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Gene: RAMP2 |
Gene summary for RAMP2 |
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Gene information | Species | Human | Gene symbol | RAMP2 | Gene ID | 10266 |
Gene name | receptor activity modifying protein 2 | |
Gene Alias | RAMP2 | |
Cytomap | 17q21.2 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | A0A024R1Z2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
10266 | RAMP2 | LZE4T | Human | Esophagus | ESCC | 5.33e-04 | 6.73e-02 | 0.0811 |
10266 | RAMP2 | LZE24T | Human | Esophagus | ESCC | 6.56e-11 | 4.15e-01 | 0.0596 |
10266 | RAMP2 | P2T-E | Human | Esophagus | ESCC | 2.42e-07 | 1.05e-01 | 0.1177 |
10266 | RAMP2 | P4T-E | Human | Esophagus | ESCC | 2.40e-10 | 5.41e-01 | 0.1323 |
10266 | RAMP2 | P8T-E | Human | Esophagus | ESCC | 7.25e-19 | 5.37e-01 | 0.0889 |
10266 | RAMP2 | P10T-E | Human | Esophagus | ESCC | 3.32e-09 | 2.22e-01 | 0.116 |
10266 | RAMP2 | P16T-E | Human | Esophagus | ESCC | 2.19e-48 | 9.42e-01 | 0.1153 |
10266 | RAMP2 | P20T-E | Human | Esophagus | ESCC | 3.85e-27 | 7.65e-01 | 0.1124 |
10266 | RAMP2 | P22T-E | Human | Esophagus | ESCC | 2.14e-36 | 5.74e-01 | 0.1236 |
10266 | RAMP2 | P23T-E | Human | Esophagus | ESCC | 1.80e-14 | 1.11e+00 | 0.108 |
10266 | RAMP2 | P24T-E | Human | Esophagus | ESCC | 5.00e-02 | 4.56e-01 | 0.1287 |
10266 | RAMP2 | P26T-E | Human | Esophagus | ESCC | 4.37e-37 | 6.70e-01 | 0.1276 |
10266 | RAMP2 | P27T-E | Human | Esophagus | ESCC | 4.91e-10 | 2.95e-01 | 0.1055 |
10266 | RAMP2 | P36T-E | Human | Esophagus | ESCC | 5.18e-06 | 8.26e-01 | 0.1187 |
10266 | RAMP2 | P38T-E | Human | Esophagus | ESCC | 1.30e-06 | 4.69e-01 | 0.127 |
10266 | RAMP2 | P47T-E | Human | Esophagus | ESCC | 6.33e-03 | 1.52e-01 | 0.1067 |
10266 | RAMP2 | P54T-E | Human | Esophagus | ESCC | 6.80e-05 | 3.30e-01 | 0.0975 |
10266 | RAMP2 | P56T-E | Human | Esophagus | ESCC | 1.38e-05 | 4.29e-01 | 0.1613 |
10266 | RAMP2 | P57T-E | Human | Esophagus | ESCC | 3.22e-02 | 1.72e-01 | 0.0926 |
10266 | RAMP2 | P61T-E | Human | Esophagus | ESCC | 1.64e-05 | 1.91e-01 | 0.099 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:0051098111 | Esophagus | ESCC | regulation of binding | 251/8552 | 363/18723 | 6.73e-20 | 8.46e-18 | 251 |
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:0051099111 | Esophagus | ESCC | positive regulation of binding | 122/8552 | 173/18723 | 2.79e-11 | 9.45e-10 | 122 |
GO:004339320 | Esophagus | ESCC | regulation of protein binding | 135/8552 | 196/18723 | 3.69e-11 | 1.22e-09 | 135 |
GO:0070482111 | Esophagus | ESCC | response to oxygen levels | 218/8552 | 347/18723 | 6.91e-11 | 2.17e-09 | 218 |
GO:0036293111 | Esophagus | ESCC | response to decreased oxygen levels | 201/8552 | 322/18723 | 8.37e-10 | 2.04e-08 | 201 |
GO:0001666111 | Esophagus | ESCC | response to hypoxia | 192/8552 | 307/18723 | 1.59e-09 | 3.69e-08 | 192 |
GO:0048545111 | Esophagus | ESCC | response to steroid hormone | 204/8552 | 339/18723 | 4.47e-08 | 8.11e-07 | 204 |
GO:003209216 | Esophagus | ESCC | positive regulation of protein binding | 60/8552 | 85/18723 | 2.83e-06 | 3.22e-05 | 60 |
GO:004311218 | Esophagus | ESCC | receptor metabolic process | 104/8552 | 166/18723 | 7.44e-06 | 7.37e-05 | 104 |
GO:1901654111 | Esophagus | ESCC | response to ketone | 118/8552 | 194/18723 | 1.45e-05 | 1.31e-04 | 118 |
GO:000689818 | Esophagus | ESCC | receptor-mediated endocytosis | 142/8552 | 244/18723 | 5.22e-05 | 4.05e-04 | 142 |
