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Gene: SNHG32 |
Gene summary for SNHG32 |
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Gene information | Species | Human | Gene symbol | SNHG32 | Gene ID | 50854 |
Gene name | small nucleolar RNA host gene 32 | |
Gene Alias | C6orf48 | |
Cytomap | 6p21.33 | |
Gene Type | ncRNA | GO ID | NA | 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 |
50854 | SNHG32 | sample1 | Human | Cervix | CC | 3.67e-07 | 2.44e-01 | 0.0959 |
50854 | SNHG32 | sample3 | Human | Cervix | CC | 1.02e-16 | 2.58e-01 | 0.1387 |
50854 | SNHG32 | H2 | Human | Cervix | HSIL_HPV | 8.42e-11 | 2.05e-01 | 0.0632 |
50854 | SNHG32 | T1 | Human | Cervix | CC | 2.35e-17 | 3.47e-01 | 0.0918 |
50854 | SNHG32 | T2 | Human | Cervix | CC | 4.20e-19 | 5.86e-01 | 0.0709 |
50854 | SNHG32 | T3 | Human | Cervix | CC | 3.12e-19 | 2.92e-01 | 0.1389 |
50854 | SNHG32 | HTA11_3410_2000001011 | Human | Colorectum | AD | 7.99e-40 | 7.20e-01 | 0.0155 |
50854 | SNHG32 | HTA11_2487_2000001011 | Human | Colorectum | SER | 2.86e-10 | 3.24e-01 | -0.1808 |
50854 | SNHG32 | HTA11_2951_2000001011 | Human | Colorectum | AD | 3.35e-17 | 7.57e-01 | 0.0216 |
50854 | SNHG32 | HTA11_1938_2000001011 | Human | Colorectum | AD | 6.92e-17 | 4.41e-01 | -0.0811 |
50854 | SNHG32 | HTA11_78_2000001011 | Human | Colorectum | AD | 7.41e-14 | 3.59e-01 | -0.1088 |
50854 | SNHG32 | HTA11_347_2000001011 | Human | Colorectum | AD | 3.24e-26 | 5.40e-01 | -0.1954 |
50854 | SNHG32 | HTA11_411_2000001011 | Human | Colorectum | SER | 1.86e-06 | 5.38e-01 | -0.2602 |
50854 | SNHG32 | HTA11_3361_2000001011 | Human | Colorectum | AD | 9.32e-14 | 6.06e-01 | -0.1207 |
50854 | SNHG32 | HTA11_83_2000001011 | Human | Colorectum | SER | 4.95e-13 | 4.31e-01 | -0.1526 |
50854 | SNHG32 | HTA11_696_2000001011 | Human | Colorectum | AD | 1.23e-23 | 4.92e-01 | -0.1464 |
50854 | SNHG32 | HTA11_866_2000001011 | Human | Colorectum | AD | 3.84e-22 | 4.95e-01 | -0.1001 |
50854 | SNHG32 | HTA11_1391_2000001011 | Human | Colorectum | AD | 4.43e-37 | 8.88e-01 | -0.059 |
50854 | SNHG32 | HTA11_2992_2000001011 | Human | Colorectum | SER | 2.14e-07 | 3.56e-01 | -0.1706 |
50854 | SNHG32 | HTA11_5216_2000001011 | Human | Colorectum | SER | 2.49e-08 | 5.62e-01 | -0.1462 |
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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 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
Page: 1 |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
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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 |
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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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