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Gene: ANKRD13A |
Gene summary for ANKRD13A |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | ANKRD13A | Gene ID | 88455 |
| Gene name | ankyrin repeat domain 13A | |
| Gene Alias | ANKRD13 | |
| Cytomap | 12q24.11 | |
| Gene Type | protein-coding | GO ID | GO:0002090 | UniProtAcc | Q3ZTS7 |
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Malignant transformation analysis |
| Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
| Malignant transformation involving gene list. |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 88455 | ANKRD13A | P32T-E | Human | Esophagus | ESCC | 2.59e-03 | 9.55e-03 | 0.1666 |
| 88455 | ANKRD13A | P36T-E | Human | Esophagus | ESCC | 8.41e-07 | 2.60e-01 | 0.1187 |
| 88455 | ANKRD13A | P37T-E | Human | Esophagus | ESCC | 4.02e-03 | 1.26e-01 | 0.1371 |
| 88455 | ANKRD13A | P39T-E | Human | Esophagus | ESCC | 1.78e-05 | 1.50e-01 | 0.0894 |
| 88455 | ANKRD13A | P40T-E | Human | Esophagus | ESCC | 1.66e-04 | 1.64e-01 | 0.109 |
| 88455 | ANKRD13A | P44T-E | Human | Esophagus | ESCC | 1.33e-05 | 1.38e-01 | 0.1096 |
| 88455 | ANKRD13A | P47T-E | Human | Esophagus | ESCC | 4.21e-05 | 8.56e-02 | 0.1067 |
| 88455 | ANKRD13A | P48T-E | Human | Esophagus | ESCC | 4.62e-03 | 5.74e-02 | 0.0959 |
| 88455 | ANKRD13A | P52T-E | Human | Esophagus | ESCC | 3.54e-05 | 6.49e-02 | 0.1555 |
| 88455 | ANKRD13A | P54T-E | Human | Esophagus | ESCC | 4.54e-07 | 1.90e-01 | 0.0975 |
| 88455 | ANKRD13A | P57T-E | Human | Esophagus | ESCC | 1.13e-05 | 1.15e-01 | 0.0926 |
| 88455 | ANKRD13A | P61T-E | Human | Esophagus | ESCC | 6.19e-06 | 1.77e-01 | 0.099 |
| 88455 | ANKRD13A | P62T-E | Human | Esophagus | ESCC | 2.60e-15 | 3.05e-01 | 0.1302 |
| 88455 | ANKRD13A | P65T-E | Human | Esophagus | ESCC | 6.78e-06 | 1.16e-01 | 0.0978 |
| 88455 | ANKRD13A | P74T-E | Human | Esophagus | ESCC | 1.77e-02 | 1.70e-01 | 0.1479 |
| 88455 | ANKRD13A | P75T-E | Human | Esophagus | ESCC | 2.23e-13 | 1.79e-01 | 0.1125 |
| 88455 | ANKRD13A | P76T-E | Human | Esophagus | ESCC | 6.10e-04 | 1.05e-02 | 0.1207 |
| 88455 | ANKRD13A | P80T-E | Human | Esophagus | ESCC | 8.42e-11 | 3.03e-01 | 0.155 |
| 88455 | ANKRD13A | P82T-E | Human | Esophagus | ESCC | 2.10e-04 | 7.33e-01 | 0.1072 |
| 88455 | ANKRD13A | P107T-E | Human | Esophagus | ESCC | 6.67e-03 | 7.43e-02 | 0.171 |
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| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia | ||
| NEOLP: Non-erosive oral lichen planus | ||
| OSCC: Oral squamous cell carcinoma |
| ∗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 |
| Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
| Figure of enriched GO biological processes. |
| 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 |
| Enriched GO biological processes. |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| GO:003010018 | Esophagus | ESCC | regulation of endocytosis | 135/8552 | 211/18723 | 5.75e-08 | 1.02e-06 | 135 |
| GO:004311218 | Esophagus | ESCC | receptor metabolic process | 104/8552 | 166/18723 | 7.44e-06 | 7.37e-05 | 104 |
| GO:19038289 | Esophagus | ESCC | negative regulation of cellular protein localization | 76/8552 | 117/18723 | 1.97e-05 | 1.72e-04 | 76 |
| GO:000689818 | Esophagus | ESCC | receptor-mediated endocytosis | 142/8552 | 244/18723 | 5.22e-05 | 4.05e-04 | 142 |
| GO:004825916 | Esophagus | ESCC | regulation of receptor-mediated endocytosis | 66/8552 | 110/18723 | 1.72e-03 | 7.96e-03 | 66 |
| GO:00360106 | Esophagus | ESCC | protein localization to endosome | 18/8552 | 24/18723 | 3.43e-03 | 1.41e-02 | 18 |
| GO:003010016 | Oral cavity | OSCC | regulation of endocytosis | 121/7305 | 211/18723 | 4.74e-08 | 8.80e-07 | 121 |
| GO:000689810 | Oral cavity | OSCC | receptor-mediated endocytosis | 125/7305 | 244/18723 | 6.56e-05 | 5.32e-04 | 125 |
| GO:004311210 | Oral cavity | OSCC | receptor metabolic process | 88/7305 | 166/18723 | 1.68e-04 | 1.15e-03 | 88 |
| GO:19038288 | Oral cavity | OSCC | negative regulation of cellular protein localization | 65/7305 | 117/18723 | 2.05e-04 | 1.36e-03 | 65 |
