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Gene: STOM |
Gene summary for STOM |
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Gene information | Species | Human | Gene symbol | STOM | Gene ID | 2040 |
Gene name | stomatin | |
Gene Alias | BND7 | |
Cytomap | 9q33.2 | |
Gene Type | protein-coding | GO ID | GO:0002028 | UniProtAcc | F8VSL7 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
2040 | STOM | LZE4T | Human | Esophagus | ESCC | 1.97e-14 | 7.94e-01 | 0.0811 |
2040 | STOM | LZE5T | Human | Esophagus | ESCC | 2.18e-04 | 1.82e-01 | 0.0514 |
2040 | STOM | LZE7T | Human | Esophagus | ESCC | 1.44e-07 | -1.96e-01 | 0.0667 |
2040 | STOM | LZE20T | Human | Esophagus | ESCC | 1.04e-09 | 8.52e-01 | 0.0662 |
2040 | STOM | LZE21D1 | Human | Esophagus | HGIN | 6.35e-04 | -2.51e-01 | 0.0632 |
2040 | STOM | LZE24D1 | Human | Esophagus | HGIN | 7.12e-08 | 3.34e-01 | 0.054 |
2040 | STOM | LZE24T | Human | Esophagus | ESCC | 2.51e-14 | 9.76e-01 | 0.0596 |
2040 | STOM | P2T-E | Human | Esophagus | ESCC | 1.46e-07 | 3.13e-01 | 0.1177 |
2040 | STOM | P4T-E | Human | Esophagus | ESCC | 9.71e-14 | 3.77e-01 | 0.1323 |
2040 | STOM | P5T-E | Human | Esophagus | ESCC | 1.40e-20 | 6.42e-01 | 0.1327 |
2040 | STOM | P9T-E | Human | Esophagus | ESCC | 9.62e-12 | 6.69e-01 | 0.1131 |
2040 | STOM | P10T-E | Human | Esophagus | ESCC | 2.46e-07 | -4.44e-01 | 0.116 |
2040 | STOM | P11T-E | Human | Esophagus | ESCC | 4.60e-06 | 6.64e-01 | 0.1426 |
2040 | STOM | P12T-E | Human | Esophagus | ESCC | 1.18e-47 | 1.55e+00 | 0.1122 |
2040 | STOM | P15T-E | Human | Esophagus | ESCC | 3.20e-37 | 1.26e+00 | 0.1149 |
2040 | STOM | P16T-E | Human | Esophagus | ESCC | 7.80e-16 | -2.68e-01 | 0.1153 |
2040 | STOM | P17T-E | Human | Esophagus | ESCC | 5.67e-03 | 6.19e-01 | 0.1278 |
2040 | STOM | P19T-E | Human | Esophagus | ESCC | 4.81e-03 | 1.23e+00 | 0.1662 |
2040 | STOM | P20T-E | Human | Esophagus | ESCC | 1.68e-16 | 7.22e-01 | 0.1124 |
2040 | STOM | P21T-E | Human | Esophagus | ESCC | 1.46e-28 | 1.06e+00 | 0.1617 |
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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:19012936 | Endometrium | EEC | nucleoside phosphate biosynthetic process | 43/2168 | 256/18723 | 7.79e-03 | 4.34e-02 | 43 |
GO:001603227 | Esophagus | HGIN | viral process | 118/2587 | 415/18723 | 3.01e-15 | 6.22e-13 | 118 |
GO:001905827 | Esophagus | HGIN | viral life cycle | 93/2587 | 317/18723 | 3.66e-13 | 5.63e-11 | 93 |
GO:001907926 | Esophagus | HGIN | viral genome replication | 48/2587 | 131/18723 | 4.65e-11 | 5.07e-09 | 48 |
GO:190382926 | Esophagus | HGIN | positive regulation of cellular protein localization | 75/2587 | 276/18723 | 3.19e-09 | 2.30e-07 | 75 |
GO:005079225 | Esophagus | HGIN | regulation of viral process | 50/2587 | 164/18723 | 2.53e-08 | 1.49e-06 | 50 |
GO:000660525 | Esophagus | HGIN | protein targeting | 78/2587 | 314/18723 | 1.08e-07 | 5.47e-06 | 78 |
GO:009015020 | Esophagus | HGIN | establishment of protein localization to membrane | 67/2587 | 260/18723 | 1.96e-07 | 9.57e-06 | 67 |
GO:004852419 | Esophagus | HGIN | positive regulation of viral process | 25/2587 | 65/18723 | 6.88e-07 | 2.95e-05 | 25 |
GO:004440326 | Esophagus | HGIN | biological process involved in symbiotic interaction | 71/2587 | 290/18723 | 7.09e-07 | 3.00e-05 | 71 |
GO:003238617 | Esophagus | HGIN | regulation of intracellular transport | 79/2587 | 337/18723 | 1.11e-06 | 4.36e-05 | 79 |
