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Gene: FAM32A |
Gene summary for FAM32A |
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Gene information | Species | Human | Gene symbol | FAM32A | Gene ID | 26017 |
Gene name | family with sequence similarity 32 member A | |
Gene Alias | OTAG-12 | |
Cytomap | 19p13.11 | |
Gene Type | protein-coding | GO ID | GO:0006915 | UniProtAcc | A0A024R7I4 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
26017 | FAM32A | HTA11_10623_2000001011 | Human | Colorectum | AD | 2.86e-10 | 4.47e-01 | -0.0177 |
26017 | FAM32A | HTA11_6801_2000001011 | Human | Colorectum | SER | 4.53e-03 | 3.76e-01 | 0.0171 |
26017 | FAM32A | HTA11_10711_2000001011 | Human | Colorectum | AD | 2.34e-04 | 2.28e-01 | 0.0338 |
26017 | FAM32A | HTA11_7696_3000711011 | Human | Colorectum | AD | 3.22e-11 | 3.99e-01 | 0.0674 |
26017 | FAM32A | HTA11_6818_2000001021 | Human | Colorectum | AD | 2.11e-04 | 2.72e-01 | 0.0588 |
26017 | FAM32A | HTA11_99999970781_79442 | Human | Colorectum | MSS | 1.82e-13 | 3.68e-01 | 0.294 |
26017 | FAM32A | HTA11_99999965062_69753 | Human | Colorectum | MSI-H | 8.00e-08 | 8.87e-01 | 0.3487 |
26017 | FAM32A | HTA11_99999965104_69814 | Human | Colorectum | MSS | 1.46e-11 | 3.89e-01 | 0.281 |
26017 | FAM32A | HTA11_99999971662_82457 | Human | Colorectum | MSS | 1.23e-19 | 4.72e-01 | 0.3859 |
26017 | FAM32A | HTA11_99999973899_84307 | Human | Colorectum | MSS | 6.29e-15 | 6.10e-01 | 0.2585 |
26017 | FAM32A | HTA11_99999974143_84620 | Human | Colorectum | MSS | 6.14e-09 | 3.04e-01 | 0.3005 |
26017 | FAM32A | LZE2D | Human | Esophagus | HGIN | 1.55e-02 | 9.06e-02 | 0.0642 |
26017 | FAM32A | LZE2T | Human | Esophagus | ESCC | 2.19e-05 | 2.83e-01 | 0.082 |
26017 | FAM32A | LZE3D | Human | Esophagus | HGIN | 2.35e-02 | 2.54e-01 | 0.0668 |
26017 | FAM32A | LZE4T | Human | Esophagus | ESCC | 1.19e-14 | 3.91e-01 | 0.0811 |
26017 | FAM32A | LZE5T | Human | Esophagus | ESCC | 2.22e-02 | 1.84e-01 | 0.0514 |
26017 | FAM32A | LZE7T | Human | Esophagus | ESCC | 2.34e-11 | 8.40e-01 | 0.0667 |
26017 | FAM32A | LZE8T | Human | Esophagus | ESCC | 1.52e-15 | 1.45e-01 | 0.067 |
26017 | FAM32A | LZE20T | Human | Esophagus | ESCC | 3.27e-06 | 1.96e-01 | 0.0662 |
26017 | FAM32A | LZE22D1 | Human | Esophagus | HGIN | 1.55e-06 | 1.12e-01 | 0.0595 |
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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 |
FAM32A | SNV | Missense_Mutation | c.196N>C | p.Glu66Gln | p.E66Q | Q9Y421 | protein_coding | tolerated(0.32) | probably_damaging(0.987) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
FAM32A | SNV | Missense_Mutation | novel | c.271N>A | p.Asp91Asn | p.D91N | Q9Y421 | protein_coding | tolerated(0.09) | benign(0.041) | TCGA-BH-A0B6-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
FAM32A | SNV | Missense_Mutation | c.182N>T | p.Ala61Val | p.A61V | Q9Y421 | protein_coding | deleterious(0.01) | probably_damaging(0.984) | TCGA-A6-6653-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
FAM32A | SNV | Missense_Mutation | novel | c.38A>C | p.Lys13Thr | p.K13T | Q9Y421 | protein_coding | deleterious(0) | probably_damaging(0.961) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
FAM32A | SNV | Missense_Mutation | c.138G>T | p.Lys46Asn | p.K46N | Q9Y421 | protein_coding | tolerated(0.27) | probably_damaging(0.911) | TCGA-BS-A0UV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
FAM32A | SNV | Missense_Mutation | novel | c.121N>G | p.Met41Val | p.M41V | Q9Y421 | protein_coding | tolerated(0.48) | benign(0.028) | TCGA-WX-AA44-01 | Liver | liver hepatocellular carcinoma | Female | <65 | I/II | Targeted Molecular therapy | sorafenib | PR |
FAM32A | SNV | Missense_Mutation | c.332C>T | p.Thr111Met | p.T111M | Q9Y421 | protein_coding | deleterious(0.02) | benign(0.09) | TCGA-44-2657-01 | Lung | lung adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
FAM32A | SNV | Missense_Mutation | novel | c.305N>G | p.His102Arg | p.H102R | Q9Y421 | protein_coding | deleterious(0) | benign(0.029) | TCGA-VQ-A8E3-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | 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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