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Gene: MAN2B2 |
Gene summary for MAN2B2 |
Gene summary. |
Gene information | Species | Human | Gene symbol | MAN2B2 | Gene ID | 23324 |
Gene name | mannosidase alpha class 2B member 2 | |
Gene Alias | MAN2B2 | |
Cytomap | 4p16.1 | |
Gene Type | protein-coding | GO ID | GO:0005975 | UniProtAcc | B7Z754 |
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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 |
23324 | MAN2B2 | HTA11_3410_2000001011 | Human | Colorectum | AD | 5.38e-43 | 8.95e-01 | 0.0155 |
23324 | MAN2B2 | HTA11_2487_2000001011 | Human | Colorectum | SER | 1.91e-29 | 9.31e-01 | -0.1808 |
23324 | MAN2B2 | HTA11_2951_2000001011 | Human | Colorectum | AD | 2.80e-10 | 9.09e-01 | 0.0216 |
23324 | MAN2B2 | HTA11_1938_2000001011 | Human | Colorectum | AD | 1.86e-39 | 1.56e+00 | -0.0811 |
23324 | MAN2B2 | HTA11_78_2000001011 | Human | Colorectum | AD | 1.79e-07 | 4.05e-01 | -0.1088 |
23324 | MAN2B2 | HTA11_347_2000001011 | Human | Colorectum | AD | 1.07e-34 | 8.50e-01 | -0.1954 |
23324 | MAN2B2 | HTA11_411_2000001011 | Human | Colorectum | SER | 3.97e-16 | 1.35e+00 | -0.2602 |
23324 | MAN2B2 | HTA11_2112_2000001011 | Human | Colorectum | SER | 2.41e-17 | 1.47e+00 | -0.2196 |
23324 | MAN2B2 | HTA11_3361_2000001011 | Human | Colorectum | AD | 3.77e-27 | 9.58e-01 | -0.1207 |
23324 | MAN2B2 | HTA11_83_2000001011 | Human | Colorectum | SER | 8.63e-35 | 1.36e+00 | -0.1526 |
23324 | MAN2B2 | HTA11_696_2000001011 | Human | Colorectum | AD | 3.51e-94 | 1.66e+00 | -0.1464 |
23324 | MAN2B2 | HTA11_866_2000001011 | Human | Colorectum | AD | 9.19e-42 | 9.01e-01 | -0.1001 |
23324 | MAN2B2 | HTA11_1391_2000001011 | Human | Colorectum | AD | 1.76e-54 | 1.40e+00 | -0.059 |
23324 | MAN2B2 | HTA11_2992_2000001011 | Human | Colorectum | SER | 8.04e-23 | 1.13e+00 | -0.1706 |
23324 | MAN2B2 | HTA11_5212_2000001011 | Human | Colorectum | AD | 3.44e-25 | 1.30e+00 | -0.2061 |
23324 | MAN2B2 | HTA11_5216_2000001011 | Human | Colorectum | SER | 3.59e-25 | 1.44e+00 | -0.1462 |
23324 | MAN2B2 | HTA11_546_2000001011 | Human | Colorectum | AD | 1.41e-15 | 7.96e-01 | -0.0842 |
23324 | MAN2B2 | HTA11_9341_2000001011 | Human | Colorectum | SER | 6.47e-03 | 6.44e-01 | -0.00410000000000005 |
23324 | MAN2B2 | HTA11_7862_2000001011 | Human | Colorectum | AD | 1.24e-07 | 4.82e-01 | -0.0179 |
23324 | MAN2B2 | HTA11_866_3004761011 | Human | Colorectum | AD | 2.25e-15 | 5.37e-01 | 0.096 |
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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:0019318 | Colorectum | AD | hexose metabolic process | 77/3918 | 237/18723 | 1.96e-05 | 4.01e-04 | 77 |
GO:0005996 | Colorectum | AD | monosaccharide metabolic process | 80/3918 | 257/18723 | 7.31e-05 | 1.17e-03 | 80 |
GO:00193181 | Colorectum | SER | hexose metabolic process | 56/2897 | 237/18723 | 6.19e-04 | 8.42e-03 | 56 |
GO:00059961 | Colorectum | SER | monosaccharide metabolic process | 59/2897 | 257/18723 | 9.65e-04 | 1.15e-02 | 59 |
GO:00193182 | Colorectum | MSS | hexose metabolic process | 63/3467 | 237/18723 | 1.32e-03 | 1.25e-02 | 63 |
GO:00059962 | Colorectum | MSS | monosaccharide metabolic process | 66/3467 | 257/18723 | 2.61e-03 | 2.06e-02 | 66 |
GO:00059969 | Esophagus | ESCC | monosaccharide metabolic process | 159/8552 | 257/18723 | 1.11e-07 | 1.81e-06 | 159 |
