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Gene: MYL6B |
Gene summary for MYL6B |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | MYL6B | Gene ID | 140465 |
| Gene name | myosin light chain 6B | |
| Gene Alias | MLC1SA | |
| Cytomap | 12q13.2 | |
| Gene Type | protein-coding | GO ID | GO:0003008 | UniProtAcc | A0A024RB31 |
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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 |
| 140465 | MYL6B | LZE7T | Human | Esophagus | ESCC | 2.27e-08 | 7.72e-01 | 0.0667 |
| 140465 | MYL6B | LZE8T | Human | Esophagus | ESCC | 5.70e-06 | 2.55e-01 | 0.067 |
| 140465 | MYL6B | LZE20T | Human | Esophagus | ESCC | 1.07e-02 | 8.50e-02 | 0.0662 |
| 140465 | MYL6B | LZE22D1 | Human | Esophagus | HGIN | 1.42e-03 | 3.56e-01 | 0.0595 |
| 140465 | MYL6B | LZE22T | Human | Esophagus | ESCC | 3.16e-05 | 4.01e-01 | 0.068 |
| 140465 | MYL6B | LZE24T | Human | Esophagus | ESCC | 2.01e-11 | 5.21e-01 | 0.0596 |
| 140465 | MYL6B | P1T-E | Human | Esophagus | ESCC | 1.24e-13 | 9.78e-01 | 0.0875 |
| 140465 | MYL6B | P2T-E | Human | Esophagus | ESCC | 5.10e-74 | 1.65e+00 | 0.1177 |
| 140465 | MYL6B | P4T-E | Human | Esophagus | ESCC | 4.65e-44 | 1.07e+00 | 0.1323 |
| 140465 | MYL6B | P5T-E | Human | Esophagus | ESCC | 2.63e-31 | 6.85e-01 | 0.1327 |
| 140465 | MYL6B | P8T-E | Human | Esophagus | ESCC | 1.18e-29 | 5.97e-01 | 0.0889 |
| 140465 | MYL6B | P9T-E | Human | Esophagus | ESCC | 1.28e-20 | 5.14e-01 | 0.1131 |
| 140465 | MYL6B | P10T-E | Human | Esophagus | ESCC | 8.09e-68 | 1.19e+00 | 0.116 |
| 140465 | MYL6B | P11T-E | Human | Esophagus | ESCC | 1.00e-11 | 7.50e-01 | 0.1426 |
| 140465 | MYL6B | P12T-E | Human | Esophagus | ESCC | 5.85e-54 | 1.23e+00 | 0.1122 |
| 140465 | MYL6B | P15T-E | Human | Esophagus | ESCC | 1.80e-29 | 6.94e-01 | 0.1149 |
| 140465 | MYL6B | P16T-E | Human | Esophagus | ESCC | 2.97e-50 | 1.03e+00 | 0.1153 |
| 140465 | MYL6B | P17T-E | Human | Esophagus | ESCC | 8.34e-17 | 6.88e-01 | 0.1278 |
| 140465 | MYL6B | P19T-E | Human | Esophagus | ESCC | 2.76e-11 | 1.21e+00 | 0.1662 |
| 140465 | MYL6B | P20T-E | Human | Esophagus | ESCC | 7.98e-29 | 7.18e-01 | 0.1124 |
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| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Endometrium |  | AEH: Atypical endometrial hyperplasia |
| EEC: Endometrioid Cancer | ||
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| Liver |  | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease | ||
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia | ||
| NEOLP: Non-erosive oral lichen planus | ||
| OSCC: Oral squamous cell carcinoma | ||
| Skin |  | AK: Actinic keratosis |
| cSCC: Cutaneous squamous cell carcinoma | ||
| SCCIS:squamous cell carcinoma in situ | ||
| Thyroid |  | ATC: Anaplastic thyroid cancer |
| HT: Hashimoto's thyroiditis | ||
| PTC: Papillary thyroid cancer |
| ∗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). |
| Page: 1 2 3 4 5 6 7 8 9 |
| Enriched GO biological processes. |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| GO:00605376 | Endometrium | AEH | muscle tissue development | 83/2100 | 403/18723 | 2.57e-08 | 1.50e-06 | 83 |
| GO:00147065 | Endometrium | AEH | striated muscle tissue development | 75/2100 | 384/18723 | 1.06e-06 | 3.62e-05 | 75 |
