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Gene: HAUS1 |
Gene summary for HAUS1 |
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Gene information | Species | Human | Gene symbol | HAUS1 | Gene ID | 115106 |
Gene name | HAUS augmin like complex subunit 1 | |
Gene Alias | CCDC5 | |
Cytomap | 18q21.1 | |
Gene Type | protein-coding | GO ID | GO:0000226 | UniProtAcc | Q96CS2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
115106 | HAUS1 | C06 | Human | Oral cavity | OSCC | 1.04e-05 | 8.56e-01 | 0.2699 |
115106 | HAUS1 | C08 | Human | Oral cavity | OSCC | 3.34e-23 | 7.11e-01 | 0.1919 |
115106 | HAUS1 | LN22 | Human | Oral cavity | OSCC | 6.23e-09 | 9.82e-01 | 0.1733 |
115106 | HAUS1 | LN38 | Human | Oral cavity | OSCC | 7.14e-03 | 8.75e-01 | 0.168 |
115106 | HAUS1 | LN46 | Human | Oral cavity | OSCC | 4.75e-25 | 8.06e-01 | 0.1666 |
115106 | HAUS1 | LP15 | Human | Oral cavity | LP | 1.54e-03 | 7.01e-01 | 0.2174 |
115106 | HAUS1 | LP17 | Human | Oral cavity | LP | 7.00e-07 | 6.61e-01 | 0.2349 |
115106 | HAUS1 | SYSMH2 | Human | Oral cavity | OSCC | 1.27e-10 | 4.07e-01 | 0.2326 |
115106 | HAUS1 | SYSMH3 | Human | Oral cavity | OSCC | 2.69e-10 | 4.25e-01 | 0.2442 |
115106 | HAUS1 | P1_cSCC | Human | Skin | cSCC | 1.55e-23 | 7.70e-01 | 0.0292 |
115106 | HAUS1 | P2_cSCC | Human | Skin | cSCC | 4.48e-22 | 5.79e-01 | -0.024 |
115106 | HAUS1 | P4_cSCC | Human | Skin | cSCC | 1.47e-34 | 8.42e-01 | -0.00290000000000005 |
115106 | HAUS1 | P10_cSCC | Human | Skin | cSCC | 1.99e-44 | 1.04e+00 | 0.1017 |
115106 | HAUS1 | male-WTA | Human | Thyroid | PTC | 1.22e-08 | 4.45e-02 | 0.1037 |
115106 | HAUS1 | PTC01 | Human | Thyroid | PTC | 1.68e-07 | 4.58e-02 | 0.1899 |
115106 | HAUS1 | PTC05 | Human | Thyroid | PTC | 2.68e-06 | 1.94e-01 | 0.2065 |
115106 | HAUS1 | PTC06 | Human | Thyroid | PTC | 8.70e-13 | 2.34e-01 | 0.2057 |
115106 | HAUS1 | PTC07 | Human | Thyroid | PTC | 9.34e-09 | 1.21e-01 | 0.2044 |
115106 | HAUS1 | ATC13 | Human | Thyroid | ATC | 2.67e-17 | 2.84e-01 | 0.34 |
115106 | HAUS1 | ATC2 | Human | Thyroid | ATC | 3.99e-09 | 6.78e-01 | 0.34 |
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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:000705114 | Esophagus | ESCC | spindle organization | 134/8552 | 184/18723 | 5.70e-14 | 2.87e-12 | 134 |
GO:00512256 | Esophagus | ESCC | spindle assembly | 85/8552 | 117/18723 | 2.72e-09 | 5.98e-08 | 85 |
GO:00070982 | Esophagus | ESCC | centrosome cycle | 85/8552 | 130/18723 | 4.41e-06 | 4.69e-05 | 85 |
GO:00310233 | Esophagus | ESCC | microtubule organizing center organization | 92/8552 | 143/18723 | 5.04e-06 | 5.31e-05 | 92 |
GO:00070517 | Oral cavity | OSCC | spindle organization | 117/7305 | 184/18723 | 1.16e-11 | 4.17e-10 | 117 |
GO:00512255 | Oral cavity | OSCC | spindle assembly | 73/7305 | 117/18723 | 2.51e-07 | 3.96e-06 | 73 |
GO:00070981 | Oral cavity | OSCC | centrosome cycle | 66/7305 | 130/18723 | 4.17e-03 | 1.70e-02 | 66 |
GO:00310232 | Oral cavity | OSCC | microtubule organizing center organization | 70/7305 | 143/18723 | 9.71e-03 | 3.44e-02 | 70 |
GO:000705113 | Oral cavity | LP | spindle organization | 72/4623 | 184/18723 | 9.67e-06 | 1.78e-04 | 72 |
GO:005122512 | Oral cavity | LP | spindle assembly | 42/4623 | 117/18723 | 4.39e-03 | 2.80e-02 | 42 |
