|
Gene: HAUS2 |
Gene summary for HAUS2 |
Gene summary. |
Gene information | Species | Human | Gene symbol | HAUS2 | Gene ID | 55142 |
Gene name | HAUS augmin like complex subunit 2 | |
Gene Alias | C15orf25 | |
Cytomap | 15q15.2 | |
Gene Type | protein-coding | GO ID | GO:0000226 | UniProtAcc | Q9NVX0 |
Top |
Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
55142 | HAUS2 | P52T-E | Human | Esophagus | ESCC | 2.24e-28 | 5.69e-01 | 0.1555 |
55142 | HAUS2 | P54T-E | Human | Esophagus | ESCC | 7.03e-09 | 2.37e-01 | 0.0975 |
55142 | HAUS2 | P56T-E | Human | Esophagus | ESCC | 2.38e-05 | 6.30e-01 | 0.1613 |
55142 | HAUS2 | P57T-E | Human | Esophagus | ESCC | 1.90e-11 | 1.40e-01 | 0.0926 |
55142 | HAUS2 | P61T-E | Human | Esophagus | ESCC | 8.38e-08 | 2.17e-01 | 0.099 |
55142 | HAUS2 | P62T-E | Human | Esophagus | ESCC | 7.52e-19 | 2.65e-01 | 0.1302 |
55142 | HAUS2 | P65T-E | Human | Esophagus | ESCC | 1.87e-12 | 1.71e-01 | 0.0978 |
55142 | HAUS2 | P74T-E | Human | Esophagus | ESCC | 2.62e-17 | 4.88e-01 | 0.1479 |
55142 | HAUS2 | P75T-E | Human | Esophagus | ESCC | 1.86e-35 | 6.32e-01 | 0.1125 |
55142 | HAUS2 | P76T-E | Human | Esophagus | ESCC | 8.33e-17 | 3.39e-01 | 0.1207 |
55142 | HAUS2 | P79T-E | Human | Esophagus | ESCC | 1.51e-16 | 2.31e-01 | 0.1154 |
55142 | HAUS2 | P80T-E | Human | Esophagus | ESCC | 6.44e-21 | 4.43e-01 | 0.155 |
55142 | HAUS2 | P82T-E | Human | Esophagus | ESCC | 6.12e-08 | 3.46e-01 | 0.1072 |
55142 | HAUS2 | P83T-E | Human | Esophagus | ESCC | 6.87e-23 | 7.38e-01 | 0.1738 |
55142 | HAUS2 | P84T-E | Human | Esophagus | ESCC | 2.55e-07 | 3.20e-01 | 0.0933 |
55142 | HAUS2 | P89T-E | Human | Esophagus | ESCC | 1.20e-05 | 6.26e-01 | 0.1752 |
55142 | HAUS2 | P91T-E | Human | Esophagus | ESCC | 8.96e-10 | 1.12e+00 | 0.1828 |
55142 | HAUS2 | P107T-E | Human | Esophagus | ESCC | 2.16e-47 | 1.09e+00 | 0.171 |
55142 | HAUS2 | P126T-E | Human | Esophagus | ESCC | 4.43e-09 | 5.85e-01 | 0.1125 |
55142 | HAUS2 | P127T-E | Human | Esophagus | ESCC | 1.75e-10 | 2.14e-01 | 0.0826 |
Page: 1 2 3 4 5 |
Transcriptomic changes along malignancy continuum. |
∗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. |
Top |
Malignant transformation related pathway analysis |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
Figure of enriched GO biological processes. |
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). |
Page: 1 2 3 4 5 6 7 8 9 |
Enriched GO biological processes. |
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:0051258111 | Esophagus | ESCC | protein polymerization | 183/8552 | 297/18723 | 1.94e-08 | 3.75e-07 | 183 |
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:00311094 | Esophagus | ESCC | microtubule polymerization or depolymerization | 77/8552 | 122/18723 | 7.60e-05 | 5.68e-04 | 77 |
GO:00467856 | Esophagus | ESCC | microtubule polymerization | 55/8552 | 83/18723 | 1.21e-04 | 8.31e-04 | 55 |
GO:00070205 | Esophagus | ESCC | microtubule nucleation | 27/8552 | 35/18723 | 1.48e-04 | 9.88e-04 | 27 |
GO:005125822 | Liver | HCC | protein polymerization | 182/7958 | 297/18723 | 4.17e-11 | 1.58e-09 | 182 |
GO:000705111 | Liver | HCC | spindle organization | 116/7958 | 184/18723 | 1.40e-08 | 3.40e-07 | 116 |
GO:005122511 | Liver | HCC | spindle assembly | 75/7958 | 117/18723 | 1.92e-06 | 2.67e-05 | 75 |
GO:0031023 | Liver | HCC | microtubule organizing center organization | 82/7958 | 143/18723 | 2.38e-04 | 1.79e-03 | 82 |
