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Gene: NBPF12 |
Gene summary for NBPF12 |
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Gene information | Species | Human | Gene symbol | NBPF12 | Gene ID | 149013 |
Gene name | NBPF member 12 | |
Gene Alias | COAS1 | |
Cytomap | 1q21.1 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | A0A087WUF1 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
149013 | NBPF12 | HTA11_78_2000001011 | Human | Colorectum | AD | 3.33e-05 | 3.96e-01 | -0.1088 |
149013 | NBPF12 | HTA11_347_2000001011 | Human | Colorectum | AD | 4.29e-13 | 5.72e-01 | -0.1954 |
149013 | NBPF12 | HTA11_83_2000001011 | Human | Colorectum | SER | 2.29e-02 | 3.72e-01 | -0.1526 |
149013 | NBPF12 | HTA11_1391_2000001011 | Human | Colorectum | AD | 3.09e-02 | 3.62e-01 | -0.059 |
149013 | NBPF12 | HTA11_546_2000001011 | Human | Colorectum | AD | 5.62e-03 | 4.86e-01 | -0.0842 |
149013 | NBPF12 | HTA11_7663_2000001011 | Human | Colorectum | SER | 2.67e-02 | 5.03e-01 | 0.0131 |
149013 | NBPF12 | HTA11_10623_2000001011 | Human | Colorectum | AD | 2.22e-03 | 5.71e-01 | -0.0177 |
149013 | NBPF12 | HTA11_99999965062_69753 | Human | Colorectum | MSI-H | 2.35e-03 | 9.50e-01 | 0.3487 |
149013 | NBPF12 | F007 | Human | Colorectum | FAP | 2.02e-02 | -2.68e-01 | 0.1176 |
149013 | NBPF12 | A002-C-010 | Human | Colorectum | FAP | 3.71e-02 | -1.27e-01 | 0.242 |
149013 | NBPF12 | A015-C-203 | Human | Colorectum | FAP | 4.96e-13 | 4.16e-02 | -0.1294 |
149013 | NBPF12 | A001-C-108 | Human | Colorectum | FAP | 1.07e-06 | -5.29e-02 | -0.0272 |
149013 | NBPF12 | A002-C-205 | Human | Colorectum | FAP | 9.39e-04 | -5.95e-02 | -0.1236 |
149013 | NBPF12 | A015-C-006 | Human | Colorectum | FAP | 1.73e-03 | -1.87e-01 | -0.0994 |
149013 | NBPF12 | A015-C-106 | Human | Colorectum | FAP | 8.32e-05 | -1.47e-01 | -0.0511 |
149013 | NBPF12 | A002-C-114 | Human | Colorectum | FAP | 1.92e-04 | -1.26e-01 | -0.1561 |
149013 | NBPF12 | A015-C-104 | Human | Colorectum | FAP | 2.28e-11 | -1.52e-01 | -0.1899 |
149013 | NBPF12 | A001-C-014 | Human | Colorectum | FAP | 1.46e-02 | -1.00e-01 | 0.0135 |
149013 | NBPF12 | A002-C-016 | Human | Colorectum | FAP | 3.55e-06 | -1.27e-01 | 0.0521 |
149013 | NBPF12 | A001-C-203 | Human | Colorectum | FAP | 1.70e-02 | -2.79e-02 | -0.0481 |
Page: 1 2 3 4 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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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 |
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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 |
NBPF12 | SNV | Missense_Mutation | novel | c.1276N>A | p.Ala426Thr | p.A426T | protein_coding | deleterious(0.03) | probably_damaging(0.916) | TCGA-A5-A0GE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NBPF12 | SNV | Missense_Mutation | novel | c.2568N>G | p.Phe856Leu | p.F856L | protein_coding | tolerated(0.18) | benign(0.413) | TCGA-A5-A0GP-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NBPF12 | SNV | Missense_Mutation | novel | c.1259C>A | p.Ala420Asp | p.A420D | protein_coding | tolerated(0.05) | probably_damaging(0.959) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NBPF12 | SNV | Missense_Mutation | novel | c.2249C>T | p.Ala750Val | p.A750V | protein_coding | tolerated(0.41) | benign(0.413) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NBPF12 | SNV | Missense_Mutation | novel | c.917N>G | p.Phe306Cys | p.F306C | protein_coding | deleterious(0) | probably_damaging(0.977) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
NBPF12 | SNV | Missense_Mutation | novel | c.3467N>T | p.Ser1156Leu | p.S1156L | protein_coding | tolerated(1) | unknown(0) | TCGA-AJ-A5DW-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NBPF12 | SNV | Missense_Mutation | novel | c.1725G>T | p.Gln575His | p.Q575H | protein_coding | deleterious(0) | possibly_damaging(0.763) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
NBPF12 | SNV | Missense_Mutation | novel | c.2363A>G | p.His788Arg | p.H788R | protein_coding | deleterious(0.04) | benign(0.237) | TCGA-AP-A0LD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NBPF12 | SNV | Missense_Mutation | novel | c.2207N>T | p.Ala736Val | p.A736V | protein_coding | tolerated(0.28) | possibly_damaging(0.646) | TCGA-AP-A1DK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NBPF12 | SNV | Missense_Mutation | novel | c.2381N>T | p.Ala794Val | p.A794V | protein_coding | tolerated(0.17) | probably_damaging(0.979) | TCGA-AP-A1DK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 |
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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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