| GO:00300488 | Endometrium | AEH | actin filament-based movement | 31/2100 | 127/18723 | 2.10e-05 | 4.14e-04 | 31 |
| GO:00030126 | Endometrium | AEH | muscle system process | 78/2100 | 452/18723 | 6.89e-05 | 1.06e-03 | 78 |
| GO:00075174 | Endometrium | AEH | muscle organ development | 60/2100 | 327/18723 | 8.19e-05 | 1.22e-03 | 60 |
| GO:0006936 | Endometrium | AEH | muscle contraction | 59/2100 | 347/18723 | 7.32e-04 | 6.99e-03 | 59 |
| GO:00702524 | Endometrium | AEH | actin-mediated cell contraction | 20/2100 | 97/18723 | 5.00e-03 | 3.14e-02 | 20 |
| GO:00605382 | Endometrium | AEH | skeletal muscle organ development | 30/2100 | 166/18723 | 5.64e-03 | 3.46e-02 | 30 |
| GO:00075193 | Endometrium | AEH | skeletal muscle tissue development | 28/2100 | 155/18723 | 7.35e-03 | 4.19e-02 | 28 |
| GO:006053713 | Endometrium | EEC | muscle tissue development | 82/2168 | 403/18723 | 2.14e-07 | 9.38e-06 | 82 |
| GO:001470612 | Endometrium | EEC | striated muscle tissue development | 74/2168 | 384/18723 | 6.64e-06 | 1.57e-04 | 74 |
| GO:003004814 | Endometrium | EEC | actin filament-based movement | 31/2168 | 127/18723 | 3.90e-05 | 6.56e-04 | 31 |
| GO:000301213 | Endometrium | EEC | muscle system process | 79/2168 | 452/18723 | 1.16e-04 | 1.55e-03 | 79 |
| GO:000751712 | Endometrium | EEC | muscle organ development | 59/2168 | 327/18723 | 3.49e-04 | 3.85e-03 | 59 |
| GO:00069361 | Endometrium | EEC | muscle contraction | 59/2168 | 347/18723 | 1.57e-03 | 1.26e-02 | 59 |
| GO:007025212 | Endometrium | EEC | actin-mediated cell contraction | 20/2168 | 97/18723 | 7.11e-03 | 4.07e-02 | 20 |
| GO:006053811 | Endometrium | EEC | skeletal muscle organ development | 30/2168 | 166/18723 | 8.78e-03 | 4.74e-02 | 30 |
| GO:00605379 | Esophagus | HGIN | muscle tissue development | 76/2587 | 403/18723 | 2.67e-03 | 2.63e-02 | 76 |
| GO:00147068 | Esophagus | HGIN | striated muscle tissue development | 72/2587 | 384/18723 | 3.94e-03 | 3.56e-02 | 72 |
| GO:006053716 | Esophagus | ESCC | muscle tissue development | 211/8552 | 403/18723 | 3.84e-03 | 1.56e-02 | 211 |
| Page: 1 2 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa0453026 | Endometrium | AEH | Tight junction | 54/1197 | 169/8465 | 1.99e-09 | 3.80e-08 | 2.78e-08 | 54 |
| hsa048144 | Endometrium | AEH | Motor proteins | 42/1197 | 193/8465 | 2.41e-03 | 1.42e-02 | 1.04e-02 | 42 |
| hsa04530112 | Endometrium | AEH | Tight junction | 54/1197 | 169/8465 | 1.99e-09 | 3.80e-08 | 2.78e-08 | 54 |
| hsa0481411 | Endometrium | AEH | Motor proteins | 42/1197 | 193/8465 | 2.41e-03 | 1.42e-02 | 1.04e-02 | 42 |
| hsa0453027 | Endometrium | EEC | Tight junction | 54/1237 | 169/8465 | 6.56e-09 | 1.27e-07 | 9.46e-08 | 54 |
| hsa048142 | Endometrium | EEC | Motor proteins | 42/1237 | 193/8465 | 4.43e-03 | 2.39e-02 | 1.78e-02 | 42 |
| hsa0453036 | Endometrium | EEC | Tight junction | 54/1237 | 169/8465 | 6.56e-09 | 1.27e-07 | 9.46e-08 | 54 |
| hsa048143 | Endometrium | EEC | Motor proteins | 42/1237 | 193/8465 | 4.43e-03 | 2.39e-02 | 1.78e-02 | 42 |
| hsa0453039 | Esophagus | HGIN | Tight junction | 40/1383 | 169/8465 | 8.18e-03 | 4.71e-02 | 3.74e-02 | 40 |
| hsa04530115 | Esophagus | HGIN | Tight junction | 40/1383 | 169/8465 | 8.18e-03 | 4.71e-02 | 3.74e-02 | 40 |
| hsa04530211 | Esophagus | ESCC | Tight junction | 105/4205 | 169/8465 | 6.73e-04 | 2.23e-03 | 1.14e-03 | 105 |
