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Gene: DNAH11 |
Gene summary for DNAH11 |
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Gene information | Species | Human | Gene symbol | DNAH11 | Gene ID | 8701 |
Gene name | dynein axonemal heavy chain 11 | |
Gene Alias | CILD7 | |
Cytomap | 7p15.3 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | H9NAJ7 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
8701 | DNAH11 | AEH-subject1 | Human | Endometrium | AEH | 3.74e-02 | 1.75e-01 | -0.3059 |
8701 | DNAH11 | AEH-subject2 | Human | Endometrium | AEH | 5.92e-04 | 2.57e-01 | -0.2525 |
8701 | DNAH11 | AEH-subject3 | Human | Endometrium | AEH | 6.96e-06 | 2.81e-01 | -0.2576 |
8701 | DNAH11 | AEH-subject4 | Human | Endometrium | AEH | 4.55e-26 | 8.06e-01 | -0.2657 |
8701 | DNAH11 | AEH-subject5 | Human | Endometrium | AEH | 3.66e-08 | 3.57e-01 | -0.2953 |
8701 | DNAH11 | EEC-subject2 | Human | Endometrium | EEC | 2.45e-20 | 5.66e-01 | -0.2607 |
8701 | DNAH11 | EEC-subject4 | Human | Endometrium | EEC | 6.28e-04 | 3.10e-01 | -0.2571 |
8701 | DNAH11 | TD9 | Human | Lung | IAC | 1.26e-09 | 1.01e+00 | 0.088 |
8701 | DNAH11 | RNA-P17T-P17T-4 | Human | Lung | IAC | 4.28e-05 | 7.75e-01 | 0.343 |
8701 | DNAH11 | RNA-P17T-P17T-6 | Human | Lung | IAC | 1.48e-03 | 5.29e-01 | 0.3385 |
8701 | DNAH11 | RNA-P17T-P17T-8 | Human | Lung | IAC | 4.12e-03 | 4.94e-01 | 0.3329 |
8701 | DNAH11 | RNA-P3T-P3T-1 | Human | Lung | IAC | 1.35e-14 | 8.50e-01 | 0.1829 |
8701 | DNAH11 | RNA-P3T-P3T-2 | Human | Lung | IAC | 4.73e-12 | 7.71e-01 | 0.1835 |
8701 | DNAH11 | RNA-P3T-P3T-4 | Human | Lung | IAC | 1.04e-14 | 8.64e-01 | 0.1859 |
8701 | DNAH11 | RNA-P6T1-P6T1-1 | Human | Lung | MIAC | 2.66e-09 | 1.15e+00 | -0.0238 |
8701 | DNAH11 | RNA-P6T1-P6T1-2 | Human | Lung | MIAC | 5.44e-06 | 9.27e-01 | -0.0186 |
8701 | DNAH11 | RNA-P6T1-P6T1-3 | Human | Lung | MIAC | 6.04e-07 | 1.03e+00 | -0.0296 |
8701 | DNAH11 | RNA-P6T1-P6T1-4 | Human | Lung | MIAC | 1.92e-13 | 1.22e+00 | -0.0263 |
8701 | DNAH11 | RNA-P6T2-P6T2-2 | Human | Lung | IAC | 3.12e-03 | 2.00e-01 | -0.0132 |
8701 | DNAH11 | RNA-P7T1-P7T1-1 | Human | Lung | AIS | 2.37e-02 | 4.39e-01 | -0.0961 |
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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 |
GO:00030072 | Endometrium | AEH | heart morphogenesis | 45/2100 | 246/18723 | 6.41e-04 | 6.23e-03 | 45 |
GO:00032062 | Endometrium | AEH | cardiac chamber morphogenesis | 23/2100 | 121/18723 | 7.76e-03 | 4.33e-02 | 23 |
GO:00030071 | Endometrium | EEC | heart morphogenesis | 45/2168 | 246/18723 | 1.24e-03 | 1.03e-02 | 45 |
GO:0099111 | Lung | IAC | microtubule-based transport | 35/2061 | 190/18723 | 1.55e-03 | 1.64e-02 | 35 |
GO:00328861 | Lung | MIAC | regulation of microtubule-based process | 23/967 | 240/18723 | 3.27e-03 | 4.31e-02 | 23 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0501620 | Endometrium | AEH | Huntington disease | 118/1197 | 306/8465 | 3.00e-27 | 2.44e-25 | 1.78e-25 | 118 |
hsa0501420 | Endometrium | AEH | Amyotrophic lateral sclerosis | 123/1197 | 364/8465 | 2.17e-22 | 7.82e-21 | 5.72e-21 | 123 |
hsa0502220 | Endometrium | AEH | Pathways of neurodegeneration - multiple diseases | 137/1197 | 476/8465 | 9.27e-18 | 2.32e-16 | 1.70e-16 | 137 |
hsa048144 | Endometrium | AEH | Motor proteins | 42/1197 | 193/8465 | 2.41e-03 | 1.42e-02 | 1.04e-02 | 42 |
hsa05016110 | Endometrium | AEH | Huntington disease | 118/1197 | 306/8465 | 3.00e-27 | 2.44e-25 | 1.78e-25 | 118 |
hsa05014110 | Endometrium | AEH | Amyotrophic lateral sclerosis | 123/1197 | 364/8465 | 2.17e-22 | 7.82e-21 | 5.72e-21 | 123 |
hsa05022110 | Endometrium | AEH | Pathways of neurodegeneration - multiple diseases | 137/1197 | 476/8465 | 9.27e-18 | 2.32e-16 | 1.70e-16 | 137 |