GO:00301984 | Esophagus | ESCC | extracellular matrix organization | 171/8552 | 301/18723 | 6.08e-05 | 4.67e-04 | 171 |
GO:00430624 | Esophagus | ESCC | extracellular structure organization | 171/8552 | 302/18723 | 7.73e-05 | 5.76e-04 | 171 |
GO:00452294 | Esophagus | ESCC | external encapsulating structure organization | 172/8552 | 304/18723 | 7.80e-05 | 5.80e-04 | 172 |
GO:003432918 | Esophagus | ESCC | cell junction assembly | 227/8552 | 420/18723 | 3.06e-04 | 1.83e-03 | 227 |
GO:004521620 | Esophagus | ESCC | cell-cell junction organization | 114/8552 | 200/18723 | 8.04e-04 | 4.16e-03 | 114 |
GO:004329718 | Esophagus | ESCC | apical junction assembly | 48/8552 | 78/18723 | 3.45e-03 | 1.41e-02 | 48 |
GO:00717115 | Esophagus | ESCC | basement membrane organization | 22/8552 | 31/18723 | 3.90e-03 | 1.58e-02 | 22 |
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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 |
RAMP2 | SNV | Missense_Mutation | rs369493002 | c.170C>T | p.Thr57Met | p.T57M | O60895 | protein_coding | tolerated(0.38) | benign(0.001) | TCGA-A6-5661-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
RAMP2 | insertion | Frame_Shift_Ins | novel | c.454_455insC | p.Ile154HisfsTer16 | p.I154Hfs*16 | O60895 | protein_coding | TCGA-AA-3713-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | 5-fluorouracil | PR | ||
RAMP2 | SNV | Missense_Mutation | novel | c.243N>T | p.Lys81Asn | p.K81N | O60895 | protein_coding | deleterious(0.03) | possibly_damaging(0.76) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
RAMP2 | SNV | Missense_Mutation | novel | c.427N>A | p.Glu143Lys | p.E143K | O60895 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-DF-A2KN-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | Unknown | I/II | Unknown | Unknown | SD |
RAMP2 | SNV | Missense_Mutation | novel | c.151C>T | p.Pro51Ser | p.P51S | O60895 | protein_coding | tolerated(0.44) | benign(0) | TCGA-EO-A22U-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
RAMP2 | SNV | Missense_Mutation | novel | c.200N>G | p.Phe67Cys | p.F67C | O60895 | protein_coding | tolerated(0.18) | possibly_damaging(0.455) | TCGA-EO-A22X-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unspecific | Carboplatin | Complete Response |
RAMP2 | SNV | Missense_Mutation | rs373990860 | c.238N>A | p.Glu80Lys | p.E80K | O60895 | protein_coding | tolerated(0.65) | benign(0) | TCGA-QS-A5YQ-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | CR |
RAMP2 | SNV | Missense_Mutation | novel | c.103C>A | p.Leu35Met | p.L35M | O60895 | protein_coding | deleterious(0.03) | probably_damaging(0.919) | TCGA-55-6979-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | PD |
RAMP2 | SNV | Missense_Mutation | c.170N>A | p.Thr57Lys | p.T57K | O60895 | protein_coding | tolerated(1) | benign(0.001) | TCGA-55-7907-01 | Lung | lung adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
RAMP2 | SNV | Missense_Mutation | novel | c.271N>G | p.Arg91Gly | p.R91G | O60895 | protein_coding | deleterious(0.01) | possibly_damaging(0.666) | TCGA-55-8089-01 | Lung | lung 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 |
10266 | RAMP2 | DRUGGABLE GENOME, CELL SURFACE | agonist | CHEMBL3833353 | PRAMLINTIDE ACETATE | |
10266 | RAMP2 | DRUGGABLE GENOME, CELL SURFACE | PRAMLINTIDE | PRAMLINTIDE | ||
10266 | RAMP2 | DRUGGABLE GENOME, CELL SURFACE | PRAMLINTIDE | PRAMLINTIDE |
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