| hsa04530310 | Esophagus | ESCC | Tight junction | 105/4205 | 169/8465 | 6.73e-04 | 2.23e-03 | 1.14e-03 | 105 |
| hsa0453022 | Liver | Cirrhotic | Tight junction | 82/2530 | 169/8465 | 2.14e-07 | 2.85e-06 | 1.76e-06 | 82 |
| hsa0453032 | Liver | Cirrhotic | Tight junction | 82/2530 | 169/8465 | 2.14e-07 | 2.85e-06 | 1.76e-06 | 82 |
| hsa0453042 | Liver | HCC | Tight junction | 110/4020 | 169/8465 | 2.45e-06 | 2.28e-05 | 1.27e-05 | 110 |
| hsa0453052 | Liver | HCC | Tight junction | 110/4020 | 169/8465 | 2.45e-06 | 2.28e-05 | 1.27e-05 | 110 |
| hsa0453030 | Oral cavity | OSCC | Tight junction | 102/3704 | 169/8465 | 8.68e-06 | 3.93e-05 | 2.00e-05 | 102 |
| hsa04530114 | Oral cavity | OSCC | Tight junction | 102/3704 | 169/8465 | 8.68e-06 | 3.93e-05 | 2.00e-05 | 102 |
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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 |
| Page: 1 |
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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. |
| Page: 1 |
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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 |
| MYL6B | SNV | Missense_Mutation | c.152N>T | p.Pro51Leu | p.P51L | P14649 | protein_coding | tolerated(0.05) | probably_damaging(0.923) | TCGA-D8-A1J8-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | nolvadex | SD | |
| MYL6B | SNV | Missense_Mutation | c.508N>G | p.Leu170Val | p.L170V | P14649 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-IR-A3LK-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | PD | |
| MYL6B | SNV | Missense_Mutation | c.397G>A | p.Ala133Thr | p.A133T | P14649 | protein_coding | tolerated(0.73) | benign(0.003) | TCGA-AA-3710-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| MYL6B | SNV | Missense_Mutation | rs779611293 | c.356N>T | p.Ser119Leu | p.S119L | P14649 | protein_coding | tolerated(0.22) | benign(0.001) | TCGA-AA-3811-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD |
| MYL6B | SNV | Missense_Mutation | c.290N>A | p.Gly97Asp | p.G97D | P14649 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-3966-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| MYL6B | SNV | Missense_Mutation | c.346N>A | p.Glu116Lys | p.E116K | P14649 | protein_coding | deleterious(0) | benign(0.445) | TCGA-EI-6882-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
| MYL6B | SNV | Missense_Mutation | novel | c.205N>A | p.Phe69Ile | p.F69I | P14649 | protein_coding | deleterious(0.05) | possibly_damaging(0.59) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| MYL6B | SNV | Missense_Mutation | c.56A>T | p.Lys19Ile | p.K19I | P14649 | protein_coding | deleterious_low_confidence(0.02) | probably_damaging(0.916) | TCGA-AP-A054-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | PD | |
| MYL6B | SNV | Missense_Mutation | c.571N>A | p.Asp191Asn | p.D191N | P14649 | protein_coding | deleterious(0.01) | possibly_damaging(0.459) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD | |
| MYL6B | SNV | Missense_Mutation | novel | c.570G>T | p.Glu190Asp | p.E190D | P14649 | protein_coding | deleterious(0.03) | possibly_damaging(0.713) | TCGA-AX-A2HC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | PD |
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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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