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Gene: GHRL |
Gene summary for GHRL |
Gene summary. |
Gene information | Species | Human | Gene symbol | GHRL | Gene ID | 51738 |
Gene name | ghrelin and obestatin prepropeptide | |
Gene Alias | MTLRP | |
Cytomap | 3p25.3 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | Q9UBU3 |
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Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
51738 | GHRL | Pat02-B | Human | Stomach | GC | 1.59e-06 | 2.39e-02 | 0.0368 |
51738 | GHRL | Pat05-B | Human | Stomach | GC | 4.22e-05 | 1.48e-01 | -0.0353 |
51738 | GHRL | Pat06-B | Human | Stomach | GC | 6.41e-47 | 4.35e-01 | -0.1961 |
51738 | GHRL | Pat15-B | Human | Stomach | GC | 6.61e-09 | 2.43e-01 | -0.0778 |
51738 | GHRL | Pat24-B | Human | Stomach | GC | 2.39e-74 | 1.30e+00 | -0.1184 |
51738 | GHRL | Pat28-A | Human | Stomach | CSG | 3.50e-17 | 3.10e-01 | -0.2594 |
51738 | GHRL | Pat29-A | Human | Stomach | CAG with IM | 1.92e-44 | 1.13e+00 | -0.2769 |
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Transcriptomic changes along malignancy continuum. |
∗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 |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
Figure of enriched GO biological processes. |
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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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00516022 | Stomach | CSG | response to electrical stimulus | 8/1034 | 42/18723 | 1.86e-03 | 1.97e-02 | 8 |
GO:005070821 | Stomach | CSG | regulation of protein secretion | 27/1034 | 268/18723 | 1.92e-03 | 2.02e-02 | 27 |
GO:00506791 | Stomach | CSG | positive regulation of epithelial cell proliferation | 22/1034 | 207/18723 | 2.51e-03 | 2.46e-02 | 22 |
GO:004343421 | Stomach | CSG | response to peptide hormone | 37/1034 | 414/18723 | 2.75e-03 | 2.62e-02 | 37 |
GO:001583321 | Stomach | CSG | peptide transport | 26/1034 | 264/18723 | 3.14e-03 | 2.92e-02 | 26 |
GO:009025711 | Stomach | CSG | regulation of muscle system process | 25/1034 | 252/18723 | 3.39e-03 | 3.06e-02 | 25 |
GO:003432921 | Stomach | CSG | cell junction assembly | 37/1034 | 420/18723 | 3.50e-03 | 3.15e-02 | 37 |
GO:003007321 | Stomach | CSG | insulin secretion | 20/1034 | 195/18723 | 5.72e-03 | 4.55e-02 | 20 |
GO:00069373 | Stomach | CSG | regulation of muscle contraction | 18/1034 | 169/18723 | 5.77e-03 | 4.59e-02 | 18 |
GO:000762311 | Stomach | CSG | circadian rhythm | 21/1034 | 210/18723 | 6.27e-03 | 4.86e-02 | 21 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
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 |
Annotation of somatic variants for genes involved in malignant transformation |
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 |
GHRL | SNV | Missense_Mutation | c.196N>A | p.Glu66Lys | p.E66K | Q9UBU3 | protein_coding | tolerated(0.12) | possibly_damaging(0.492) | TCGA-A8-A06Q-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
GHRL | SNV | Missense_Mutation | rs767976379 | c.187N>A | p.Gly63Ser | p.G63S | Q9UBU3 | protein_coding | tolerated(0.8) | benign(0.029) | TCGA-BH-A0EB-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD |
GHRL | SNV | Missense_Mutation | rs540101934 | c.40N>A | p.Gly14Ser | p.G14S | Q9UBU3 | protein_coding | tolerated(1) | benign(0) | TCGA-G4-6628-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
GHRL | SNV | Missense_Mutation | novel | c.122N>T | p.Ser41Leu | p.S41L | Q9UBU3 | protein_coding | tolerated(0.19) | possibly_damaging(0.448) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
GHRL | SNV | Missense_Mutation | novel | c.337G>T | p.Ala113Ser | p.A113S | Q9UBU3 | protein_coding | tolerated(0.23) | benign(0.272) | TCGA-AP-A1E1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
GHRL | SNV | Missense_Mutation | novel | c.290N>T | p.Ala97Val | p.A97V | Q9UBU3 | protein_coding | tolerated(0.29) | possibly_damaging(0.809) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD |
GHRL | SNV | Missense_Mutation | rs567867101 | c.173G>A | p.Arg58His | p.R58H | Q9UBU3 | protein_coding | tolerated(0.28) | benign(0) | TCGA-EO-A3KX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
GHRL | SNV | Missense_Mutation | novel | c.122C>T | p.Ser41Leu | p.S41L | Q9UBU3 | protein_coding | tolerated(0.19) | possibly_damaging(0.448) | TCGA-FI-A2D4-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatinum | PD |
GHRL | SNV | Missense_Mutation | rs372434370 | c.208N>T | p.Asp70Tyr | p.D70Y | Q9UBU3 | protein_coding | deleterious(0) | possibly_damaging(0.905) | TCGA-PG-A915-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
GHRL | SNV | Missense_Mutation | rs756969269 | c.178G>A | p.Glu60Lys | p.E60K | Q9UBU3 | protein_coding | tolerated(0.05) | possibly_damaging(0.689) | TCGA-90-A4ED-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
51738 | GHRL | DRUGGABLE GENOME | ROFECOXIB | ROFECOXIB | 16868036 | |
51738 | GHRL | DRUGGABLE GENOME | RALOXIFENE | RALOXIFENE | 18164562 | |
51738 | GHRL | DRUGGABLE GENOME | HUMAN CHORIONIC GONADOTROPIN | 17535999 | ||
51738 | GHRL | DRUGGABLE GENOME | PIOGLITAZONE | PIOGLITAZONE | 16682836 | |
51738 | GHRL | DRUGGABLE GENOME | Unacylated ghrelin | |||
51738 | GHRL | DRUGGABLE GENOME | RISPERIDONE | RISPERIDONE | 18480685 | |
51738 | GHRL | DRUGGABLE GENOME | Relamorelin | RELAMORELIN | ||
51738 | GHRL | DRUGGABLE GENOME | ARD-07 | MACIMORELIN | ||
51738 | GHRL | DRUGGABLE GENOME | PLANT STEROLS | 18066136 | ||
51738 | GHRL | DRUGGABLE GENOME | INSULIN | INSULIN | 17449920 |
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