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Gene: DNAH17 |
Gene summary for DNAH17 |
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Gene information | Species | Human | Gene symbol | DNAH17 | Gene ID | 8632 |
Gene name | dynein axonemal heavy chain 17 | |
Gene Alias | DNAHL1 | |
Cytomap | 17q25.3 | |
Gene Type | protein-coding | GO ID | GO:0000226 | UniProtAcc | NA |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
8632 | DNAH17 | LZE4T | Human | Esophagus | ESCC | 2.37e-02 | 1.31e-01 | 0.0811 |
8632 | DNAH17 | LZE21T | Human | Esophagus | ESCC | 6.52e-03 | 2.77e-01 | 0.0655 |
8632 | DNAH17 | P2T-E | Human | Esophagus | ESCC | 4.16e-22 | 4.43e-01 | 0.1177 |
8632 | DNAH17 | P15T-E | Human | Esophagus | ESCC | 2.04e-07 | 2.20e-01 | 0.1149 |
8632 | DNAH17 | P17T-E | Human | Esophagus | ESCC | 1.49e-05 | 2.69e-01 | 0.1278 |
8632 | DNAH17 | P20T-E | Human | Esophagus | ESCC | 1.73e-12 | 3.47e-01 | 0.1124 |
8632 | DNAH17 | P21T-E | Human | Esophagus | ESCC | 3.75e-03 | 1.03e-01 | 0.1617 |
8632 | DNAH17 | P24T-E | Human | Esophagus | ESCC | 7.98e-13 | 3.55e-01 | 0.1287 |
8632 | DNAH17 | P27T-E | Human | Esophagus | ESCC | 8.84e-05 | 1.52e-01 | 0.1055 |
8632 | DNAH17 | P28T-E | Human | Esophagus | ESCC | 4.17e-05 | 1.40e-01 | 0.1149 |
8632 | DNAH17 | P31T-E | Human | Esophagus | ESCC | 6.56e-15 | 3.13e-01 | 0.1251 |
8632 | DNAH17 | P32T-E | Human | Esophagus | ESCC | 1.61e-32 | 6.26e-01 | 0.1666 |
8632 | DNAH17 | P36T-E | Human | Esophagus | ESCC | 7.95e-23 | 7.83e-01 | 0.1187 |
8632 | DNAH17 | P37T-E | Human | Esophagus | ESCC | 4.78e-22 | 5.83e-01 | 0.1371 |
8632 | DNAH17 | P40T-E | Human | Esophagus | ESCC | 8.35e-06 | 2.32e-01 | 0.109 |
8632 | DNAH17 | P42T-E | Human | Esophagus | ESCC | 2.62e-05 | 2.42e-01 | 0.1175 |
8632 | DNAH17 | P47T-E | Human | Esophagus | ESCC | 2.02e-06 | 1.66e-01 | 0.1067 |
8632 | DNAH17 | P49T-E | Human | Esophagus | ESCC | 7.97e-13 | 7.21e-01 | 0.1768 |
8632 | DNAH17 | P52T-E | Human | Esophagus | ESCC | 1.76e-12 | 2.37e-01 | 0.1555 |
8632 | DNAH17 | P62T-E | Human | Esophagus | ESCC | 1.85e-29 | 6.08e-01 | 0.1302 |
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Tissue | Expression Dynamics | Abbreviation |
Esophagus | ![]() | ESCC: Esophageal squamous cell carcinoma |
HGIN: High-grade intraepithelial neoplasias | ||
LGIN: Low-grade intraepithelial neoplasias |
∗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 |
hsa05014210 | Esophagus | ESCC | Amyotrophic lateral sclerosis | 266/4205 | 364/8465 | 1.31e-20 | 2.20e-18 | 1.13e-18 | 266 |
hsa05016210 | Esophagus | ESCC | Huntington disease | 226/4205 | 306/8465 | 1.38e-18 | 8.72e-17 | 4.46e-17 | 226 |
hsa05022210 | Esophagus | ESCC | Pathways of neurodegeneration - multiple diseases | 318/4205 | 476/8465 | 6.10e-15 | 2.04e-13 | 1.05e-13 | 318 |
hsa0501438 | Esophagus | ESCC | Amyotrophic lateral sclerosis | 266/4205 | 364/8465 | 1.31e-20 | 2.20e-18 | 1.13e-18 | 266 |
hsa0501638 | Esophagus | ESCC | Huntington disease | 226/4205 | 306/8465 | 1.38e-18 | 8.72e-17 | 4.46e-17 | 226 |
hsa0502238 | Esophagus | ESCC | Pathways of neurodegeneration - multiple diseases | 318/4205 | 476/8465 | 6.10e-15 | 2.04e-13 | 1.05e-13 | 318 |
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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 |
DNAH17 | SNV | Missense_Mutation | c.5082G>T | p.Gln1694His | p.Q1694H | Q9UFH2 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-CK-5916-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
DNAH17 | SNV | Missense_Mutation | rs370734377 | c.2741C>T | p.Pro914Leu | p.P914L | Q9UFH2 | protein_coding | deleterious(0.02) | probably_damaging(1) | TCGA-CK-5916-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
DNAH17 | SNV | Missense_Mutation | rs779503611 | c.9950N>T | p.Thr3317Met | p.T3317M | Q9UFH2 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-CM-4747-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | fluorouracil | SD |
DNAH17 | SNV | Missense_Mutation | rs769324928 | c.7312C>T | p.Arg2438Cys | p.R2438C | Q9UFH2 | protein_coding | tolerated(0.15) | probably_damaging(1) | TCGA-CM-5861-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
DNAH17 | SNV | Missense_Mutation | rs746227487 | c.12103N>A | p.Ala4035Thr | p.A4035T | Q9UFH2 | protein_coding | deleterious(0.02) | benign(0.113) | TCGA-D5-5537-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
DNAH17 | SNV | Missense_Mutation | rs371147513 | c.11153C>T | p.Thr3718Met | p.T3718M | Q9UFH2 | protein_coding | deleterious(0) | probably_damaging(0.958) | TCGA-D5-6540-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
DNAH17 | SNV | Missense_Mutation | rs753550278 | c.6094G>A | p.Gly2032Ser | p.G2032S | Q9UFH2 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-D5-6928-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
DNAH17 | SNV | Missense_Mutation | rs199512383 | c.10226N>T | p.Ala3409Val | p.A3409V | Q9UFH2 | protein_coding | deleterious(0.01) | probably_damaging(0.927) | TCGA-DM-A1HB-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD |
DNAH17 | SNV | Missense_Mutation | rs780254027 | c.850N>A | p.Asp284Asn | p.D284N | Q9UFH2 | protein_coding | deleterious(0.04) | benign(0.015) | TCGA-G4-6302-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
DNAH17 | SNV | Missense_Mutation | rs867799541 | c.877N>T | p.Arg293Trp | p.R293W | Q9UFH2 | protein_coding | deleterious(0.01) | possibly_damaging(0.651) | TCGA-G4-6628-01 | Colorectum | colon adenocarcinoma | 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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