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Gene: IMPA1 |
Gene summary for IMPA1 |
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Gene information | Species | Human | Gene symbol | IMPA1 | Gene ID | 3612 |
Gene name | inositol monophosphatase 1 | |
Gene Alias | IMP | |
Cytomap | 8q21.13 | |
Gene Type | protein-coding | GO ID | GO:0005975 | UniProtAcc | A0A140VJL8 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
3612 | IMPA1 | LZE4T | Human | Esophagus | ESCC | 1.86e-08 | 2.20e-01 | 0.0811 |
3612 | IMPA1 | LZE8T | Human | Esophagus | ESCC | 1.93e-09 | 2.57e-01 | 0.067 |
3612 | IMPA1 | LZE20T | Human | Esophagus | ESCC | 3.99e-14 | 4.12e-01 | 0.0662 |
3612 | IMPA1 | LZE24T | Human | Esophagus | ESCC | 8.73e-15 | 2.79e-01 | 0.0596 |
3612 | IMPA1 | LZE6T | Human | Esophagus | ESCC | 7.92e-04 | 2.99e-01 | 0.0845 |
3612 | IMPA1 | P2T-E | Human | Esophagus | ESCC | 1.00e-16 | 2.10e-01 | 0.1177 |
3612 | IMPA1 | P4T-E | Human | Esophagus | ESCC | 6.95e-22 | 4.33e-01 | 0.1323 |
3612 | IMPA1 | P5T-E | Human | Esophagus | ESCC | 1.22e-14 | 3.09e-01 | 0.1327 |
3612 | IMPA1 | P8T-E | Human | Esophagus | ESCC | 4.21e-20 | 2.41e-01 | 0.0889 |
3612 | IMPA1 | P9T-E | Human | Esophagus | ESCC | 4.94e-11 | 2.08e-01 | 0.1131 |
3612 | IMPA1 | P10T-E | Human | Esophagus | ESCC | 1.43e-21 | 1.70e-01 | 0.116 |
3612 | IMPA1 | P11T-E | Human | Esophagus | ESCC | 6.50e-13 | 3.96e-01 | 0.1426 |
3612 | IMPA1 | P12T-E | Human | Esophagus | ESCC | 1.30e-12 | 2.83e-01 | 0.1122 |
3612 | IMPA1 | P15T-E | Human | Esophagus | ESCC | 1.08e-17 | 3.31e-01 | 0.1149 |
3612 | IMPA1 | P16T-E | Human | Esophagus | ESCC | 4.33e-18 | 4.32e-01 | 0.1153 |
3612 | IMPA1 | P17T-E | Human | Esophagus | ESCC | 8.17e-04 | 2.74e-01 | 0.1278 |
3612 | IMPA1 | P19T-E | Human | Esophagus | ESCC | 2.31e-09 | 5.28e-01 | 0.1662 |
3612 | IMPA1 | P20T-E | Human | Esophagus | ESCC | 4.35e-16 | 3.78e-01 | 0.1124 |
3612 | IMPA1 | P21T-E | Human | Esophagus | ESCC | 7.09e-14 | 2.47e-01 | 0.1617 |
3612 | IMPA1 | P22T-E | Human | Esophagus | ESCC | 4.10e-10 | 1.12e-01 | 0.1236 |
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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 |
Liver | Cyst | ![]() |
Lung | IAC | ![]() |
Lung | AIS | ![]() |
Lung | AAH | ![]() |
Lung | MIAC | ![]() |
∗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:001631110 | Esophagus | ESCC | dephosphorylation | 251/8552 | 417/18723 | 1.26e-09 | 2.99e-08 | 251 |
GO:00086544 | Esophagus | ESCC | phospholipid biosynthetic process | 162/8552 | 253/18723 | 2.59e-09 | 5.73e-08 | 162 |
GO:00464744 | Esophagus | ESCC | glycerophospholipid biosynthetic process | 135/8552 | 211/18723 | 5.75e-08 | 1.02e-06 | 135 |
GO:00450175 | Esophagus | ESCC | glycerolipid biosynthetic process | 154/8552 | 252/18723 | 5.20e-07 | 6.96e-06 | 154 |
GO:00066446 | Esophagus | ESCC | phospholipid metabolic process | 218/8552 | 383/18723 | 5.37e-06 | 5.59e-05 | 218 |
GO:00060668 | Esophagus | ESCC | alcohol metabolic process | 202/8552 | 353/18723 | 7.32e-06 | 7.26e-05 | 202 |
GO:00066505 | Esophagus | ESCC | glycerophospholipid metabolic process | 174/8552 | 306/18723 | 4.92e-05 | 3.85e-04 | 174 |
GO:00442626 | Esophagus | ESCC | cellular carbohydrate metabolic process | 160/8552 | 283/18723 | 1.43e-04 | 9.66e-04 | 160 |
GO:00160514 | Esophagus | ESCC | carbohydrate biosynthetic process | 117/8552 | 202/18723 | 2.96e-04 | 1.79e-03 | 117 |
GO:00464864 | Esophagus | ESCC | glycerolipid metabolic process | 211/8552 | 392/18723 | 6.51e-04 | 3.46e-03 | 211 |
