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Gene: PPP1R9B |
Gene summary for PPP1R9B |
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Gene information | Species | Human | Gene symbol | PPP1R9B | Gene ID | 84687 |
Gene name | protein phosphatase 1 regulatory subunit 9B | |
Gene Alias | PPP1R6 | |
Cytomap | 17q21.33 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | D3DTX6 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
84687 | PPP1R9B | HCC1_Meng | Human | Liver | HCC | 2.31e-24 | 2.71e-02 | 0.0246 |
84687 | PPP1R9B | HCC2_Meng | Human | Liver | HCC | 4.01e-10 | 9.40e-02 | 0.0107 |
84687 | PPP1R9B | HCC2 | Human | Liver | HCC | 1.23e-06 | 1.26e+00 | 0.5341 |
84687 | PPP1R9B | S014 | Human | Liver | HCC | 4.72e-09 | 3.55e-01 | 0.2254 |
84687 | PPP1R9B | S015 | Human | Liver | HCC | 8.41e-13 | 5.14e-01 | 0.2375 |
84687 | PPP1R9B | S016 | Human | Liver | HCC | 1.43e-13 | 4.04e-01 | 0.2243 |
84687 | PPP1R9B | S027 | Human | Liver | HCC | 2.66e-06 | 4.72e-01 | 0.2446 |
84687 | PPP1R9B | S028 | Human | Liver | HCC | 3.75e-19 | 5.64e-01 | 0.2503 |
84687 | PPP1R9B | S029 | Human | Liver | HCC | 5.55e-15 | 5.42e-01 | 0.2581 |
84687 | PPP1R9B | C04 | Human | Oral cavity | OSCC | 1.27e-11 | 4.83e-01 | 0.2633 |
84687 | PPP1R9B | C21 | Human | Oral cavity | OSCC | 3.67e-02 | 1.57e-01 | 0.2678 |
84687 | PPP1R9B | C30 | Human | Oral cavity | OSCC | 3.71e-29 | 1.09e+00 | 0.3055 |
84687 | PPP1R9B | C38 | Human | Oral cavity | OSCC | 6.91e-04 | 5.55e-01 | 0.172 |
84687 | PPP1R9B | C43 | Human | Oral cavity | OSCC | 8.03e-03 | 1.28e-01 | 0.1704 |
84687 | PPP1R9B | C46 | Human | Oral cavity | OSCC | 6.35e-05 | 1.28e-01 | 0.1673 |
84687 | PPP1R9B | C51 | Human | Oral cavity | OSCC | 1.98e-10 | 4.70e-01 | 0.2674 |
84687 | PPP1R9B | C08 | Human | Oral cavity | OSCC | 1.55e-02 | 1.37e-01 | 0.1919 |
84687 | PPP1R9B | SYSMH1 | Human | Oral cavity | OSCC | 2.09e-03 | 1.64e-01 | 0.1127 |
84687 | PPP1R9B | SYSMH3 | Human | Oral cavity | OSCC | 1.90e-12 | 4.00e-01 | 0.2442 |
84687 | PPP1R9B | SYSMH5 | Human | Oral cavity | OSCC | 9.86e-03 | 1.78e-01 | 0.0647 |
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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:0072659112 | Thyroid | PTC | protein localization to plasma membrane | 153/5968 | 284/18723 | 9.90e-15 | 6.50e-13 | 153 |
GO:1990778111 | Thyroid | PTC | protein localization to cell periphery | 172/5968 | 333/18723 | 3.71e-14 | 2.30e-12 | 172 |
GO:0016049112 | Thyroid | PTC | cell growth | 225/5968 | 482/18723 | 4.75e-12 | 2.07e-10 | 225 |
GO:000815426 | Thyroid | PTC | actin polymerization or depolymerization | 117/5968 | 218/18723 | 1.85e-11 | 7.21e-10 | 117 |
GO:000734619 | Thyroid | PTC | regulation of mitotic cell cycle | 212/5968 | 457/18723 | 4.03e-11 | 1.44e-09 | 212 |
GO:0071496113 | Thyroid | PTC | cellular response to external stimulus | 158/5968 | 320/18723 | 4.12e-11 | 1.47e-09 | 158 |
GO:004477218 | Thyroid | PTC | mitotic cell cycle phase transition | 196/5968 | 424/18723 | 3.17e-10 | 1.02e-08 | 196 |
GO:1901653111 | Thyroid | PTC | cellular response to peptide | 169/5968 | 359/18723 | 9.81e-10 | 2.89e-08 | 169 |
GO:0032984110 | Thyroid | PTC | protein-containing complex disassembly | 114/5968 | 224/18723 | 2.26e-09 | 6.33e-08 | 114 |
GO:0001558111 | Thyroid | PTC | regulation of cell growth | 188/5968 | 414/18723 | 4.13e-09 | 1.09e-07 | 188 |