GO:0007098 | Liver | HCC | centrosome cycle | 75/7958 | 130/18723 | 3.33e-04 | 2.34e-03 | 75 |
GO:0046785 | Liver | HCC | microtubule polymerization | 51/7958 | 83/18723 | 3.82e-04 | 2.61e-03 | 51 |
GO:0007020 | Liver | HCC | microtubule nucleation | 25/7958 | 35/18723 | 5.05e-04 | 3.29e-03 | 25 |
GO:0031109 | Liver | HCC | microtubule polymerization or depolymerization | 68/7958 | 122/18723 | 2.14e-03 | 1.08e-02 | 68 |
GO:00070517 | Oral cavity | OSCC | spindle organization | 117/7305 | 184/18723 | 1.16e-11 | 4.17e-10 | 117 |
GO:005125820 | Oral cavity | OSCC | protein polymerization | 169/7305 | 297/18723 | 2.57e-10 | 7.17e-09 | 169 |
GO:00512255 | Oral cavity | OSCC | spindle assembly | 73/7305 | 117/18723 | 2.51e-07 | 3.96e-06 | 73 |
GO:00070204 | Oral cavity | OSCC | microtubule nucleation | 28/7305 | 35/18723 | 8.71e-07 | 1.19e-05 | 28 |
Page: 1 2 |
Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
Page: 1 |
Top |
Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
Top |
Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
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. |
Page: 1 |
Top |
Somatic mutation of malignant transformation related genes |
Annotation of somatic variants for genes involved in malignant transformation |
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 |
HAUS2 | SNV | Missense_Mutation | c.539C>T | p.Thr180Ile | p.T180I | Q9NVX0 | protein_coding | tolerated(0.56) | benign(0.391) | TCGA-BH-A0HF-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD | |
HAUS2 | SNV | Missense_Mutation | c.315N>C | p.Glu105Asp | p.E105D | Q9NVX0 | protein_coding | deleterious(0.03) | benign(0.021) | TCGA-EK-A2PG-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
HAUS2 | SNV | Missense_Mutation | c.373N>A | p.Glu125Lys | p.E125K | Q9NVX0 | protein_coding | tolerated(0.05) | possibly_damaging(0.88) | TCGA-EK-A3GM-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
HAUS2 | SNV | Missense_Mutation | c.535N>C | p.Glu179Gln | p.E179Q | Q9NVX0 | protein_coding | deleterious(0) | benign(0.439) | TCGA-Q1-A5R2-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | PR | |
HAUS2 | SNV | Missense_Mutation | novel | c.125N>A | p.Ser42Tyr | p.S42Y | Q9NVX0 | protein_coding | deleterious(0) | benign(0.246) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
HAUS2 | SNV | Missense_Mutation | novel | c.617N>T | p.Ala206Val | p.A206V | Q9NVX0 | protein_coding | tolerated_low_confidence(0.05) | benign(0.178) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
HAUS2 | SNV | Missense_Mutation | rs777814162 | c.572G>A | p.Arg191His | p.R191H | Q9NVX0 | protein_coding | deleterious(0) | possibly_damaging(0.783) | TCGA-A5-A0VP-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
HAUS2 | SNV | Missense_Mutation | novel | c.648N>G | p.Ile216Met | p.I216M | Q9NVX0 | protein_coding | tolerated_low_confidence(0.05) | possibly_damaging(0.487) | TCGA-AJ-A3EL-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
HAUS2 | SNV | Missense_Mutation | novel | c.643G>T | p.Asp215Tyr | p.D215Y | Q9NVX0 | protein_coding | deleterious_low_confidence(0) | benign(0.006) | TCGA-AP-A1E0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | SD |
HAUS2 | SNV | Missense_Mutation | c.236N>C | p.Val79Ala | p.V79A | Q9NVX0 | protein_coding | deleterious(0) | benign(0.115) | TCGA-AX-A0J1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
Page: 1 2 3 |
Top |
Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
Page: 1 |