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Gene: PSMB2 |
Gene summary for PSMB2 |
Gene summary. |
Gene information | Species | Human | Gene symbol | PSMB2 | Gene ID | 5690 |
Gene name | proteasome 20S subunit beta 2 | |
Gene Alias | HC7-I | |
Cytomap | 1p34.3 | |
Gene Type | protein-coding | GO ID | GO:0006508 | UniProtAcc | B7Z478 |
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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 |
5690 | PSMB2 | GSM4909281 | Human | Breast | IDC | 3.82e-02 | 3.06e-01 | 0.21 |
5690 | PSMB2 | GSM4909282 | Human | Breast | IDC | 4.20e-11 | 4.20e-01 | -0.0288 |
5690 | PSMB2 | GSM4909285 | Human | Breast | IDC | 2.36e-46 | 7.84e-01 | 0.21 |
5690 | PSMB2 | GSM4909287 | Human | Breast | IDC | 3.23e-02 | 2.94e-01 | 0.2057 |
5690 | PSMB2 | GSM4909288 | Human | Breast | IDC | 1.28e-04 | 3.21e-01 | 0.0988 |
5690 | PSMB2 | GSM4909294 | Human | Breast | IDC | 2.78e-02 | 5.06e-02 | 0.2022 |
5690 | PSMB2 | GSM4909296 | Human | Breast | IDC | 2.71e-08 | -2.78e-02 | 0.1524 |
5690 | PSMB2 | GSM4909297 | Human | Breast | IDC | 3.66e-14 | -2.24e-01 | 0.1517 |
5690 | PSMB2 | GSM4909298 | Human | Breast | IDC | 2.35e-02 | -2.42e-01 | 0.1551 |
5690 | PSMB2 | GSM4909311 | Human | Breast | IDC | 1.03e-26 | -2.36e-01 | 0.1534 |
5690 | PSMB2 | GSM4909312 | Human | Breast | IDC | 1.63e-11 | -2.42e-02 | 0.1552 |
5690 | PSMB2 | GSM4909313 | Human | Breast | IDC | 5.09e-04 | -3.05e-01 | 0.0391 |
5690 | PSMB2 | GSM4909315 | Human | Breast | IDC | 1.15e-02 | 2.69e-01 | 0.21 |
5690 | PSMB2 | GSM4909316 | Human | Breast | IDC | 1.62e-06 | 4.24e-01 | 0.21 |
5690 | PSMB2 | GSM4909319 | Human | Breast | IDC | 9.72e-31 | -3.65e-01 | 0.1563 |
5690 | PSMB2 | GSM4909320 | Human | Breast | IDC | 2.91e-05 | -2.49e-01 | 0.1575 |
5690 | PSMB2 | GSM4909321 | Human | Breast | IDC | 2.40e-13 | -8.43e-02 | 0.1559 |
5690 | PSMB2 | brca1 | Human | Breast | Precancer | 2.37e-39 | 7.00e-01 | -0.0338 |
5690 | PSMB2 | brca2 | Human | Breast | Precancer | 1.68e-19 | 5.42e-01 | -0.024 |
5690 | PSMB2 | brca3 | Human | Breast | Precancer | 4.30e-07 | 3.47e-01 | -0.0263 |
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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:00104989 | Breast | Precancer | proteasomal protein catabolic process | 58/1080 | 490/18723 | 1.54e-07 | 8.05e-06 | 58 |
GO:001049814 | Breast | IDC | proteasomal protein catabolic process | 75/1434 | 490/18723 | 5.59e-09 | 4.41e-07 | 75 |
GO:001049824 | Breast | DCIS | proteasomal protein catabolic process | 75/1390 | 490/18723 | 1.44e-09 | 1.40e-07 | 75 |
GO:0010498 | Colorectum | AD | proteasomal protein catabolic process | 174/3918 | 490/18723 | 3.18e-14 | 7.66e-12 | 174 |
GO:00104982 | Colorectum | MSS | proteasomal protein catabolic process | 157/3467 | 490/18723 | 2.39e-13 | 5.25e-11 | 157 |
GO:00104983 | Colorectum | MSI-H | proteasomal protein catabolic process | 71/1319 | 490/18723 | 4.67e-09 | 6.03e-07 | 71 |
GO:00104984 | Colorectum | FAP | proteasomal protein catabolic process | 110/2622 | 490/18723 | 2.12e-07 | 1.26e-05 | 110 |
GO:001049816 | Endometrium | AEH | proteasomal protein catabolic process | 108/2100 | 490/18723 | 2.73e-12 | 4.67e-10 | 108 |
GO:001049817 | Endometrium | EEC | proteasomal protein catabolic process | 112/2168 | 490/18723 | 6.99e-13 | 1.40e-10 | 112 |
