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Gene: TMEM25 |
Gene summary for TMEM25 |
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Gene information | Species | Human | Gene symbol | TMEM25 | Gene ID | 84866 |
Gene name | transmembrane protein 25 | |
Gene Alias | TMEM25 | |
Cytomap | 11q23.3 | |
Gene Type | protein-coding | GO ID | GO:0003008 | UniProtAcc | Q86YD3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
84866 | TMEM25 | LZE4T | Human | Esophagus | ESCC | 2.32e-04 | 1.37e-01 | 0.0811 |
84866 | TMEM25 | LZE22T | Human | Esophagus | ESCC | 2.36e-07 | 6.38e-01 | 0.068 |
84866 | TMEM25 | LZE24T | Human | Esophagus | ESCC | 2.44e-11 | 3.13e-01 | 0.0596 |
84866 | TMEM25 | P2T-E | Human | Esophagus | ESCC | 7.77e-17 | 2.35e-01 | 0.1177 |
84866 | TMEM25 | P4T-E | Human | Esophagus | ESCC | 9.35e-18 | 4.19e-01 | 0.1323 |
84866 | TMEM25 | P5T-E | Human | Esophagus | ESCC | 4.68e-11 | 1.77e-01 | 0.1327 |
84866 | TMEM25 | P8T-E | Human | Esophagus | ESCC | 1.55e-10 | 2.36e-01 | 0.0889 |
84866 | TMEM25 | P9T-E | Human | Esophagus | ESCC | 1.27e-07 | 1.27e-01 | 0.1131 |
84866 | TMEM25 | P10T-E | Human | Esophagus | ESCC | 2.46e-17 | 3.60e-01 | 0.116 |
84866 | TMEM25 | P11T-E | Human | Esophagus | ESCC | 1.87e-15 | 6.49e-01 | 0.1426 |
84866 | TMEM25 | P12T-E | Human | Esophagus | ESCC | 5.62e-30 | 4.52e-01 | 0.1122 |
84866 | TMEM25 | P15T-E | Human | Esophagus | ESCC | 3.44e-04 | 1.22e-01 | 0.1149 |
84866 | TMEM25 | P16T-E | Human | Esophagus | ESCC | 3.65e-28 | 5.04e-01 | 0.1153 |
84866 | TMEM25 | P17T-E | Human | Esophagus | ESCC | 1.47e-03 | 2.64e-01 | 0.1278 |
84866 | TMEM25 | P21T-E | Human | Esophagus | ESCC | 1.47e-34 | 6.55e-01 | 0.1617 |
84866 | TMEM25 | P22T-E | Human | Esophagus | ESCC | 1.14e-14 | 2.86e-01 | 0.1236 |
84866 | TMEM25 | P24T-E | Human | Esophagus | ESCC | 2.17e-08 | 1.43e-01 | 0.1287 |
84866 | TMEM25 | P26T-E | Human | Esophagus | ESCC | 8.63e-21 | 4.25e-01 | 0.1276 |
84866 | TMEM25 | P27T-E | Human | Esophagus | ESCC | 1.78e-17 | 2.56e-01 | 0.1055 |
84866 | TMEM25 | P28T-E | Human | Esophagus | ESCC | 1.49e-10 | 1.16e-01 | 0.1149 |
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Tissue | Expression Dynamics | Abbreviation |
Esophagus | ![]() | ESCC: Esophageal squamous cell carcinoma |
HGIN: High-grade intraepithelial neoplasias | ||
LGIN: Low-grade intraepithelial neoplasias |
∗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:1905897112 | Skin | cSCC | regulation of response to endoplasmic reticulum stress | 47/4864 | 82/18723 | 1.78e-09 | 6.62e-08 | 47 |
GO:190589814 | Skin | cSCC | positive regulation of response to endoplasmic reticulum stress | 24/4864 | 35/18723 | 1.56e-07 | 3.51e-06 | 24 |
GO:00365037 | Skin | cSCC | ERAD pathway | 51/4864 | 107/18723 | 1.11e-06 | 1.95e-05 | 51 |
GO:007099729 | Skin | cSCC | neuron death | 133/4864 | 361/18723 | 2.91e-06 | 4.58e-05 | 133 |
GO:00064877 | Skin | cSCC | protein N-linked glycosylation | 33/4864 | 65/18723 | 1.63e-05 | 1.99e-04 | 33 |
GO:190121426 | Skin | cSCC | regulation of neuron death | 112/4864 | 319/18723 | 1.71e-04 | 1.48e-03 | 112 |
GO:19042944 | Skin | cSCC | positive regulation of ERAD pathway | 10/4864 | 14/18723 | 4.77e-04 | 3.60e-03 | 10 |
GO:19042923 | Skin | cSCC | regulation of ERAD pathway | 12/4864 | 20/18723 | 1.34e-03 | 8.54e-03 | 12 |
GO:0010498113 | Thyroid | PTC | proteasomal protein catabolic process | 297/5968 | 490/18723 | 4.58e-40 | 9.63e-37 | 297 |