GO:00193189 | Esophagus | ESCC | hexose metabolic process | 147/8552 | 237/18723 | 2.63e-07 | 3.94e-06 | 147 |
GO:000599621 | Liver | HCC | monosaccharide metabolic process | 167/7958 | 257/18723 | 2.31e-13 | 1.25e-11 | 167 |
GO:001931821 | Liver | HCC | hexose metabolic process | 155/7958 | 237/18723 | 7.63e-13 | 3.90e-11 | 155 |
GO:001931810 | Thyroid | PTC | hexose metabolic process | 108/5968 | 237/18723 | 6.42e-06 | 7.65e-05 | 108 |
GO:000599614 | Thyroid | PTC | monosaccharide metabolic process | 115/5968 | 257/18723 | 9.36e-06 | 1.05e-04 | 115 |
GO:001931814 | Thyroid | ATC | hexose metabolic process | 111/6293 | 237/18723 | 1.51e-05 | 1.41e-04 | 111 |
GO:000599615 | Thyroid | ATC | monosaccharide metabolic process | 118/6293 | 257/18723 | 2.56e-05 | 2.20e-04 | 118 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa00511 | Liver | HCC | Other glycan degradation | 15/4020 | 18/8465 | 1.96e-03 | 6.91e-03 | 3.84e-03 | 15 |
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 |
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 |
MAN2B2 | SNV | Missense_Mutation | c.2211N>C | p.Gln737His | p.Q737H | Q9Y2E5 | protein_coding | deleterious(0) | probably_damaging(0.983) | TCGA-IR-A3LK-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | PD | |
MAN2B2 | SNV | Missense_Mutation | c.925N>T | p.Ile309Phe | p.I309F | Q9Y2E5 | protein_coding | deleterious(0) | probably_damaging(0.943) | TCGA-JW-A5VI-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | topotecan | PD | |
MAN2B2 | SNV | Missense_Mutation | c.1787N>A | p.Thr596Asn | p.T596N | Q9Y2E5 | protein_coding | deleterious(0.02) | benign(0.358) | TCGA-AA-3819-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
MAN2B2 | SNV | Missense_Mutation | novel | c.751N>C | p.Ser251Arg | p.S251R | Q9Y2E5 | protein_coding | tolerated(0.05) | possibly_damaging(0.732) | TCGA-AA-3950-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MAN2B2 | SNV | Missense_Mutation | rs145945260 | c.1714N>T | p.Arg572Cys | p.R572C | Q9Y2E5 | protein_coding | tolerated(0.1) | possibly_damaging(0.636) | TCGA-AZ-6601-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
MAN2B2 | SNV | Missense_Mutation | rs148186055 | c.971C>T | p.Thr324Met | p.T324M | Q9Y2E5 | protein_coding | deleterious(0) | probably_damaging(0.96) | TCGA-CK-5913-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
MAN2B2 | SNV | Missense_Mutation | c.1018C>T | p.Arg340Cys | p.R340C | Q9Y2E5 | protein_coding | deleterious(0.05) | benign(0.007) | TCGA-F4-6856-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Ancillary | leucovorin | CR | |
MAN2B2 | SNV | Missense_Mutation | rs200380914 | c.2828N>T | p.Ala943Val | p.A943V | Q9Y2E5 | protein_coding | deleterious(0.04) | benign(0.418) | TCGA-G4-6294-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | fluorouracil | PD |
MAN2B2 | SNV | Missense_Mutation | c.2387N>A | p.Arg796Gln | p.R796Q | Q9Y2E5 | protein_coding | deleterious(0.05) | probably_damaging(0.94) | TCGA-NH-A5IV-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MAN2B2 | SNV | Missense_Mutation | rs781403225 | c.2756N>G | p.His919Arg | p.H919R | Q9Y2E5 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-WS-AB45-01 | Colorectum | colon adenocarcinoma | Female | <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 |
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