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Gene: TMEM189 |
Gene summary for TMEM189 |
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Gene information | Species | Human | Gene symbol | TMEM189 | Gene ID | 387521 |
Gene name | plasmanylethanolamine desaturase 1 | |
Gene Alias | CarF | |
Cytomap | 20q13.13 | |
Gene Type | protein-coding | GO ID | GO:0006082 | UniProtAcc | A5PLL7 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
387521 | TMEM189 | P19T-E | Human | Esophagus | ESCC | 1.37e-06 | 7.30e-01 | 0.1662 |
387521 | TMEM189 | P20T-E | Human | Esophagus | ESCC | 3.78e-52 | 1.23e+00 | 0.1124 |
387521 | TMEM189 | P21T-E | Human | Esophagus | ESCC | 3.38e-87 | 1.79e+00 | 0.1617 |
387521 | TMEM189 | P22T-E | Human | Esophagus | ESCC | 4.13e-57 | 9.49e-01 | 0.1236 |
387521 | TMEM189 | P23T-E | Human | Esophagus | ESCC | 4.97e-57 | 1.57e+00 | 0.108 |
387521 | TMEM189 | P24T-E | Human | Esophagus | ESCC | 1.11e-50 | 1.05e+00 | 0.1287 |
387521 | TMEM189 | P26T-E | Human | Esophagus | ESCC | 2.75e-105 | 1.84e+00 | 0.1276 |
387521 | TMEM189 | P27T-E | Human | Esophagus | ESCC | 1.92e-35 | 6.11e-01 | 0.1055 |
387521 | TMEM189 | P28T-E | Human | Esophagus | ESCC | 6.87e-51 | 1.01e+00 | 0.1149 |
387521 | TMEM189 | P30T-E | Human | Esophagus | ESCC | 4.22e-58 | 1.73e+00 | 0.137 |
387521 | TMEM189 | P31T-E | Human | Esophagus | ESCC | 1.30e-84 | 1.29e+00 | 0.1251 |
387521 | TMEM189 | P32T-E | Human | Esophagus | ESCC | 1.08e-87 | 1.69e+00 | 0.1666 |
387521 | TMEM189 | P36T-E | Human | Esophagus | ESCC | 2.21e-33 | 1.12e+00 | 0.1187 |
387521 | TMEM189 | P37T-E | Human | Esophagus | ESCC | 3.36e-33 | 9.97e-01 | 0.1371 |
387521 | TMEM189 | P38T-E | Human | Esophagus | ESCC | 3.79e-13 | 6.53e-01 | 0.127 |
387521 | TMEM189 | P39T-E | Human | Esophagus | ESCC | 4.22e-44 | 7.36e-01 | 0.0894 |
387521 | TMEM189 | P40T-E | Human | Esophagus | ESCC | 3.21e-18 | 6.10e-01 | 0.109 |
387521 | TMEM189 | P42T-E | Human | Esophagus | ESCC | 1.69e-38 | 1.23e+00 | 0.1175 |
387521 | TMEM189 | P44T-E | Human | Esophagus | ESCC | 2.34e-22 | 8.39e-01 | 0.1096 |
387521 | TMEM189 | P47T-E | Human | Esophagus | ESCC | 5.36e-49 | 1.12e+00 | 0.1067 |
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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 |
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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 |
TMEM189 | SNV | Missense_Mutation | rs201575410 | c.761N>T | p.Thr254Met | p.T254M | A5PLL7 | protein_coding | deleterious(0) | probably_damaging(0.992) | TCGA-EA-A3HS-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
TMEM189 | SNV | Missense_Mutation | novel | c.786N>G | p.Asp262Glu | p.D262E | A5PLL7 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AG-A01N-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | capecitabine | SD |
TMEM189 | insertion | Frame_Shift_Ins | novel | c.776_777insAATTT | p.Ala260IlefsTer6 | p.A260Ifs*6 | A5PLL7 | protein_coding | TCGA-AM-5820-01 | Colorectum | colon adenocarcinoma | 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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