GO:0009896113 | Thyroid | PTC | positive regulation of catabolic process | 278/5968 | 492/18723 | 3.35e-30 | 2.64e-27 | 278 |
GO:0031331113 | Thyroid | PTC | positive regulation of cellular catabolic process | 249/5968 | 427/18723 | 5.28e-30 | 3.58e-27 | 249 |
GO:0042176113 | Thyroid | PTC | regulation of protein catabolic process | 231/5968 | 391/18723 | 4.76e-29 | 2.14e-26 | 231 |
GO:1903362113 | Thyroid | PTC | regulation of cellular protein catabolic process | 162/5968 | 255/18723 | 1.62e-25 | 5.12e-23 | 162 |
GO:0034976113 | Thyroid | PTC | response to endoplasmic reticulum stress | 161/5968 | 256/18723 | 1.14e-24 | 3.27e-22 | 161 |
GO:1903050113 | Thyroid | PTC | regulation of proteolysis involved in cellular protein catabolic process | 140/5968 | 221/18723 | 4.63e-22 | 1.01e-19 | 140 |
GO:0045732113 | Thyroid | PTC | positive regulation of protein catabolic process | 142/5968 | 231/18723 | 1.43e-20 | 2.38e-18 | 142 |
GO:0061136113 | Thyroid | PTC | regulation of proteasomal protein catabolic process | 121/5968 | 187/18723 | 2.25e-20 | 3.37e-18 | 121 |
GO:1903364113 | Thyroid | PTC | positive regulation of cellular protein catabolic process | 104/5968 | 155/18723 | 1.93e-19 | 2.39e-17 | 104 |
GO:0045862113 | Thyroid | PTC | positive regulation of proteolysis | 198/5968 | 372/18723 | 6.68e-18 | 6.91e-16 | 198 |
GO:1901800112 | Thyroid | PTC | positive regulation of proteasomal protein catabolic process | 80/5968 | 114/18723 | 4.80e-17 | 4.27e-15 | 80 |
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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 |
TMEM25 | deletion | Frame_Shift_Del | novel | c.575delA | p.Asn192ThrfsTer85 | p.N192Tfs*85 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD | |||
TMEM25 | SNV | Missense_Mutation | novel | c.758G>A | p.Ser253Asn | p.S253N | protein_coding | tolerated(0.29) | benign(0.062) | TCGA-C5-A8XK-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | SD | |
TMEM25 | SNV | Missense_Mutation | rs782188288 | c.145G>A | p.Ala49Thr | p.A49T | protein_coding | tolerated(0.54) | benign(0.207) | TCGA-EA-A410-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
TMEM25 | SNV | Missense_Mutation | c.1033N>T | p.Leu345Phe | p.L345F | protein_coding | tolerated_low_confidence(0.07) | benign(0.015) | TCGA-FU-A3EO-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | ||
TMEM25 | SNV | Missense_Mutation | novel | c.97N>A | p.Asp33Asn | p.D33N | protein_coding | tolerated(0.2) | probably_damaging(0.998) | TCGA-IR-A3LK-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | PD | |
TMEM25 | SNV | Missense_Mutation | novel | c.224G>A | p.Ser75Asn | p.S75N | protein_coding | tolerated(0.51) | benign(0.007) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
TMEM25 | SNV | Missense_Mutation | rs377765778 | c.599N>A | p.Arg200His | p.R200H | protein_coding | tolerated(0.3) | benign(0.003) | TCGA-AZ-6598-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
TMEM25 | SNV | Missense_Mutation | rs75184401 | c.458C>T | p.Ala153Val | p.A153V | protein_coding | tolerated(0.5) | benign(0.213) | TCGA-AG-3883-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
TMEM25 | deletion | Frame_Shift_Del | c.166delN | p.Pro58LeufsTer23 | p.P58Lfs*23 | protein_coding | TCGA-5M-AAT6-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | PD | ||||
TMEM25 | deletion | Frame_Shift_Del | c.166delN | p.Pro58LeufsTer23 | p.P58Lfs*23 | protein_coding | TCGA-A6-3809-01 | 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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