GO:00461653 | Esophagus | ESCC | alcohol biosynthetic process | 83/8552 | 140/18723 | 8.04e-04 | 4.16e-03 | 83 |
GO:00442827 | Esophagus | ESCC | small molecule catabolic process | 201/8552 | 376/18723 | 1.35e-03 | 6.41e-03 | 201 |
GO:19016174 | Esophagus | ESCC | organic hydroxy compound biosynthetic process | 128/8552 | 237/18723 | 5.86e-03 | 2.16e-02 | 128 |
GO:00346372 | Esophagus | ESCC | cellular carbohydrate biosynthetic process | 46/8552 | 78/18723 | 1.24e-02 | 4.13e-02 | 46 |
GO:00066611 | Esophagus | ESCC | phosphatidylinositol biosynthetic process | 73/8552 | 131/18723 | 1.31e-02 | 4.28e-02 | 73 |
GO:00442825 | Liver | NAFLD | small molecule catabolic process | 91/1882 | 376/18723 | 8.96e-16 | 1.31e-12 | 91 |
GO:00442623 | Liver | NAFLD | cellular carbohydrate metabolic process | 55/1882 | 283/18723 | 1.27e-06 | 6.01e-05 | 55 |
GO:0016051 | Liver | NAFLD | carbohydrate biosynthetic process | 43/1882 | 202/18723 | 1.55e-06 | 6.96e-05 | 43 |
GO:00060666 | Liver | NAFLD | alcohol metabolic process | 62/1882 | 353/18723 | 9.01e-06 | 2.96e-04 | 62 |
GO:00464863 | Liver | NAFLD | glycerolipid metabolic process | 66/1882 | 392/18723 | 1.94e-05 | 5.52e-04 | 66 |
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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 |
IMPA1 | SNV | Missense_Mutation | c.122N>C | p.Ser41Thr | p.S41T | P29218 | protein_coding | tolerated_low_confidence(0.42) | benign(0.001) | TCGA-A7-A0DA-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | |
IMPA1 | SNV | Missense_Mutation | c.116N>C | p.Gly39Ala | p.G39A | P29218 | protein_coding | deleterious_low_confidence(0.04) | benign(0.081) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
IMPA1 | deletion | Frame_Shift_Del | c.970delG | p.Glu324LysfsTer15 | p.E324Kfs*15 | P29218 | protein_coding | TCGA-A7-A4SA-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | CR | |||
IMPA1 | deletion | In_Frame_Del | novel | c.746_748delNNN | p.Ile249del | p.I249del | P29218 | protein_coding | TCGA-AN-A0FN-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
IMPA1 | SNV | Missense_Mutation | novel | c.788C>G | p.Ala263Gly | p.A263G | P29218 | protein_coding | deleterious(0) | probably_damaging(0.914) | TCGA-EA-A97N-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
IMPA1 | SNV | Missense_Mutation | c.959N>T | p.Arg320Met | p.R320M | P29218 | protein_coding | tolerated(0.06) | benign(0.061) | TCGA-A6-3809-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
IMPA1 | SNV | Missense_Mutation | c.703N>A | p.Leu235Ile | p.L235I | P29218 | protein_coding | tolerated(0.13) | benign(0.184) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
IMPA1 | SNV | Missense_Mutation | novel | c.689N>A | p.Thr230Asn | p.T230N | P29218 | protein_coding | tolerated(0.16) | benign(0.011) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
IMPA1 | SNV | Missense_Mutation | novel | c.259N>C | p.Lys87Gln | p.K87Q | P29218 | protein_coding | tolerated(0.34) | benign(0.001) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
IMPA1 | SNV | Missense_Mutation | rs767783535 | c.1000G>A | p.Asp334Asn | p.D334N | P29218 | protein_coding | deleterious(0) | probably_damaging(0.946) | TCGA-A5-A0GP-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 |
3612 | IMPA1 | ENZYME, DRUGGABLE GENOME | inhibitor | CHEMBL2103738 | LITHIUM CITRATE | |
3612 | IMPA1 | ENZYME, DRUGGABLE GENOME | inhibitor | 178101897 | ||
3612 | IMPA1 | ENZYME, DRUGGABLE GENOME | inhibitor | CHEMBL1200826 | LITHIUM CARBONATE |
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