hsa0481411 | Endometrium | AEH | Motor proteins | 42/1197 | 193/8465 | 2.41e-03 | 1.42e-02 | 1.04e-02 | 42 |
hsa0501625 | Endometrium | EEC | Huntington disease | 120/1237 | 306/8465 | 3.86e-27 | 4.23e-25 | 3.15e-25 | 120 |
hsa0501425 | Endometrium | EEC | Amyotrophic lateral sclerosis | 128/1237 | 364/8465 | 9.83e-24 | 4.04e-22 | 3.01e-22 | 128 |
hsa0502225 | Endometrium | EEC | Pathways of neurodegeneration - multiple diseases | 140/1237 | 476/8465 | 9.49e-18 | 2.60e-16 | 1.94e-16 | 140 |
hsa048142 | Endometrium | EEC | Motor proteins | 42/1237 | 193/8465 | 4.43e-03 | 2.39e-02 | 1.78e-02 | 42 |
hsa0501635 | Endometrium | EEC | Huntington disease | 120/1237 | 306/8465 | 3.86e-27 | 4.23e-25 | 3.15e-25 | 120 |
hsa0501435 | Endometrium | EEC | Amyotrophic lateral sclerosis | 128/1237 | 364/8465 | 9.83e-24 | 4.04e-22 | 3.01e-22 | 128 |
hsa0502235 | Endometrium | EEC | Pathways of neurodegeneration - multiple diseases | 140/1237 | 476/8465 | 9.49e-18 | 2.60e-16 | 1.94e-16 | 140 |
hsa048143 | Endometrium | EEC | Motor proteins | 42/1237 | 193/8465 | 4.43e-03 | 2.39e-02 | 1.78e-02 | 42 |
hsa04814 | Lung | MIAC | Motor proteins | 21/507 | 193/8465 | 5.64e-03 | 3.82e-02 | 2.76e-02 | 21 |
hsa048141 | Lung | MIAC | Motor proteins | 21/507 | 193/8465 | 5.64e-03 | 3.82e-02 | 2.76e-02 | 21 |
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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 |
DNAH11 | SNV | Missense_Mutation | c.4126N>T | p.Val1376Phe | p.V1376F | Q96DT5 | protein_coding | tolerated(0.05) | benign(0.007) | TCGA-AF-3913-01 | Colorectum | rectum adenocarcinoma | Male | <65 | III/IV | Chemotherapy | xeloda | PD | |
DNAH11 | SNV | Missense_Mutation | rs727502969 | c.10441N>A | p.Glu3481Lys | p.E3481K | Q96DT5 | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-AG-3728-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | folinic | CR |
DNAH11 | SNV | Missense_Mutation | novel | c.1900N>C | p.Asn634His | p.N634H | Q96DT5 | protein_coding | tolerated(0.09) | benign(0.067) | TCGA-AG-3892-01 | Colorectum | rectum adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
DNAH11 | SNV | Missense_Mutation | novel | c.3270N>C | p.Glu1090Asp | p.E1090D | Q96DT5 | protein_coding | tolerated(0.06) | probably_damaging(0.922) | TCGA-AG-3892-01 | Colorectum | rectum adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
DNAH11 | SNV | Missense_Mutation | c.9346N>A | p.Leu3116Ile | p.L3116I | Q96DT5 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AG-3892-01 | Colorectum | rectum adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
DNAH11 | SNV | Missense_Mutation | c.5908N>G | p.Arg1970Gly | p.R1970G | Q96DT5 | protein_coding | deleterious(0.01) | probably_damaging(0.959) | TCGA-AG-4005-01 | Colorectum | rectum adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folinic | CR | |
DNAH11 | SNV | Missense_Mutation | c.1978T>G | p.Leu660Val | p.L660V | Q96DT5 | protein_coding | tolerated(0.15) | benign(0.007) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
DNAH11 | SNV | Missense_Mutation | c.3292A>G | p.Lys1098Glu | p.K1098E | Q96DT5 | protein_coding | tolerated(0.58) | benign(0.091) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
DNAH11 | SNV | Missense_Mutation | c.5368G>A | p.Glu1790Lys | p.E1790K | Q96DT5 | protein_coding | tolerated(0.18) | possibly_damaging(0.89) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
DNAH11 | SNV | Missense_Mutation | c.10932T>G | p.Ile3644Met | p.I3644M | Q96DT5 | protein_coding | deleterious(0) | probably_damaging(0.952) | TCGA-AG-A002-01 | Colorectum | rectum 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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