GO:000705115 | Skin | cSCC | spindle organization | 96/4864 | 184/18723 | 2.59e-14 | 1.77e-12 | 96 |
GO:005122513 | Skin | cSCC | spindle assembly | 60/4864 | 117/18723 | 4.15e-09 | 1.41e-07 | 60 |
GO:00310234 | Skin | cSCC | microtubule organizing center organization | 58/4864 | 143/18723 | 9.47e-05 | 8.83e-04 | 58 |
GO:00070983 | Skin | cSCC | centrosome cycle | 53/4864 | 130/18723 | 1.59e-04 | 1.39e-03 | 53 |
GO:000705116 | Thyroid | PTC | spindle organization | 92/5968 | 184/18723 | 2.21e-07 | 3.92e-06 | 92 |
GO:005122514 | Thyroid | PTC | spindle assembly | 56/5968 | 117/18723 | 2.17e-04 | 1.60e-03 | 56 |
GO:00310235 | Thyroid | PTC | microtubule organizing center organization | 65/5968 | 143/18723 | 4.48e-04 | 2.96e-03 | 65 |
GO:00070984 | Thyroid | PTC | centrosome cycle | 59/5968 | 130/18723 | 8.39e-04 | 5.16e-03 | 59 |
GO:000705122 | Thyroid | ATC | spindle organization | 109/6293 | 184/18723 | 7.99e-13 | 3.46e-11 | 109 |
GO:005122521 | Thyroid | ATC | spindle assembly | 66/6293 | 117/18723 | 3.28e-07 | 4.88e-06 | 66 |
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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 |
HAUS1 | SNV | Missense_Mutation | c.148G>T | p.Asp50Tyr | p.D50Y | Q96CS2 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-A8-A079-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | 5-fluorouracil | SD | |
HAUS1 | SNV | Missense_Mutation | novel | c.454N>C | p.Val152Leu | p.V152L | Q96CS2 | protein_coding | tolerated(0.08) | benign(0.015) | TCGA-AR-A256-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | PD |
HAUS1 | SNV | Missense_Mutation | c.705G>T | p.Lys235Asn | p.K235N | Q96CS2 | protein_coding | deleterious(0.02) | probably_damaging(0.956) | TCGA-FU-A3HZ-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
HAUS1 | SNV | Missense_Mutation | c.732N>T | p.Leu244Phe | p.L244F | Q96CS2 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AA-3715-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
HAUS1 | SNV | Missense_Mutation | c.61N>A | p.Asp21Asn | p.D21N | Q96CS2 | protein_coding | tolerated(0.37) | benign(0.027) | TCGA-AA-3811-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD | |
HAUS1 | SNV | Missense_Mutation | rs766441279 | c.95N>A | p.Arg32Gln | p.R32Q | Q96CS2 | protein_coding | tolerated(0.07) | benign(0.308) | TCGA-AZ-6601-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
HAUS1 | SNV | Missense_Mutation | c.146N>T | p.Arg49Met | p.R49M | Q96CS2 | protein_coding | deleterious(0) | probably_damaging(0.947) | TCGA-CK-6746-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
HAUS1 | SNV | Missense_Mutation | rs769854055 | c.743C>T | p.Pro248Leu | p.P248L | Q96CS2 | protein_coding | tolerated(0.13) | benign(0.073) | TCGA-D5-6928-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
HAUS1 | SNV | Missense_Mutation | rs570163326 | c.533N>A | p.Arg178His | p.R178H | Q96CS2 | protein_coding | tolerated(0.13) | benign(0.031) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
HAUS1 | SNV | Missense_Mutation | c.521N>C | p.Lys174Thr | p.K174T | Q96CS2 | protein_coding | tolerated(0.09) | benign(0.109) | TCGA-AP-A056-01 | 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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