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Gene: DNAAF5 |
Gene summary for DNAAF5 |
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Gene information | Species | Human | Gene symbol | DNAAF5 | Gene ID | 54919 |
Gene name | dynein axonemal assembly factor 5 | |
Gene Alias | CILD18 | |
Cytomap | 7p22.3 | |
Gene Type | protein-coding | GO ID | GO:0000226 | UniProtAcc | B3KPE2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
54919 | DNAAF5 | LZE2T | Human | Esophagus | ESCC | 1.87e-03 | 3.90e-01 | 0.082 |
54919 | DNAAF5 | LZE22T | Human | Esophagus | ESCC | 1.54e-07 | 3.64e-01 | 0.068 |
54919 | DNAAF5 | LZE24T | Human | Esophagus | ESCC | 1.43e-02 | 1.10e-01 | 0.0596 |
54919 | DNAAF5 | P1T-E | Human | Esophagus | ESCC | 8.80e-03 | 3.23e-01 | 0.0875 |
54919 | DNAAF5 | P2T-E | Human | Esophagus | ESCC | 5.34e-29 | 4.99e-01 | 0.1177 |
54919 | DNAAF5 | P4T-E | Human | Esophagus | ESCC | 3.78e-09 | 2.10e-01 | 0.1323 |
54919 | DNAAF5 | P5T-E | Human | Esophagus | ESCC | 6.91e-06 | 1.44e-01 | 0.1327 |
54919 | DNAAF5 | P8T-E | Human | Esophagus | ESCC | 2.34e-07 | 1.67e-01 | 0.0889 |
54919 | DNAAF5 | P9T-E | Human | Esophagus | ESCC | 2.65e-07 | 2.28e-01 | 0.1131 |
54919 | DNAAF5 | P10T-E | Human | Esophagus | ESCC | 1.30e-08 | 1.43e-01 | 0.116 |
54919 | DNAAF5 | P11T-E | Human | Esophagus | ESCC | 3.83e-02 | 2.12e-01 | 0.1426 |
54919 | DNAAF5 | P12T-E | Human | Esophagus | ESCC | 2.52e-03 | 1.20e-01 | 0.1122 |
54919 | DNAAF5 | P15T-E | Human | Esophagus | ESCC | 3.56e-07 | 2.06e-01 | 0.1149 |
54919 | DNAAF5 | P16T-E | Human | Esophagus | ESCC | 5.22e-08 | 1.65e-01 | 0.1153 |
54919 | DNAAF5 | P17T-E | Human | Esophagus | ESCC | 3.84e-04 | 2.44e-01 | 0.1278 |
54919 | DNAAF5 | P20T-E | Human | Esophagus | ESCC | 9.32e-09 | 2.25e-01 | 0.1124 |
54919 | DNAAF5 | P21T-E | Human | Esophagus | ESCC | 3.97e-12 | 2.90e-01 | 0.1617 |
54919 | DNAAF5 | P22T-E | Human | Esophagus | ESCC | 3.87e-04 | 1.07e-01 | 0.1236 |
54919 | DNAAF5 | P23T-E | Human | Esophagus | ESCC | 3.28e-03 | 1.38e-01 | 0.108 |
54919 | DNAAF5 | P24T-E | Human | Esophagus | ESCC | 2.70e-04 | 1.34e-01 | 0.1287 |
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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 |
DNAAF5 | SNV | Missense_Mutation | novel | c.2419N>A | p.Asp807Asn | p.D807N | Q86Y56 | protein_coding | tolerated(0.24) | benign(0.038) | TCGA-5L-AAT0-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD |
DNAAF5 | SNV | Missense_Mutation | novel | c.898N>C | p.Glu300Gln | p.E300Q | Q86Y56 | protein_coding | deleterious(0) | probably_damaging(0.976) | TCGA-A2-A0YH-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | SD |
DNAAF5 | SNV | Missense_Mutation | novel | c.949C>A | p.Gln317Lys | p.Q317K | Q86Y56 | protein_coding | deleterious(0.01) | benign(0.214) | TCGA-BH-A0C0-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | SD |
DNAAF5 | SNV | Missense_Mutation | rs773744343 | c.1507N>T | p.Ala503Ser | p.A503S | Q86Y56 | protein_coding | tolerated(0.21) | benign(0.009) | TCGA-C8-A26X-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | CR |
DNAAF5 | SNV | Missense_Mutation | c.2311C>G | p.Leu771Val | p.L771V | Q86Y56 | protein_coding | deleterious(0.01) | possibly_damaging(0.902) | TCGA-EW-A1IZ-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | taxotere | SD | |
DNAAF5 | SNV | Missense_Mutation | c.2417N>C | p.Gln806Pro | p.Q806P | Q86Y56 | protein_coding | deleterious(0) | probably_damaging(0.98) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
DNAAF5 | SNV | Missense_Mutation | c.2366A>G | p.Tyr789Cys | p.Y789C | Q86Y56 | protein_coding | tolerated(0.11) | possibly_damaging(0.49) | TCGA-G4-6588-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
DNAAF5 | SNV | Missense_Mutation | novel | c.2081N>G | p.Gln694Arg | p.Q694R | Q86Y56 | protein_coding | tolerated(0.11) | benign(0.218) | TCGA-AG-3584-01 | Colorectum | rectum adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folinic | PD |
DNAAF5 | SNV | Missense_Mutation | rs534027051 | c.1714G>A | p.Ala572Thr | p.A572T | Q86Y56 | protein_coding | tolerated(0.32) | benign(0.127) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
DNAAF5 | SNV | Missense_Mutation | rs749838774 | c.829N>T | p.Arg277Cys | p.R277C | Q86Y56 | protein_coding | deleterious(0) | possibly_damaging(0.891) | TCGA-AP-A1DV-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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