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Gene: MRAP2 |
Gene summary for MRAP2 |
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Gene information | Species | Human | Gene symbol | MRAP2 | Gene ID | 112609 |
Gene name | melanocortin 2 receptor accessory protein 2 | |
Gene Alias | C6orf117 | |
Cytomap | 6q14.2 | |
Gene Type | protein-coding | GO ID | GO:0006091 | UniProtAcc | Q96G30 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
112609 | MRAP2 | P2T-E | Human | Esophagus | ESCC | 1.22e-08 | 1.68e-01 | 0.1177 |
112609 | MRAP2 | P4T-E | Human | Esophagus | ESCC | 3.41e-12 | 3.36e-01 | 0.1323 |
112609 | MRAP2 | P9T-E | Human | Esophagus | ESCC | 7.92e-12 | 2.74e-01 | 0.1131 |
112609 | MRAP2 | P10T-E | Human | Esophagus | ESCC | 1.15e-10 | 3.20e-01 | 0.116 |
112609 | MRAP2 | P15T-E | Human | Esophagus | ESCC | 1.83e-08 | 2.80e-01 | 0.1149 |
112609 | MRAP2 | P20T-E | Human | Esophagus | ESCC | 3.11e-02 | 1.18e-01 | 0.1124 |
112609 | MRAP2 | P22T-E | Human | Esophagus | ESCC | 1.32e-05 | 1.31e-01 | 0.1236 |
112609 | MRAP2 | P23T-E | Human | Esophagus | ESCC | 1.84e-03 | 1.47e-01 | 0.108 |
112609 | MRAP2 | P27T-E | Human | Esophagus | ESCC | 8.14e-09 | 1.82e-01 | 0.1055 |
112609 | MRAP2 | P28T-E | Human | Esophagus | ESCC | 3.16e-14 | 3.21e-01 | 0.1149 |
112609 | MRAP2 | P30T-E | Human | Esophagus | ESCC | 8.40e-21 | 8.52e-01 | 0.137 |
112609 | MRAP2 | P31T-E | Human | Esophagus | ESCC | 2.28e-03 | 1.33e-01 | 0.1251 |
112609 | MRAP2 | P39T-E | Human | Esophagus | ESCC | 2.03e-12 | 2.53e-01 | 0.0894 |
112609 | MRAP2 | P42T-E | Human | Esophagus | ESCC | 4.97e-04 | 1.68e-01 | 0.1175 |
112609 | MRAP2 | P48T-E | Human | Esophagus | ESCC | 6.03e-09 | 2.29e-01 | 0.0959 |
112609 | MRAP2 | P52T-E | Human | Esophagus | ESCC | 1.24e-08 | 3.90e-01 | 0.1555 |
112609 | MRAP2 | P54T-E | Human | Esophagus | ESCC | 1.58e-02 | 1.27e-01 | 0.0975 |
112609 | MRAP2 | P65T-E | Human | Esophagus | ESCC | 8.90e-03 | 6.50e-02 | 0.0978 |
112609 | MRAP2 | P74T-E | Human | Esophagus | ESCC | 2.12e-02 | 9.90e-02 | 0.1479 |
112609 | MRAP2 | P128T-E | Human | Esophagus | ESCC | 1.28e-29 | 8.41e-01 | 0.1241 |
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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 |
Breast | Precancer | ![]() |
Breast | IDC | ![]() |
Breast | DCIS | ![]() |
Cervix | CC | ![]() |
Cervix | HSIL_HPV | ![]() |
∗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:0006091110 | Esophagus | ESCC | generation of precursor metabolites and energy | 331/8552 | 490/18723 | 3.86e-23 | 8.45e-21 | 331 |
GO:0015980110 | Esophagus | ESCC | energy derivation by oxidation of organic compounds | 220/8552 | 318/18723 | 1.20e-17 | 1.09e-15 | 220 |
GO:0072659110 | Esophagus | ESCC | protein localization to plasma membrane | 193/8552 | 284/18723 | 1.95e-14 | 1.03e-12 | 193 |
GO:199077819 | Esophagus | ESCC | protein localization to cell periphery | 217/8552 | 333/18723 | 4.08e-13 | 1.88e-11 | 217 |
GO:190547519 | Esophagus | ESCC | regulation of protein localization to membrane | 117/8552 | 175/18723 | 1.14e-08 | 2.26e-07 | 117 |
GO:190437519 | Esophagus | ESCC | regulation of protein localization to cell periphery | 85/8552 | 125/18723 | 3.63e-07 | 5.06e-06 | 85 |
GO:1903076110 | Esophagus | ESCC | regulation of protein localization to plasma membrane | 72/8552 | 104/18723 | 9.74e-07 | 1.23e-05 | 72 |
GO:19038289 | Esophagus | ESCC | negative regulation of cellular protein localization | 76/8552 | 117/18723 | 1.97e-05 | 1.72e-04 | 76 |
GO:19030778 | Esophagus | ESCC | negative regulation of protein localization to plasma membrane | 17/8552 | 24/18723 | 1.13e-02 | 3.81e-02 | 17 |
