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Gene: BPNT1 |
Gene summary for BPNT1 |
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Gene information | Species | Human | Gene symbol | BPNT1 | Gene ID | 10380 |
Gene name | 3'(2'), 5'-bisphosphate nucleotidase 1 | |
Gene Alias | HEL20 | |
Cytomap | 1q41 | |
Gene Type | protein-coding | GO ID | GO:0005975 | UniProtAcc | O95861 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
10380 | BPNT1 | HTA11_2487_2000001011 | Human | Colorectum | SER | 8.96e-08 | 4.84e-01 | -0.1808 |
10380 | BPNT1 | HTA11_1938_2000001011 | Human | Colorectum | AD | 1.97e-06 | 3.82e-01 | -0.0811 |
10380 | BPNT1 | HTA11_347_2000001011 | Human | Colorectum | AD | 1.22e-12 | 4.20e-01 | -0.1954 |
10380 | BPNT1 | HTA11_696_2000001011 | Human | Colorectum | AD | 2.70e-04 | 2.54e-01 | -0.1464 |
10380 | BPNT1 | LZE4T | Human | Esophagus | ESCC | 1.10e-02 | 5.53e-02 | 0.0811 |
10380 | BPNT1 | LZE7T | Human | Esophagus | ESCC | 2.01e-07 | 3.12e-01 | 0.0667 |
10380 | BPNT1 | LZE20T | Human | Esophagus | ESCC | 2.98e-03 | 1.64e-01 | 0.0662 |
10380 | BPNT1 | LZE22T | Human | Esophagus | ESCC | 4.61e-04 | 2.81e-01 | 0.068 |
10380 | BPNT1 | LZE24T | Human | Esophagus | ESCC | 9.91e-08 | 2.11e-01 | 0.0596 |
10380 | BPNT1 | P1T-E | Human | Esophagus | ESCC | 7.43e-03 | 2.23e-01 | 0.0875 |
10380 | BPNT1 | P2T-E | Human | Esophagus | ESCC | 3.93e-18 | 2.18e-01 | 0.1177 |
10380 | BPNT1 | P4T-E | Human | Esophagus | ESCC | 2.69e-13 | 1.87e-01 | 0.1323 |
10380 | BPNT1 | P5T-E | Human | Esophagus | ESCC | 5.06e-07 | 1.61e-01 | 0.1327 |
10380 | BPNT1 | P8T-E | Human | Esophagus | ESCC | 3.79e-18 | 2.08e-01 | 0.0889 |
10380 | BPNT1 | P9T-E | Human | Esophagus | ESCC | 2.43e-04 | 6.01e-02 | 0.1131 |
10380 | BPNT1 | P10T-E | Human | Esophagus | ESCC | 1.09e-11 | 1.71e-01 | 0.116 |
10380 | BPNT1 | P11T-E | Human | Esophagus | ESCC | 1.37e-10 | 2.67e-01 | 0.1426 |
10380 | BPNT1 | P12T-E | Human | Esophagus | ESCC | 3.55e-06 | 1.52e-01 | 0.1122 |
10380 | BPNT1 | P15T-E | Human | Esophagus | ESCC | 4.02e-15 | 2.35e-01 | 0.1149 |
10380 | BPNT1 | P16T-E | Human | Esophagus | ESCC | 4.67e-10 | 2.00e-01 | 0.1153 |
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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:00464743 | Oral cavity | OSCC | glycerophospholipid biosynthetic process | 102/7305 | 211/18723 | 3.50e-03 | 1.48e-02 | 102 |
GO:00066445 | Oral cavity | OSCC | phospholipid metabolic process | 175/7305 | 383/18723 | 4.21e-03 | 1.71e-02 | 175 |
GO:00442625 | Oral cavity | OSCC | cellular carbohydrate metabolic process | 130/7305 | 283/18723 | 9.98e-03 | 3.49e-02 | 130 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa00920 | Colorectum | AD | Sulfur metabolism | 8/2092 | 10/8465 | 3.78e-04 | 2.82e-03 | 1.80e-03 | 8 |
hsa009201 | Colorectum | AD | Sulfur metabolism | 8/2092 | 10/8465 | 3.78e-04 | 2.82e-03 | 1.80e-03 | 8 |
hsa0092010 | Esophagus | ESCC | Sulfur metabolism | 9/4205 | 10/8465 | 1.01e-02 | 2.38e-02 | 1.22e-02 | 9 |
hsa0092011 | Esophagus | ESCC | Sulfur metabolism | 9/4205 | 10/8465 | 1.01e-02 | 2.38e-02 | 1.22e-02 | 9 |
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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 |
BPNT1 | SNV | Missense_Mutation | c.352N>T | p.Pro118Ser | p.P118S | O95861 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A8-A06Q-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
BPNT1 | SNV | Missense_Mutation | novel | c.689N>G | p.Glu230Gly | p.E230G | O95861 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-AC-A2QI-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | cytoxan | CR |
BPNT1 | SNV | Missense_Mutation | novel | c.732N>C | p.Lys244Asn | p.K244N | O95861 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-MY-A5BF-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | CR |
BPNT1 | SNV | Missense_Mutation | rs760682156 | c.790N>A | p.Asp264Asn | p.D264N | O95861 | protein_coding | tolerated(0.07) | probably_damaging(0.977) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
BPNT1 | SNV | Missense_Mutation | rs776487679 | c.155N>A | p.Arg52Gln | p.R52Q | O95861 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-AY-6197-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
BPNT1 | SNV | Missense_Mutation | rs776487679 | c.155N>A | p.Arg52Gln | p.R52Q | O95861 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
BPNT1 | SNV | Missense_Mutation | novel | c.56C>T | p.Ala19Val | p.A19V | O95861 | protein_coding | deleterious(0.04) | possibly_damaging(0.818) | TCGA-CK-5913-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
BPNT1 | SNV | Missense_Mutation | c.82N>T | p.Arg28Cys | p.R28C | O95861 | protein_coding | deleterious(0.01) | benign(0.001) | TCGA-G4-6588-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
BPNT1 | SNV | Missense_Mutation | novel | c.372N>C | p.Glu124Asp | p.E124D | O95861 | protein_coding | deleterious(0.03) | possibly_damaging(0.773) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
BPNT1 | SNV | Missense_Mutation | c.82C>T | p.Arg28Cys | p.R28C | O95861 | protein_coding | deleterious(0.01) | benign(0.001) | TCGA-AP-A051-01 | 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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