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Gene: LSAMP |
Gene summary for LSAMP |
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Gene information | Species | Human | Gene symbol | LSAMP | Gene ID | 4045 |
Gene name | limbic system associated membrane protein | |
Gene Alias | IGLON3 | |
Cytomap | 3q13.31 | |
Gene Type | protein-coding | GO ID | GO:0007155 | UniProtAcc | B7Z661 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
4045 | LSAMP | HTA11_2487_2000001011 | Human | Colorectum | SER | 4.35e-03 | 3.35e-01 | -0.1808 |
4045 | LSAMP | HTA11_78_2000001011 | Human | Colorectum | AD | 2.84e-02 | 2.38e-01 | -0.1088 |
4045 | LSAMP | HTA11_347_2000001011 | Human | Colorectum | AD | 2.60e-02 | 2.03e-01 | -0.1954 |
4045 | LSAMP | HTA11_3361_2000001011 | Human | Colorectum | AD | 3.18e-02 | 2.63e-01 | -0.1207 |
4045 | LSAMP | HTA11_696_2000001011 | Human | Colorectum | AD | 2.81e-02 | 2.06e-01 | -0.1464 |
4045 | LSAMP | HTA11_866_2000001011 | Human | Colorectum | AD | 5.44e-03 | 1.81e-01 | -0.1001 |
4045 | LSAMP | HTA11_1391_2000001011 | Human | Colorectum | AD | 5.73e-05 | 3.75e-01 | -0.059 |
4045 | LSAMP | HTA11_6818_2000001011 | Human | Colorectum | AD | 1.44e-02 | 3.75e-01 | 0.0112 |
4045 | LSAMP | HTA11_6818_2000001021 | Human | Colorectum | AD | 1.60e-14 | 8.62e-01 | 0.0588 |
4045 | LSAMP | HTA11_99999970781_79442 | Human | Colorectum | MSS | 2.31e-04 | 4.61e-01 | 0.294 |
4045 | LSAMP | HTA11_99999965104_69814 | Human | Colorectum | MSS | 6.34e-27 | 1.15e+00 | 0.281 |
4045 | LSAMP | CRC-3-11773 | Human | Colorectum | CRC | 2.14e-06 | 5.06e-01 | 0.2564 |
4045 | LSAMP | C38 | Human | Oral cavity | OSCC | 1.46e-04 | 7.64e-01 | 0.172 |
4045 | LSAMP | NEOLP-1 | Human | Oral cavity | NEOLP | 3.20e-22 | 8.41e-01 | -0.0194 |
4045 | LSAMP | NEOLP-2 | Human | Oral cavity | NEOLP | 1.83e-02 | 3.03e-01 | -0.0196 |
4045 | LSAMP | HTA12-15-2 | Human | Pancreas | PDAC | 4.32e-07 | 6.06e-01 | 0.2315 |
4045 | LSAMP | HTA12-18-3 | Human | Pancreas | PDAC | 4.07e-03 | 6.29e-01 | 0.0716 |
4045 | LSAMP | HTA12-23-1 | Human | Pancreas | PDAC | 1.06e-18 | 1.41e+00 | 0.3405 |
4045 | LSAMP | HTA12-25-1 | Human | Pancreas | PDAC | 2.04e-11 | 9.03e-01 | 0.313 |
4045 | LSAMP | HTA12-26-1 | Human | Pancreas | PDAC | 1.81e-32 | 1.39e+00 | 0.3728 |
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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 |
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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 |
LSAMP | SNV | Missense_Mutation | rs569392861 | c.827N>T | p.Thr276Met | p.T276M | Q13449 | protein_coding | tolerated(0.37) | benign(0.15) | TCGA-CK-4948-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
LSAMP | SNV | Missense_Mutation | c.578G>A | p.Gly193Asp | p.G193D | Q13449 | protein_coding | deleterious(0.01) | probably_damaging(0.998) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
LSAMP | SNV | Missense_Mutation | c.856N>A | p.Gly286Ser | p.G286S | Q13449 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-G4-6309-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Chemotherapy | xeloda | PD | |
LSAMP | SNV | Missense_Mutation | c.290G>A | p.Arg97Gln | p.R97Q | Q13449 | protein_coding | tolerated(1) | benign(0.058) | TCGA-A5-A0GP-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
LSAMP | SNV | Missense_Mutation | novel | c.297N>T | p.Gln99His | p.Q99H | Q13449 | protein_coding | tolerated(0.12) | benign(0.223) | TCGA-AJ-A5DW-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
LSAMP | SNV | Missense_Mutation | novel | c.145N>T | p.Ala49Ser | p.A49S | Q13449 | protein_coding | deleterious(0.04) | benign(0.1) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
LSAMP | SNV | Missense_Mutation | c.25N>T | p.Arg9Trp | p.R9W | Q13449 | protein_coding | deleterious_low_confidence(0.03) | benign(0) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
LSAMP | SNV | Missense_Mutation | novel | c.1003N>T | p.Leu335Phe | p.L335F | Q13449 | protein_coding | tolerated(0.47) | benign(0.003) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
LSAMP | SNV | Missense_Mutation | novel | c.242A>G | p.Asp81Gly | p.D81G | Q13449 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AP-A1DK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
LSAMP | SNV | Missense_Mutation | rs765460014 | c.617N>T | p.Ala206Val | p.A206V | Q13449 | protein_coding | deleterious(0.04) | possibly_damaging(0.837) | TCGA-AP-A1DV-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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