GO:19043765 | Esophagus | ESCC | negative regulation of protein localization to cell periphery | 18/8552 | 26/18723 | 1.32e-02 | 4.31e-02 | 18 |
GO:000609118 | Oral cavity | OSCC | generation of precursor metabolites and energy | 286/7305 | 490/18723 | 1.45e-18 | 1.71e-16 | 286 |
GO:001598018 | Oral cavity | OSCC | energy derivation by oxidation of organic compounds | 190/7305 | 318/18723 | 4.10e-14 | 2.26e-12 | 190 |
GO:007265918 | Oral cavity | OSCC | protein localization to plasma membrane | 169/7305 | 284/18723 | 1.69e-12 | 7.21e-11 | 169 |
GO:199077816 | Oral cavity | OSCC | protein localization to cell periphery | 190/7305 | 333/18723 | 1.46e-11 | 5.13e-10 | 190 |
GO:190547516 | Oral cavity | OSCC | regulation of protein localization to membrane | 105/7305 | 175/18723 | 1.42e-08 | 2.85e-07 | 105 |
GO:190437516 | Oral cavity | OSCC | regulation of protein localization to cell periphery | 78/7305 | 125/18723 | 9.80e-08 | 1.68e-06 | 78 |
GO:190307617 | Oral cavity | OSCC | regulation of protein localization to plasma membrane | 67/7305 | 104/18723 | 1.34e-07 | 2.24e-06 | 67 |
GO:19038288 | Oral cavity | OSCC | negative regulation of cellular protein localization | 65/7305 | 117/18723 | 2.05e-04 | 1.36e-03 | 65 |
GO:19030777 | Oral cavity | OSCC | negative regulation of protein localization to plasma membrane | 16/7305 | 24/18723 | 5.63e-03 | 2.17e-02 | 16 |
GO:19054764 | Oral cavity | OSCC | negative regulation of protein localization to membrane | 19/7305 | 32/18723 | 1.56e-02 | 5.00e-02 | 19 |
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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 |
MRAP2 | insertion | Nonsense_Mutation | novel | c.483_484insCTACACTAGAATTGAATGTTGGAATCTAAAACAGGTGCCATCT | p.Met162LeufsTer3 | p.M162Lfs*3 | Q96G30 | protein_coding | TCGA-C8-A12L-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
MRAP2 | deletion | In_Frame_Del | novel | c.559_582delNNNNNNNNNNNNNNNNNNNNNNNN | p.Pro188_Pro195del | p.P188_P195del | Q96G30 | protein_coding | TCGA-C5-A8XH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | ||
MRAP2 | SNV | Missense_Mutation | c.400N>A | p.Gln134Lys | p.Q134K | Q96G30 | protein_coding | tolerated(1) | benign(0) | TCGA-A6-6650-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MRAP2 | SNV | Missense_Mutation | c.39G>T | p.Gln13His | p.Q13H | Q96G30 | protein_coding | tolerated(0.13) | benign(0.001) | TCGA-AA-3818-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
MRAP2 | SNV | Missense_Mutation | c.125A>C | p.Lys42Thr | p.K42T | Q96G30 | protein_coding | deleterious(0.01) | possibly_damaging(0.776) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
MRAP2 | SNV | Missense_Mutation | c.246N>T | p.Glu82Asp | p.E82D | Q96G30 | protein_coding | tolerated(0.13) | possibly_damaging(0.543) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
MRAP2 | SNV | Missense_Mutation | novel | c.455N>T | p.Gly152Val | p.G152V | Q96G30 | protein_coding | deleterious(0.01) | benign(0.109) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
MRAP2 | SNV | Missense_Mutation | novel | c.295G>A | p.Glu99Lys | p.E99K | Q96G30 | protein_coding | tolerated(0.14) | benign(0.017) | TCGA-AA-A004-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
MRAP2 | SNV | Missense_Mutation | c.512A>T | p.Asn171Ile | p.N171I | Q96G30 | protein_coding | deleterious(0) | possibly_damaging(0.823) | TCGA-AM-5821-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MRAP2 | SNV | Missense_Mutation | rs148904867 | c.373N>T | p.Arg125Cys | p.R125C | Q96G30 | protein_coding | deleterious(0.02) | benign(0.311) | TCGA-AZ-6599-01 | Colorectum | colon adenocarcinoma | Male | >=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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