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Gene: MANBA |
Gene summary for MANBA |
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Gene information | Species | Human | Gene symbol | MANBA | Gene ID | 4126 |
Gene name | mannosidase beta | |
Gene Alias | MANB1 | |
Cytomap | 4q24 | |
Gene Type | protein-coding | GO ID | GO:0005975 | UniProtAcc | O00462 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
4126 | MANBA | LZE7T | Human | Esophagus | ESCC | 7.20e-05 | 2.44e-01 | 0.0667 |
4126 | MANBA | LZE24T | Human | Esophagus | ESCC | 1.03e-12 | 3.76e-01 | 0.0596 |
4126 | MANBA | P1T-E | Human | Esophagus | ESCC | 6.78e-03 | 1.65e-01 | 0.0875 |
4126 | MANBA | P2T-E | Human | Esophagus | ESCC | 2.36e-07 | 1.45e-01 | 0.1177 |
4126 | MANBA | P4T-E | Human | Esophagus | ESCC | 2.45e-14 | 3.97e-01 | 0.1323 |
4126 | MANBA | P5T-E | Human | Esophagus | ESCC | 1.04e-02 | 1.28e-01 | 0.1327 |
4126 | MANBA | P8T-E | Human | Esophagus | ESCC | 9.22e-15 | 2.74e-01 | 0.0889 |
4126 | MANBA | P9T-E | Human | Esophagus | ESCC | 3.46e-10 | 2.09e-01 | 0.1131 |
4126 | MANBA | P10T-E | Human | Esophagus | ESCC | 1.99e-20 | 1.81e-01 | 0.116 |
4126 | MANBA | P11T-E | Human | Esophagus | ESCC | 2.59e-07 | 2.65e-01 | 0.1426 |
4126 | MANBA | P12T-E | Human | Esophagus | ESCC | 2.23e-08 | 1.70e-01 | 0.1122 |
4126 | MANBA | P15T-E | Human | Esophagus | ESCC | 1.48e-15 | 3.24e-01 | 0.1149 |
4126 | MANBA | P16T-E | Human | Esophagus | ESCC | 7.11e-10 | 1.78e-01 | 0.1153 |
4126 | MANBA | P20T-E | Human | Esophagus | ESCC | 3.31e-09 | 1.21e-01 | 0.1124 |
4126 | MANBA | P21T-E | Human | Esophagus | ESCC | 1.57e-02 | 1.54e-02 | 0.1617 |
4126 | MANBA | P22T-E | Human | Esophagus | ESCC | 1.65e-24 | 3.88e-01 | 0.1236 |
4126 | MANBA | P23T-E | Human | Esophagus | ESCC | 9.60e-07 | 2.67e-01 | 0.108 |
4126 | MANBA | P24T-E | Human | Esophagus | ESCC | 6.86e-16 | 8.26e-02 | 0.1287 |
4126 | MANBA | P26T-E | Human | Esophagus | ESCC | 1.10e-16 | 3.00e-01 | 0.1276 |
4126 | MANBA | P27T-E | Human | Esophagus | ESCC | 2.38e-17 | 3.31e-01 | 0.1055 |
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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 |
GO:00091002 | Esophagus | ESCC | glycoprotein metabolic process | 226/8552 | 387/18723 | 2.64e-07 | 3.94e-06 | 226 |
GO:001605216 | Esophagus | ESCC | carbohydrate catabolic process | 91/8552 | 154/18723 | 5.39e-04 | 2.97e-03 | 91 |
GO:19011362 | Esophagus | ESCC | carbohydrate derivative catabolic process | 99/8552 | 172/18723 | 1.11e-03 | 5.54e-03 | 99 |
GO:0006516 | Esophagus | ESCC | glycoprotein catabolic process | 19/8552 | 28/18723 | 1.49e-02 | 4.84e-02 | 19 |
GO:001605222 | Liver | HCC | carbohydrate catabolic process | 99/7958 | 154/18723 | 3.79e-08 | 8.30e-07 | 99 |
GO:1901136 | Liver | HCC | carbohydrate derivative catabolic process | 98/7958 | 172/18723 | 8.71e-05 | 7.62e-04 | 98 |
GO:0009100 | Liver | HCC | glycoprotein metabolic process | 193/7958 | 387/18723 | 1.89e-03 | 9.62e-03 | 193 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0414222 | Esophagus | ESCC | Lysosome | 102/4205 | 132/8465 | 5.11e-11 | 7.13e-10 | 3.65e-10 | 102 |
hsa0414232 | Esophagus | ESCC | Lysosome | 102/4205 | 132/8465 | 5.11e-11 | 7.13e-10 | 3.65e-10 | 102 |
hsa041422 | Liver | HCC | Lysosome | 100/4020 | 132/8465 | 2.32e-11 | 4.31e-10 | 2.40e-10 | 100 |
hsa00511 | Liver | HCC | Other glycan degradation | 15/4020 | 18/8465 | 1.96e-03 | 6.91e-03 | 3.84e-03 | 15 |
hsa041423 | Liver | HCC | Lysosome | 100/4020 | 132/8465 | 2.32e-11 | 4.31e-10 | 2.40e-10 | 100 |
hsa005111 | Liver | HCC | Other glycan degradation | 15/4020 | 18/8465 | 1.96e-03 | 6.91e-03 | 3.84e-03 | 15 |
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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 |
MANBA | SNV | Missense_Mutation | novel | c.2162G>A | p.Arg721Lys | p.R721K | O00462 | protein_coding | tolerated(0.75) | benign(0.005) | TCGA-PN-A8MA-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | SD |
MANBA | SNV | Missense_Mutation | c.842N>C | p.Ile281Thr | p.I281T | O00462 | protein_coding | deleterious(0) | possibly_damaging(0.852) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
MANBA | SNV | Missense_Mutation | c.1471N>C | p.Glu491Gln | p.E491Q | O00462 | protein_coding | tolerated(0.25) | benign(0.071) | TCGA-AA-A017-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
MANBA | SNV | Missense_Mutation | c.333N>A | p.Phe111Leu | p.F111L | O00462 | protein_coding | tolerated(1) | benign(0.001) | TCGA-AA-A03J-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MANBA | SNV | Missense_Mutation | rs145950049 | c.427N>T | p.Arg143Cys | p.R143C | O00462 | protein_coding | tolerated(0.12) | possibly_damaging(0.892) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD |
MANBA | SNV | Missense_Mutation | c.2321N>G | p.Tyr774Cys | p.Y774C | O00462 | protein_coding | tolerated(0.14) | benign(0.005) | TCGA-AD-A5EJ-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MANBA | SNV | Missense_Mutation | c.739N>A | p.Val247Ile | p.V247I | O00462 | protein_coding | tolerated(0.34) | benign(0.003) | TCGA-CM-6168-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MANBA | SNV | Missense_Mutation | rs561172083 | c.1477G>A | p.Val493Ile | p.V493I | O00462 | protein_coding | deleterious(0.05) | benign(0.125) | TCGA-AG-3893-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | folinic | CR |
MANBA | SNV | Missense_Mutation | rs757289997 | c.1097G>A | p.Arg366Gln | p.R366Q | O00462 | protein_coding | tolerated(0.14) | benign(0.124) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MANBA | SNV | Missense_Mutation | rs201237452 | c.397N>A | p.Val133Met | p.V133M | O00462 | protein_coding | tolerated(0.07) | benign(0.096) | TCGA-A5-A0GB-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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