GO:001049826 | Esophagus | HGIN | proteasomal protein catabolic process | 139/2587 | 490/18723 | 1.20e-17 | 3.41e-15 | 139 |
GO:0010498111 | Esophagus | ESCC | proteasomal protein catabolic process | 369/8552 | 490/18723 | 1.13e-41 | 1.80e-38 | 369 |
GO:001049812 | Liver | Cirrhotic | proteasomal protein catabolic process | 216/4634 | 490/18723 | 2.52e-21 | 9.29e-19 | 216 |
GO:001049822 | Liver | HCC | proteasomal protein catabolic process | 351/7958 | 490/18723 | 6.92e-40 | 1.46e-36 | 351 |
GO:001049820 | Oral cavity | OSCC | proteasomal protein catabolic process | 336/7305 | 490/18723 | 5.45e-41 | 8.63e-38 | 336 |
GO:0010498110 | Oral cavity | LP | proteasomal protein catabolic process | 224/4623 | 490/18723 | 9.57e-25 | 4.00e-22 | 224 |
GO:001049828 | Skin | cSCC | proteasomal protein catabolic process | 243/4864 | 490/18723 | 7.85e-30 | 4.10e-27 | 243 |
GO:0010498113 | Thyroid | PTC | proteasomal protein catabolic process | 297/5968 | 490/18723 | 4.58e-40 | 9.63e-37 | 297 |
GO:001049832 | Thyroid | ATC | proteasomal protein catabolic process | 309/6293 | 490/18723 | 1.78e-41 | 1.13e-37 | 309 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa050141 | Colorectum | AD | Amyotrophic lateral sclerosis | 164/2092 | 364/8465 | 4.28e-18 | 1.27e-16 | 8.09e-17 | 164 |
hsa050221 | Colorectum | AD | Pathways of neurodegeneration - multiple diseases | 201/2092 | 476/8465 | 4.54e-18 | 1.27e-16 | 8.09e-17 | 201 |
hsa030501 | Colorectum | AD | Proteasome | 29/2092 | 46/8465 | 3.87e-08 | 6.18e-07 | 3.94e-07 | 29 |
hsa050171 | Colorectum | AD | Spinocerebellar ataxia | 60/2092 | 143/8465 | 3.78e-06 | 4.35e-05 | 2.78e-05 | 60 |
hsa050124 | Colorectum | MSS | Parkinson disease | 140/1875 | 266/8465 | 2.32e-28 | 7.79e-26 | 4.77e-26 | 140 |
hsa050104 | Colorectum | MSS | Alzheimer disease | 169/1875 | 384/8465 | 1.21e-22 | 1.01e-20 | 6.21e-21 | 169 |
hsa050164 | Colorectum | MSS | Huntington disease | 141/1875 | 306/8465 | 2.90e-21 | 1.62e-19 | 9.92e-20 | 141 |
hsa050204 | Colorectum | MSS | Prion disease | 129/1875 | 273/8465 | 1.04e-20 | 5.00e-19 | 3.06e-19 | 129 |
hsa050224 | Colorectum | MSS | Pathways of neurodegeneration - multiple diseases | 192/1875 | 476/8465 | 2.79e-20 | 1.04e-18 | 6.36e-19 | 192 |
hsa050144 | Colorectum | MSS | Amyotrophic lateral sclerosis | 156/1875 | 364/8465 | 1.43e-19 | 4.62e-18 | 2.83e-18 | 156 |
hsa030504 | Colorectum | MSS | Proteasome | 29/1875 | 46/8465 | 2.72e-09 | 5.69e-08 | 3.48e-08 | 29 |
hsa050174 | Colorectum | MSS | Spinocerebellar ataxia | 60/1875 | 143/8465 | 7.14e-08 | 1.26e-06 | 7.71e-07 | 60 |
hsa050125 | Colorectum | MSS | Parkinson disease | 140/1875 | 266/8465 | 2.32e-28 | 7.79e-26 | 4.77e-26 | 140 |
hsa050105 | Colorectum | MSS | Alzheimer disease | 169/1875 | 384/8465 | 1.21e-22 | 1.01e-20 | 6.21e-21 | 169 |
hsa050165 | Colorectum | MSS | Huntington disease | 141/1875 | 306/8465 | 2.90e-21 | 1.62e-19 | 9.92e-20 | 141 |
hsa050205 | Colorectum | MSS | Prion disease | 129/1875 | 273/8465 | 1.04e-20 | 5.00e-19 | 3.06e-19 | 129 |
hsa050225 | Colorectum | MSS | Pathways of neurodegeneration - multiple diseases | 192/1875 | 476/8465 | 2.79e-20 | 1.04e-18 | 6.36e-19 | 192 |
hsa050145 | Colorectum | MSS | Amyotrophic lateral sclerosis | 156/1875 | 364/8465 | 1.43e-19 | 4.62e-18 | 2.83e-18 | 156 |
hsa030505 | Colorectum | MSS | Proteasome | 29/1875 | 46/8465 | 2.72e-09 | 5.69e-08 | 3.48e-08 | 29 |