GO:003315720 | Esophagus | HGIN | regulation of intracellular protein transport | 58/2587 | 229/18723 | 2.29e-06 | 8.29e-05 | 58 |
GO:190495120 | Esophagus | HGIN | positive regulation of establishment of protein localization | 73/2587 | 319/18723 | 6.99e-06 | 2.14e-04 | 73 |
GO:003238820 | Esophagus | HGIN | positive regulation of intracellular transport | 51/2587 | 202/18723 | 1.00e-05 | 2.92e-04 | 51 |
GO:009031616 | Esophagus | HGIN | positive regulation of intracellular protein transport | 42/2587 | 160/18723 | 2.18e-05 | 5.78e-04 | 42 |
GO:005122220 | Esophagus | HGIN | positive regulation of protein transport | 67/2587 | 303/18723 | 5.13e-05 | 1.22e-03 | 67 |
GO:190547518 | Esophagus | HGIN | regulation of protein localization to membrane | 43/2587 | 175/18723 | 9.45e-05 | 2.03e-03 | 43 |
GO:00518518 | Esophagus | HGIN | modulation by host of symbiont process | 19/2587 | 60/18723 | 3.07e-04 | 5.15e-03 | 19 |
GO:00447888 | Esophagus | HGIN | modulation by host of viral process | 12/2587 | 30/18723 | 3.62e-04 | 5.68e-03 | 12 |
GO:00518177 | Esophagus | HGIN | modulation of process of other organism involved in symbiotic interaction | 23/2587 | 81/18723 | 4.52e-04 | 6.62e-03 | 23 |
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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 |
STOM | SNV | Missense_Mutation | c.863N>C | p.Gly288Ala | p.G288A | P27105 | protein_coding | tolerated(0.18) | benign(0) | TCGA-AN-A0FX-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
STOM | SNV | Missense_Mutation | novel | c.545N>T | p.Thr182Ile | p.T182I | P27105 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
STOM | SNV | Missense_Mutation | rs747153047 | c.295N>G | p.Ile99Val | p.I99V | P27105 | protein_coding | tolerated(1) | benign(0.001) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
STOM | SNV | Missense_Mutation | novel | c.428N>A | p.Thr143Asn | p.T143N | P27105 | protein_coding | deleterious(0) | probably_damaging(0.993) | TCGA-IR-A3L7-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
STOM | SNV | Missense_Mutation | c.431N>A | p.Arg144His | p.R144H | P27105 | protein_coding | tolerated(0.09) | benign(0.168) | TCGA-G4-6302-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
STOM | SNV | Missense_Mutation | rs763192503 | c.572N>A | p.Arg191His | p.R191H | P27105 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-NH-A50T-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
STOM | SNV | Missense_Mutation | rs201671242 | c.673N>A | p.Glu225Lys | p.E225K | P27105 | protein_coding | deleterious(0.02) | possibly_damaging(0.617) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
STOM | SNV | Missense_Mutation | rs867557202 | c.299N>T | p.Ser100Leu | p.S100L | P27105 | protein_coding | deleterious(0) | possibly_damaging(0.672) | TCGA-EI-6917-01 | Colorectum | rectum adenocarcinoma | Male | <65 | III/IV | Chemotherapy | 5fluorouracil+oxaciplatina+l-folinian | SD |
STOM | SNV | Missense_Mutation | novel | c.857N>G | p.His286Arg | p.H286R | P27105 | protein_coding | tolerated(0.17) | benign(0.003) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
STOM | SNV | Missense_Mutation | novel | c.752N>A | p.Arg251Gln | p.R251Q | P27105 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AJ-A3EL-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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