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Gene: MANBAL |
Gene summary for MANBAL |
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Gene information | Species | Human | Gene symbol | MANBAL | Gene ID | 63905 |
Gene name | mannosidase beta like | |
Gene Alias | MANBAL | |
Cytomap | 20q11.23 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | Q9NQG1 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
63905 | MANBAL | P20T-E | Human | Esophagus | ESCC | 1.16e-55 | 1.24e+00 | 0.1124 |
63905 | MANBAL | P21T-E | Human | Esophagus | ESCC | 5.48e-68 | 1.97e+00 | 0.1617 |
63905 | MANBAL | P22T-E | Human | Esophagus | ESCC | 7.30e-45 | 9.53e-01 | 0.1236 |
63905 | MANBAL | P23T-E | Human | Esophagus | ESCC | 1.42e-37 | 1.07e+00 | 0.108 |
63905 | MANBAL | P24T-E | Human | Esophagus | ESCC | 9.15e-22 | 6.47e-01 | 0.1287 |
63905 | MANBAL | P26T-E | Human | Esophagus | ESCC | 1.02e-76 | 1.50e+00 | 0.1276 |
63905 | MANBAL | P27T-E | Human | Esophagus | ESCC | 1.68e-24 | 5.98e-01 | 0.1055 |
63905 | MANBAL | P28T-E | Human | Esophagus | ESCC | 9.74e-18 | 3.56e-01 | 0.1149 |
63905 | MANBAL | P30T-E | Human | Esophagus | ESCC | 4.09e-37 | 1.29e+00 | 0.137 |
63905 | MANBAL | P31T-E | Human | Esophagus | ESCC | 1.28e-64 | 1.15e+00 | 0.1251 |
63905 | MANBAL | P32T-E | Human | Esophagus | ESCC | 1.70e-46 | 9.62e-01 | 0.1666 |
63905 | MANBAL | P36T-E | Human | Esophagus | ESCC | 4.06e-13 | 6.69e-01 | 0.1187 |
63905 | MANBAL | P37T-E | Human | Esophagus | ESCC | 5.20e-29 | 6.26e-01 | 0.1371 |
63905 | MANBAL | P38T-E | Human | Esophagus | ESCC | 7.62e-10 | 6.12e-01 | 0.127 |
63905 | MANBAL | P39T-E | Human | Esophagus | ESCC | 4.50e-20 | 4.09e-01 | 0.0894 |
63905 | MANBAL | P40T-E | Human | Esophagus | ESCC | 1.88e-19 | 4.03e-01 | 0.109 |
63905 | MANBAL | P42T-E | Human | Esophagus | ESCC | 4.83e-31 | 8.20e-01 | 0.1175 |
63905 | MANBAL | P44T-E | Human | Esophagus | ESCC | 4.06e-13 | 4.85e-01 | 0.1096 |
63905 | MANBAL | P47T-E | Human | Esophagus | ESCC | 8.02e-28 | 5.53e-01 | 0.1067 |
63905 | MANBAL | P48T-E | Human | Esophagus | ESCC | 1.35e-16 | 4.11e-01 | 0.0959 |
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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 |
MANBAL | SNV | Missense_Mutation | rs139446010 | c.67N>T | p.Arg23Trp | p.R23W | Q9NQG1 | protein_coding | tolerated(0.07) | probably_damaging(0.998) | TCGA-A8-A09M-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | paclitaxel | CR |
MANBAL | SNV | Missense_Mutation | c.74N>A | p.Gly25Glu | p.G25E | Q9NQG1 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A6-2686-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MANBAL | SNV | Missense_Mutation | rs139446010 | c.67N>T | p.Arg23Trp | p.R23W | Q9NQG1 | protein_coding | tolerated(0.07) | probably_damaging(0.998) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
MANBAL | SNV | Missense_Mutation | rs755003934 | c.29N>T | p.Pro10Leu | p.P10L | Q9NQG1 | protein_coding | deleterious_low_confidence(0) | probably_damaging(0.999) | TCGA-AJ-A3OK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Chemotherapy | carboplatin | CR |
MANBAL | SNV | Missense_Mutation | novel | c.201N>T | p.Lys67Asn | p.K67N | Q9NQG1 | protein_coding | deleterious(0.02) | possibly_damaging(0.587) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
MANBAL | SNV | Missense_Mutation | rs777773368 | c.124G>A | p.Val42Ile | p.V42I | Q9NQG1 | protein_coding | tolerated(1) | benign(0.001) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD |
MANBAL | SNV | Missense_Mutation | rs777773368 | c.124G>A | p.Val42Ile | p.V42I | Q9NQG1 | protein_coding | tolerated(1) | benign(0.001) | TCGA-E6-A1LX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
MANBAL | SNV | Missense_Mutation | rs747541266 | c.145N>A | p.Glu49Lys | p.E49K | Q9NQG1 | protein_coding | tolerated(0.32) | benign(0.265) | TCGA-49-6743-01 | Lung | lung adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | cisplatin | SD |
MANBAL | SNV | Missense_Mutation | rs755003934 | c.29C>T | p.Pro10Leu | p.P10L | Q9NQG1 | protein_coding | deleterious_low_confidence(0) | probably_damaging(0.999) | TCGA-18-3407-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
MANBAL | SNV | Missense_Mutation | c.230N>T | p.Pro77Leu | p.P77L | Q9NQG1 | protein_coding | tolerated(0.22) | benign(0.144) | TCGA-63-5131-01 | Lung | lung squamous cell carcinoma | Male | Unknown | 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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