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Gene: FAM104A |
Gene summary for FAM104A |
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Gene information | Species | Human | Gene symbol | FAM104A | Gene ID | 84923 |
Gene name | family with sequence similarity 104 member A | |
Gene Alias | FAM104A | |
Cytomap | 17q25.1 | |
Gene Type | protein-coding | GO ID | GO:0003674 | UniProtAcc | Q969W3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
84923 | FAM104A | LZE2T | Human | Esophagus | ESCC | 8.71e-03 | 3.93e-01 | 0.082 |
84923 | FAM104A | LZE4T | Human | Esophagus | ESCC | 3.31e-14 | 3.93e-01 | 0.0811 |
84923 | FAM104A | LZE5T | Human | Esophagus | ESCC | 9.94e-03 | 2.35e-01 | 0.0514 |
84923 | FAM104A | LZE7T | Human | Esophagus | ESCC | 2.79e-05 | 4.48e-01 | 0.0667 |
84923 | FAM104A | LZE8T | Human | Esophagus | ESCC | 1.50e-13 | 2.54e-01 | 0.067 |
84923 | FAM104A | LZE20T | Human | Esophagus | ESCC | 2.95e-03 | 1.03e-01 | 0.0662 |
84923 | FAM104A | LZE22T | Human | Esophagus | ESCC | 5.08e-03 | 3.68e-01 | 0.068 |
84923 | FAM104A | LZE24T | Human | Esophagus | ESCC | 5.51e-23 | 6.60e-01 | 0.0596 |
84923 | FAM104A | LZE21T | Human | Esophagus | ESCC | 7.94e-06 | 4.56e-01 | 0.0655 |
84923 | FAM104A | LZE6T | Human | Esophagus | ESCC | 3.80e-09 | 4.82e-01 | 0.0845 |
84923 | FAM104A | P1T-E | Human | Esophagus | ESCC | 1.52e-03 | 2.75e-01 | 0.0875 |
84923 | FAM104A | P2T-E | Human | Esophagus | ESCC | 4.61e-26 | 4.53e-01 | 0.1177 |
84923 | FAM104A | P4T-E | Human | Esophagus | ESCC | 3.30e-28 | 5.90e-01 | 0.1323 |
84923 | FAM104A | P5T-E | Human | Esophagus | ESCC | 1.92e-18 | 3.14e-01 | 0.1327 |
84923 | FAM104A | P8T-E | Human | Esophagus | ESCC | 3.37e-29 | 5.88e-01 | 0.0889 |
84923 | FAM104A | P9T-E | Human | Esophagus | ESCC | 2.19e-17 | 4.54e-01 | 0.1131 |
84923 | FAM104A | P10T-E | Human | Esophagus | ESCC | 9.02e-37 | 6.25e-01 | 0.116 |
84923 | FAM104A | P11T-E | Human | Esophagus | ESCC | 2.21e-19 | 7.64e-01 | 0.1426 |
84923 | FAM104A | P12T-E | Human | Esophagus | ESCC | 1.36e-27 | 5.31e-01 | 0.1122 |
84923 | FAM104A | P15T-E | Human | Esophagus | ESCC | 1.16e-32 | 7.65e-01 | 0.1149 |
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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 |
FAM104A | SNV | Missense_Mutation | c.349N>C | p.Glu117Gln | p.E117Q | Q969W3 | protein_coding | tolerated_low_confidence(0.06) | possibly_damaging(0.628) | TCGA-A2-A0YL-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cytoxan | SD | |
FAM104A | insertion | Frame_Shift_Ins | rs769947396 | c.268dupC | p.Gln90ProfsTer6 | p.Q90Pfs*6 | Q969W3 | protein_coding | TCGA-AN-A0FY-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
FAM104A | SNV | Missense_Mutation | novel | c.378N>G | p.Phe126Leu | p.F126L | Q969W3 | protein_coding | tolerated_low_confidence(0.65) | benign(0) | TCGA-C5-A2LZ-01 | Cervix | cervical & endocervical cancer | Female | >=65 | III/IV | Unknown | Unknown | PD |
FAM104A | SNV | Missense_Mutation | rs569512877 | c.155N>G | p.Ser52Cys | p.S52C | Q969W3 | protein_coding | tolerated_low_confidence(0.14) | benign(0.005) | TCGA-EK-A2RM-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
FAM104A | SNV | Missense_Mutation | novel | c.244N>A | p.Glu82Lys | p.E82K | Q969W3 | protein_coding | tolerated(0.16) | possibly_damaging(0.703) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
FAM104A | SNV | Missense_Mutation | rs777461616 | c.272N>T | p.Thr91Ile | p.T91I | Q969W3 | protein_coding | deleterious(0) | benign(0.382) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
FAM104A | SNV | Missense_Mutation | novel | c.344G>T | p.Ser115Ile | p.S115I | Q969W3 | protein_coding | deleterious_low_confidence(0) | benign(0.007) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
FAM104A | SNV | Missense_Mutation | rs768156778 | c.523G>A | p.Glu175Lys | p.E175K | Q969W3 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-AX-A2HC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | PD |
FAM104A | SNV | Missense_Mutation | c.374N>A | p.Ala125Glu | p.A125E | Q969W3 | protein_coding | deleterious_low_confidence(0.03) | benign(0.4) | TCGA-B5-A0K9-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
FAM104A | SNV | Missense_Mutation | rs749964305 | c.383C>T | p.Ala128Val | p.A128V | Q969W3 | protein_coding | tolerated_low_confidence(0.17) | benign(0.003) | TCGA-RC-A7SB-01 | Liver | liver hepatocellular carcinoma | Male | <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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