.31e-30 | 2.31e+00 | 0.1752 |
58527 | ABRACL | P91T-E | Human | Esophagus | ESCC | 2.57e-17 | 1.78e+00 | 0.1828 |
58527 | ABRACL | P94T-E | Human | Esophagus | ESCC | 3.84e-02 | 1.04e+00 | 0.0879 |
58527 | ABRACL | P107T-E | Human | Esophagus | ESCC | 1.57e-49 | 1.42e+00 | 0.171 |
58527 | ABRACL | P126T-E | Human | Esophagus | ESCC | 1.92e-09 | 1.09e+00 | 0.1125 |
58527 | ABRACL | P127T-E | Human | Esophagus | ESCC | 9.69e-17 | 5.12e-01 | 0.0826 |
58527 | ABRACL | P128T-E | Human | Esophagus | ESCC | 6.56e-62 | 2.48e+00 | 0.1241 |
58527 | ABRACL | P130T-E | Human | Esophagus | ESCC | 8.05e-80 | 2.69e+00 | 0.1676 |
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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 |
GO:00329709 | Breast | Precancer | regulation of actin filament-based process | 42/1080 | 397/18723 | 1.11e-04 | 2.01e-03 | 42 |
GO:003297014 | Breast | IDC | regulation of actin filament-based process | 56/1434 | 397/18723 | 6.37e-06 | 1.99e-04 | 56 |
GO:003297024 | Breast | DCIS | regulation of actin filament-based process | 56/1390 | 397/18723 | 2.50e-06 | 8.74e-05 | 56 |
GO:0032970 | Colorectum | AD | regulation of actin filament-based process | 142/3918 | 397/18723 | 4.05e-12 | 5.90e-10 | 142 |
GO:00329702 | Colorectum | MSS | regulation of actin filament-based process | 128/3467 | 397/18723 | 2.47e-11 | 3.49e-09 | 128 |
GO:00329704 | Colorectum | FAP | regulation of actin filament-based process | 105/2622 | 397/18723 | 3.15e-11 | 1.38e-08 | 105 |
GO:003297027 | Esophagus | HGIN | regulation of actin filament-based process | 77/2587 | 397/18723 | 1.14e-03 | 1.39e-02 | 77 |
GO:0032970111 | Esophagus | ESCC | regulation of actin filament-based process | 231/8552 | 397/18723 | 2.91e-07 | 4.20e-06 | 231 |
GO:003297012 | Liver | Cirrhotic | regulation of actin filament-based process | 152/4634 | 397/18723 | 1.12e-09 | 5.00e-08 | 152 |
GO:003297022 | Liver | HCC | regulation of actin filament-based process | 222/7958 | 397/18723 | 3.81e-08 | 8.30e-07 | 222 |
GO:003297020 | Oral cavity | OSCC | regulation of actin filament-based process | 209/7305 | 397/18723 | 1.89e-08 | 3.72e-07 | 209 |
GO:0032970110 | Oral cavity | LP | regulation of actin filament-based process | 133/4623 | 397/18723 | 4.21e-05 | 6.09e-04 | 133 |
GO:003297018 | Prostate | BPH | regulation of actin filament-based process | 133/3107 | 397/18723 | 7.07e-17 | 1.62e-14 | 133 |
GO:003297019 | Prostate | Tumor | regulation of actin filament-based process | 133/3246 | 397/18723 | 2.59e-15 | 4.35e-13 | 133 |
GO:003297029 | Skin | cSCC | regulation of actin filament-based process | 142/4864 | 397/18723 | 8.50e-06 | 1.13e-04 | 142 |
GO:0032970113 | Thyroid | PTC | regulation of actin filament-based process | 197/5968 | 397/18723 | 8.91e-14 | 4.89e-12 | 197 |
GO:0032970210 | Thyroid | ATC | regulation of actin filament-based process | 208/6293 | 397/18723 | 5.82e-15 | 3.80e-13 | 208 |
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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 |
ABRACL | SNV | Missense_Mutation | novel | c.37G>A | p.Glu13Lys | p.E13K | Q9P1F3 | protein_coding | tolerated(0.41) | benign(0.242) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
ABRACL | SNV | Missense_Mutation | rs772960368 | c.164N>A | p.Arg55Gln | p.R55Q | Q9P1F3 | protein_coding | tolerated(0.07) | benign(0.044) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ABRACL | SNV | Missense_Mutation | novel | c.132N>C | p.Glu44Asp | p.E44D | Q9P1F3 | protein_coding | deleterious(0.04) | probably_damaging(0.996) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
ABRACL | SNV | Missense_Mutation | c.31G>C | p.Val11Leu | p.V11L | Q9P1F3 | protein_coding | tolerated(0.4) | benign(0.059) | TCGA-44-3918-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | SD | |
ABRACL | SNV | Missense_Mutation | novel | c.154N>T | p.Ala52Ser | p.A52S | Q9P1F3 | protein_coding | tolerated(0.07) | benign(0.103) | TCGA-VQ-A91S-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | fluorouracil | CR |
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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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