hsa050175 | Colorectum | MSS | Spinocerebellar ataxia | 60/1875 | 143/8465 | 7.14e-08 | 1.26e-06 | 7.71e-07 | 60 |
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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 |
PSMB2 | SNV | Missense_Mutation | novel | c.338C>A | p.Pro113Gln | p.P113Q | P49721 | protein_coding | deleterious(0) | probably_damaging(0.926) | TCGA-A2-A25A-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unspecific | Cytoxan | SD |
PSMB2 | insertion | Frame_Shift_Ins | novel | c.16_17insATGAG | p.Gly6AspfsTer25 | p.G6Dfs*25 | P49721 | protein_coding | TCGA-A7-A0CE-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | ||
PSMB2 | SNV | Missense_Mutation | c.10N>T | p.Leu4Phe | p.L4F | P49721 | protein_coding | deleterious(0.02) | probably_damaging(0.975) | TCGA-EK-A2RC-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
PSMB2 | SNV | Missense_Mutation | novel | c.413N>C | p.Leu138Pro | p.L138P | P49721 | protein_coding | deleterious(0) | probably_damaging(0.946) | TCGA-AA-3947-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
PSMB2 | SNV | Missense_Mutation | novel | c.284G>T | p.Arg95Leu | p.R95L | P49721 | protein_coding | deleterious(0) | benign(0.06) | TCGA-AA-3949-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
PSMB2 | SNV | Missense_Mutation | rs774332216 | c.209N>A | p.Arg70Gln | p.R70Q | P49721 | protein_coding | deleterious(0) | benign(0.387) | TCGA-EI-6917-01 | Colorectum | rectum adenocarcinoma | Male | <65 | III/IV | Chemotherapy | 5fluorouracil+oxaciplatina+l-folinian | SD |
PSMB2 | SNV | Missense_Mutation | novel | c.68N>T | p.Ser23Ile | p.S23I | P49721 | protein_coding | deleterious(0.03) | benign(0.224) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
PSMB2 | SNV | Missense_Mutation | rs775992910 | c.542N>A | p.Arg181Gln | p.R181Q | P49721 | protein_coding | tolerated(0.42) | benign(0.232) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
PSMB2 | SNV | Missense_Mutation | novel | c.373G>A | p.Ala125Thr | p.A125T | P49721 | protein_coding | tolerated(0.22) | possibly_damaging(0.545) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
PSMB2 | SNV | Missense_Mutation | novel | c.70N>G | p.Asn24Asp | p.N24D | P49721 | protein_coding | deleterious(0.03) | benign(0) | TCGA-AX-A2HJ-01 | Endometrium | uterine corpus endometrioid carcinoma | 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 |
5690 | PSMB2 | DRUGGABLE GENOME, PROTEASE, ENZYME | inhibitor | CHEMBL451887 | CARFILZOMIB | |
5690 | PSMB2 | DRUGGABLE GENOME, PROTEASE, ENZYME | inhibitor | CHEMBL371405 | MARIZOMIB | |
5690 | PSMB2 | DRUGGABLE GENOME, PROTEASE, ENZYME | MLN-9708 | IXAZOMIB CITRATE | ||
5690 | PSMB2 | DRUGGABLE GENOME, PROTEASE, ENZYME | CARFILZOMIB | CARFILZOMIB | ||
5690 | PSMB2 | DRUGGABLE GENOME, PROTEASE, ENZYME | inhibitor | 385612170 | KZR-616 | |
5690 | PSMB2 | DRUGGABLE GENOME, PROTEASE, ENZYME | CARFILZOMIB | CARFILZOMIB | 24524217 | |
5690 | PSMB2 | DRUGGABLE GENOME, PROTEASE, ENZYME | BORTEZOMIB | BORTEZOMIB | 24524217 | |
5690 | PSMB2 | DRUGGABLE GENOME, PROTEASE, ENZYME | MG-132 | MG-132 | 24321833 | |
5690 | PSMB2 | DRUGGABLE GENOME, PROTEASE, ENZYME | inhibitor | CARFILZOMIB | CARFILZOMIB | |
5690 | PSMB2 | DRUGGABLE GENOME, PROTEASE, ENZYME | OPROZOMIB | OPROZOMIB |
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