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Gene: TMEM132D |
Gene summary for TMEM132D |
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Gene information | Species | Human | Gene symbol | TMEM132D | Gene ID | 121256 |
Gene name | transmembrane protein 132D | |
Gene Alias | MOLT | |
Cytomap | 12q24.33 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | Q14C87 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
121256 | TMEM132D | RNA-P23T2-P23T2-4 | Human | Lung | MIAC | 4.84e-05 | 1.34e+00 | -0.0272 |
121256 | TMEM132D | RNA-P24T2-P24T2-2 | Human | Lung | IAC | 4.72e-06 | 1.42e+00 | 0.0057 |
121256 | TMEM132D | RNA-P5T2-P5T2-1 | Human | Lung | MIAC | 2.56e-04 | 1.44e+00 | -0.0135 |
121256 | TMEM132D | RNA-P6T1-P6T1-1 | Human | Lung | MIAC | 6.72e-03 | 9.50e-01 | -0.0238 |
121256 | TMEM132D | RNA-P6T1-P6T1-4 | Human | Lung | MIAC | 1.36e-02 | 8.16e-01 | -0.0263 |
121256 | TMEM132D | RNA-P7T1-P7T1-1 | Human | Lung | AIS | 1.69e-05 | 7.75e-01 | -0.0961 |
121256 | TMEM132D | RNA-P7T1-P7T1-2 | Human | Lung | AIS | 5.59e-06 | 7.83e-01 | -0.0876 |
121256 | TMEM132D | RNA-P7T1-P7T1-3 | Human | Lung | AIS | 2.32e-05 | 7.21e-01 | -0.0822 |
121256 | TMEM132D | RNA-P7T1-P7T1-4 | Human | Lung | AIS | 1.09e-06 | 7.42e-01 | -0.0809 |
121256 | TMEM132D | HTA12-15-2 | Human | Pancreas | PDAC | 1.28e-15 | 1.01e+00 | 0.2315 |
121256 | TMEM132D | HTA12-16-2 | Human | Pancreas | PDAC | 1.71e-02 | 7.57e-01 | 0.0535 |
121256 | TMEM132D | HTA12-23-1 | Human | Pancreas | PDAC | 7.33e-25 | 1.57e+00 | 0.3405 |
121256 | TMEM132D | HTA12-25-1 | Human | Pancreas | PDAC | 9.43e-22 | 1.40e+00 | 0.313 |
121256 | TMEM132D | HTA12-26-1 | Human | Pancreas | PDAC | 2.17e-46 | 1.74e+00 | 0.3728 |
121256 | TMEM132D | HTA12-29-1 | Human | Pancreas | PDAC | 5.10e-104 | 1.69e+00 | 0.3722 |
121256 | TMEM132D | HTA12-30-1 | Human | Pancreas | PDAC | 6.56e-10 | 1.55e+00 | 0.3671 |
121256 | TMEM132D | HTA12-32-1 | Human | Pancreas | PDAC | 1.44e-13 | 1.70e+00 | 0.3624 |
121256 | TMEM132D | HTA12-9-1 | Human | Pancreas | PDAC | 3.82e-02 | 2.81e-01 | 0.1532 |
121256 | TMEM132D | HTA12-9-2 | Human | Pancreas | PDAC | 1.65e-02 | 2.37e-01 | 0.0835 |
121256 | TMEM132D | HTA12-9-3 | Human | Pancreas | PDAC | 1.07e-02 | 5.51e-01 | 0.2045 |
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Tissue | Expression Dynamics | Abbreviation |
Lung | ![]() | AAH: Atypical adenomatous hyperplasia |
AIS: Adenocarcinoma in situ | ||
IAC: Invasive lung adenocarcinoma | ||
MIA: Minimally invasive adenocarcinoma |
∗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 |
TMEM132D | SNV | Missense_Mutation | rs138850997 | c.730G>A | p.Ala244Thr | p.A244T | Q14C87 | protein_coding | tolerated(0.41) | benign(0.001) | TCGA-NH-A5IV-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TMEM132D | SNV | Missense_Mutation | c.2789N>T | p.Ala930Val | p.A930V | Q14C87 | protein_coding | deleterious(0) | probably_damaging(0.962) | TCGA-QL-A97D-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
TMEM132D | SNV | Missense_Mutation | c.2193N>A | p.Phe731Leu | p.F731L | Q14C87 | protein_coding | tolerated(0.05) | possibly_damaging(0.84) | TCGA-AF-A56N-01 | Colorectum | rectum adenocarcinoma | Female | <65 | I/II | Chemotherapy | xeloda | CR | |
TMEM132D | SNV | Missense_Mutation | novel | c.1884N>T | p.Gln628His | p.Q628H | Q14C87 | protein_coding | deleterious(0.04) | possibly_damaging(0.66) | TCGA-AG-3727-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
TMEM132D | SNV | Missense_Mutation | c.331A>G | p.Met111Val | p.M111V | Q14C87 | protein_coding | tolerated(0.17) | benign(0.001) | TCGA-AG-3728-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | folinic | CR | |
TMEM132D | SNV | Missense_Mutation | c.1732C>T | p.Arg578Trp | p.R578W | Q14C87 | protein_coding | deleterious(0) | probably_damaging(0.984) | TCGA-AG-3883-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
TMEM132D | SNV | Missense_Mutation | rs761917469 | c.3169G>A | p.Asp1057Asn | p.D1057N | Q14C87 | protein_coding | tolerated(0.21) | benign(0.131) | TCGA-AG-3902-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
TMEM132D | SNV | Missense_Mutation | novel | c.2534N>A | p.Ser845Tyr | p.S845Y | Q14C87 | protein_coding | deleterious(0) | possibly_damaging(0.509) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
TMEM132D | SNV | Missense_Mutation | novel | c.497N>T | p.Pro166Leu | p.P166L | Q14C87 | protein_coding | deleterious(0.03) | probably_damaging(1) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
TMEM132D | SNV | Missense_Mutation | c.1680N>G | p.Asp560Glu | p.D560E | Q14C87 | protein_coding | tolerated(0.91) | benign(0.003) | TCGA-AG-A020-01 | Colorectum | rectum adenocarcinoma | Female | <65 | III/IV | Chemotherapy | folinic | CR |
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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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