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Gene: DNAH5 |
Gene summary for DNAH5 |
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Gene information | Species | Human | Gene symbol | DNAH5 | Gene ID | 1767 |
Gene name | dynein axonemal heavy chain 5 | |
Gene Alias | CILD3 | |
Cytomap | 5p15.2 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | Q8TE73 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
1767 | DNAH5 | C04 | Human | Oral cavity | OSCC | 2.09e-35 | 1.82e+00 | 0.2633 |
1767 | DNAH5 | C21 | Human | Oral cavity | OSCC | 7.14e-04 | 1.57e-01 | 0.2678 |
1767 | DNAH5 | SYSMH2 | Human | Oral cavity | OSCC | 4.32e-07 | 6.58e-01 | 0.2326 |
1767 | DNAH5 | SYSMH3 | Human | Oral cavity | OSCC | 5.39e-16 | 7.09e-01 | 0.2442 |
1767 | DNAH5 | SYSMH5 | Human | Oral cavity | OSCC | 1.09e-26 | 1.05e+00 | 0.0647 |
1767 | DNAH5 | HTA12-25-1 | Human | Pancreas | PDAC | 2.50e-03 | 4.72e-01 | 0.313 |
1767 | DNAH5 | HTA12-26-1 | Human | Pancreas | PDAC | 4.34e-14 | 7.27e-01 | 0.3728 |
1767 | DNAH5 | HTA12-29-1 | Human | Pancreas | PDAC | 6.09e-12 | 3.98e-01 | 0.3722 |
1767 | DNAH5 | HTA12-32-1 | Human | Pancreas | PDAC | 1.20e-02 | 7.98e-01 | 0.3624 |
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Tissue | Expression Dynamics | Abbreviation |
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 |
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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 |
GO:00991113 | Oral cavity | OSCC | microtubule-based transport | 96/7305 | 190/18723 | 7.92e-04 | 4.27e-03 | 96 |
GO:0021591 | Oral cavity | OSCC | ventricular system development | 18/7305 | 29/18723 | 1.00e-02 | 3.49e-02 | 18 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0501428 | Oral cavity | OSCC | Amyotrophic lateral sclerosis | 246/3704 | 364/8465 | 6.65e-21 | 1.11e-18 | 5.67e-19 | 246 |
hsa0501628 | Oral cavity | OSCC | Huntington disease | 204/3704 | 306/8465 | 1.70e-16 | 7.13e-15 | 3.63e-15 | 204 |
hsa0502228 | Oral cavity | OSCC | Pathways of neurodegeneration - multiple diseases | 292/3704 | 476/8465 | 1.60e-15 | 4.47e-14 | 2.28e-14 | 292 |
hsa05014112 | Oral cavity | OSCC | Amyotrophic lateral sclerosis | 246/3704 | 364/8465 | 6.65e-21 | 1.11e-18 | 5.67e-19 | 246 |
hsa05016112 | Oral cavity | OSCC | Huntington disease | 204/3704 | 306/8465 | 1.70e-16 | 7.13e-15 | 3.63e-15 | 204 |
hsa05022112 | Oral cavity | OSCC | Pathways of neurodegeneration - multiple diseases | 292/3704 | 476/8465 | 1.60e-15 | 4.47e-14 | 2.28e-14 | 292 |
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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 |
DNAH5 | SNV | Missense_Mutation | rs763286954 | c.13265N>C | p.Ile4422Thr | p.I4422T | Q8TE73 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-BR-4357-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | SD |
DNAH5 | SNV | Missense_Mutation | rs755574532 | c.233N>A | p.Arg78Gln | p.R78Q | Q8TE73 | protein_coding | tolerated(0.13) | benign(0.011) | TCGA-BR-4363-01 | Stomach | stomach adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
DNAH5 | SNV | Missense_Mutation | rs755574532 | c.233N>A | p.Arg78Gln | p.R78Q | Q8TE73 | protein_coding | tolerated(0.13) | benign(0.011) | TCGA-BR-4368-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
DNAH5 | SNV | Missense_Mutation | c.11554N>T | p.Asp3852Tyr | p.D3852Y | Q8TE73 | protein_coding | deleterious(0) | possibly_damaging(0.872) | TCGA-BR-6452-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
DNAH5 | SNV | Missense_Mutation | c.10349N>G | p.Glu3450Gly | p.E3450G | Q8TE73 | protein_coding | tolerated(0.16) | benign(0.315) | TCGA-BR-6452-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
DNAH5 | SNV | Missense_Mutation | rs781356156 | c.532N>A | p.Ala178Thr | p.A178T | Q8TE73 | protein_coding | tolerated(0.19) | benign(0.003) | TCGA-BR-6454-01 | Stomach | stomach adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
DNAH5 | SNV | Missense_Mutation | c.11783N>C | p.Lys3928Thr | p.K3928T | Q8TE73 | protein_coding | deleterious(0.01) | possibly_damaging(0.716) | TCGA-BR-6458-01 | Stomach | stomach adenocarcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | PD | |
DNAH5 | SNV | Missense_Mutation | c.11034N>C | p.Lys3678Asn | p.K3678N | Q8TE73 | protein_coding | tolerated(0.05) | possibly_damaging(0.627) | TCGA-BR-6458-01 | Stomach | stomach adenocarcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | PD | |
DNAH5 | SNV | Missense_Mutation | c.13631G>A | p.Gly4544Asp | p.G4544D | Q8TE73 | protein_coding | deleterious(0.02) | possibly_damaging(0.783) | TCGA-BR-6566-01 | Stomach | stomach adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
DNAH5 | SNV | Missense_Mutation | novel | c.13368N>A | p.Phe4456Leu | p.F4456L | Q8TE73 | protein_coding | tolerated(0.06) | benign(0.313) | TCGA-BR-7196-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | etoposide | 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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