| GO:004825910 | Oral cavity | OSCC | regulation of receptor-mediated endocytosis | 58/7305 | 110/18723 | 2.37e-03 | 1.05e-02 | 58 |
| GO:00360105 | Oral cavity | OSCC | protein localization to endosome | 16/7305 | 24/18723 | 5.63e-03 | 2.17e-02 | 16 |
| GO:00316239 | Oral cavity | OSCC | receptor internalization | 56/7305 | 113/18723 | 1.44e-02 | 4.69e-02 | 56 |
| GO:003010017 | Oral cavity | LP | regulation of endocytosis | 81/4623 | 211/18723 | 6.57e-06 | 1.29e-04 | 81 |
| GO:190382813 | Oral cavity | LP | negative regulation of cellular protein localization | 49/4623 | 117/18723 | 3.18e-05 | 4.89e-04 | 49 |
| GO:004311216 | Oral cavity | LP | receptor metabolic process | 64/4623 | 166/18723 | 5.00e-05 | 7.02e-04 | 64 |
| GO:000689817 | Oral cavity | LP | receptor-mediated endocytosis | 87/4623 | 244/18723 | 7.83e-05 | 1.02e-03 | 87 |
| GO:003601012 | Oral cavity | LP | protein localization to endosome | 14/4623 | 24/18723 | 4.52e-04 | 4.30e-03 | 14 |
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| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
| Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
| Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
| Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
| 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 |
| Annotation of somatic variants for genes involved in malignant transformation |
| 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 |
| ANKRD13A | SNV | Missense_Mutation | c.524G>T | p.Ser175Ile | p.S175I | Q8IZ07 | protein_coding | deleterious(0) | possibly_damaging(0.875) | TCGA-B6-A1KC-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| ANKRD13A | SNV | Missense_Mutation | novel | c.967N>T | p.Thr323Ser | p.T323S | Q8IZ07 | protein_coding | tolerated(1) | benign(0.41) | TCGA-D8-A73U-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | SD |
| ANKRD13A | insertion | Nonsense_Mutation | novel | c.1198_1199insGTGTGGAGTAAAGCTGCTGTTGTCTAGCCTACTGCAT | p.Lys400SerfsTer4 | p.K400Sfs*4 | Q8IZ07 | protein_coding | TCGA-A8-A0AD-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
| ANKRD13A | insertion | Frame_Shift_Ins | novel | c.523_524insCTACT | p.Ser175ThrfsTer15 | p.S175Tfs*15 | Q8IZ07 | protein_coding | TCGA-AC-A3QQ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
| ANKRD13A | insertion | Frame_Shift_Ins | novel | c.1054_1055insGGTTAACACGTCCACCTCAGACACTGAGTGCC | p.Glu352GlyfsTer13 | p.E352Gfs*13 | Q8IZ07 | protein_coding | TCGA-BH-A0DS-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | cyclophosphamide | SD | ||
| ANKRD13A | SNV | Missense_Mutation | novel | c.437N>A | p.Cys146Tyr | p.C146Y | Q8IZ07 | protein_coding | tolerated(1) | probably_damaging(0.996) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| ANKRD13A | SNV | Missense_Mutation | novel | c.631N>T | p.Leu211Phe | p.L211F | Q8IZ07 | protein_coding | tolerated(0.24) | possibly_damaging(0.757) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| ANKRD13A | SNV | Missense_Mutation | novel | c.886N>C | p.Asp296His | p.D296H | Q8IZ07 | protein_coding | tolerated(0.06) | probably_damaging(0.979) | TCGA-C5-A1BQ-01 | Cervix | cervical & endocervical cancer | Female | >=65 | III/IV | Chemotherapy | cisplatin | CR |
| ANKRD13A | SNV | Missense_Mutation | rs769790065 | c.214N>T | p.Arg72Cys | p.R72C | Q8IZ07 | protein_coding | tolerated(0.19) | benign(0.001) | TCGA-A6-2686-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| ANKRD13A | SNV | Missense_Mutation | c.629N>A | p.Arg210His | p.R210H | Q8IZ07 | protein_coding | tolerated(0.09) | benign(0.019) | TCGA-AA-3715-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
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Related drugs of malignant transformation related genes |
| Identification of chemicals and drugs interact with genes involved in malignant transfromation |
| (DGIdb 4.0) |
| Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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