GO:0048545113 | Thyroid | PTC | response to steroid hormone | 158/5968 | 339/18723 | 8.10e-09 | 2.00e-07 | 158 |
GO:1904375111 | Thyroid | PTC | regulation of protein localization to cell periphery | 70/5968 | 125/18723 | 2.04e-08 | 4.71e-07 | 70 |
GO:0031668113 | Thyroid | PTC | cellular response to extracellular stimulus | 120/5968 | 246/18723 | 2.13e-08 | 4.91e-07 | 120 |
GO:190547525 | Thyroid | PTC | regulation of protein localization to membrane | 91/5968 | 175/18723 | 2.41e-08 | 5.43e-07 | 91 |
GO:01400148 | Thyroid | PTC | mitotic nuclear division | 135/5968 | 287/18723 | 4.90e-08 | 1.04e-06 | 135 |
GO:19019908 | Thyroid | PTC | regulation of mitotic cell cycle phase transition | 138/5968 | 299/18723 | 1.44e-07 | 2.78e-06 | 138 |
GO:0007568111 | Thyroid | PTC | aging | 153/5968 | 339/18723 | 1.80e-07 | 3.34e-06 | 153 |
GO:001635819 | Thyroid | PTC | dendrite development | 115/5968 | 243/18723 | 3.16e-07 | 5.35e-06 | 115 |
GO:1903076112 | Thyroid | PTC | regulation of protein localization to plasma membrane | 58/5968 | 104/18723 | 3.91e-07 | 6.51e-06 | 58 |
GO:003530427 | Thyroid | PTC | regulation of protein dephosphorylation | 51/5968 | 90/18723 | 1.01e-06 | 1.50e-05 | 51 |
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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 |
PPP1R9B | SNV | Missense_Mutation | novel | c.1697N>T | p.Ala566Val | p.A566V | protein_coding | deleterious(0.04) | probably_damaging(0.998) | TCGA-AO-A128-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD | |
PPP1R9B | deletion | Frame_Shift_Del | novel | c.1136delT | p.Val379GlufsTer17 | p.V379Efs*17 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD | |||
PPP1R9B | SNV | Missense_Mutation | novel | c.144G>C | p.Lys48Asn | p.K48N | protein_coding | deleterious(0) | benign(0.362) | TCGA-EK-A3GK-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
PPP1R9B | SNV | Missense_Mutation | novel | c.1526N>A | p.Ser509Asn | p.S509N | protein_coding | deleterious(0) | possibly_damaging(0.726) | TCGA-GH-A9DA-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
PPP1R9B | SNV | Missense_Mutation | novel | c.1439C>G | p.Ser480Cys | p.S480C | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-IR-A3LK-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | PD | |
PPP1R9B | SNV | Missense_Mutation | novel | c.1552N>C | p.Asp518His | p.D518H | protein_coding | deleterious(0) | probably_damaging(0.955) | TCGA-Q1-A73O-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
PPP1R9B | SNV | Missense_Mutation | novel | c.1282N>C | p.Glu428Gln | p.E428Q | protein_coding | deleterious(0.03) | possibly_damaging(0.543) | TCGA-VS-A9UI-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
PPP1R9B | insertion | Frame_Shift_Ins | novel | c.1096_1097insG | p.Val366GlyfsTer12 | p.V366Gfs*12 | protein_coding | TCGA-VS-A94Z-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |||
PPP1R9B | SNV | Missense_Mutation | novel | c.2221N>A | p.Leu741Met | p.L741M | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AA-3950-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
PPP1R9B | SNV | Missense_Mutation | novel | c.1930G>T | p.Ala644Ser | p.A644S | protein_coding | tolerated(0.34) | benign(0.057) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | 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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