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Gene: MSX1 |
Gene summary for MSX1 |
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Gene information | Species | Human | Gene symbol | MSX1 | Gene ID | 4487 |
Gene name | msh homeobox 1 | |
Gene Alias | ECTD3 | |
Cytomap | 4p16.2 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | P28360 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
4487 | MSX1 | AEH-subject3 | Human | Endometrium | AEH | 1.20e-09 | 4.70e-01 | -0.2576 |
4487 | MSX1 | EEC-subject3 | Human | Endometrium | EEC | 5.34e-05 | -1.56e-01 | -0.2525 |
4487 | MSX1 | EEC-subject5 | Human | Endometrium | EEC | 8.71e-06 | 3.82e-01 | -0.249 |
4487 | MSX1 | GSM5276934 | Human | Endometrium | EEC | 3.70e-23 | -6.98e-01 | -0.0913 |
4487 | MSX1 | GSM5276935 | Human | Endometrium | EEC | 2.29e-47 | 8.68e-01 | -0.123 |
4487 | MSX1 | GSM6177620_NYU_UCEC1_lib1_lib1 | Human | Endometrium | EEC | 5.43e-19 | 3.70e-01 | -0.1869 |
4487 | MSX1 | GSM6177620_NYU_UCEC1_lib2_lib2 | Human | Endometrium | EEC | 1.83e-07 | 5.47e-02 | -0.1875 |
4487 | MSX1 | GSM6177620_NYU_UCEC1_lib3_lib3 | Human | Endometrium | EEC | 3.61e-18 | 2.96e-01 | -0.1883 |
4487 | MSX1 | GSM6177621_NYU_UCEC2_lib1_lib1 | Human | Endometrium | EEC | 7.32e-39 | 7.89e-01 | -0.1934 |
4487 | MSX1 | GSM6177622_NYU_UCEC3_lib1_lib1 | Human | Endometrium | EEC | 1.13e-14 | -3.61e-02 | -0.1917 |
4487 | MSX1 | GSM6177622_NYU_UCEC3_lib2_lib2 | Human | Endometrium | EEC | 7.91e-14 | -3.32e-02 | -0.1916 |
4487 | MSX1 | HCC2_Meng | Human | Liver | HCC | 4.33e-03 | 5.24e-02 | 0.0107 |
4487 | MSX1 | HCC1 | Human | Liver | HCC | 1.89e-02 | 1.26e+00 | 0.5336 |
4487 | MSX1 | HCC2 | Human | Liver | HCC | 5.93e-12 | 1.40e+00 | 0.5341 |
4487 | MSX1 | HCC5 | Human | Liver | HCC | 1.75e-08 | 3.33e-01 | 0.4932 |
4487 | MSX1 | S014 | Human | Liver | HCC | 5.98e-30 | 1.31e+00 | 0.2254 |
4487 | MSX1 | S015 | Human | Liver | HCC | 9.34e-34 | 1.42e+00 | 0.2375 |
4487 | MSX1 | S016 | Human | Liver | HCC | 1.48e-31 | 1.15e+00 | 0.2243 |
4487 | MSX1 | S027 | Human | Liver | HCC | 9.18e-07 | 3.32e-01 | 0.2446 |
4487 | MSX1 | S028 | Human | Liver | HCC | 8.36e-16 | 4.02e-01 | 0.2503 |
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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 |
Esophagus | ESCC | ![]() |
Skin | AK | ![]() |
Skin | SCCIS | ![]() |
Skin | cSCC | ![]() |
Thyroid | HT | ![]() |
∗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:003164716 | Endometrium | AEH | regulation of protein stability | 77/2100 | 298/18723 | 1.13e-12 | 2.26e-10 | 77 |
GO:009719316 | Endometrium | AEH | intrinsic apoptotic signaling pathway | 75/2100 | 288/18723 | 1.46e-12 | 2.83e-10 | 75 |
GO:200123316 | Endometrium | AEH | regulation of apoptotic signaling pathway | 86/2100 | 356/18723 | 2.97e-12 | 4.95e-10 | 86 |
GO:005082116 | Endometrium | AEH | protein stabilization | 55/2100 | 191/18723 | 2.19e-11 | 3.20e-09 | 55 |
GO:200124216 | Endometrium | AEH | regulation of intrinsic apoptotic signaling pathway | 49/2100 | 164/18723 | 6.39e-11 | 8.16e-09 | 49 |
GO:005109816 | Endometrium | AEH | regulation of binding | 77/2100 | 363/18723 | 2.21e-08 | 1.31e-06 | 77 |
GO:00605376 | Endometrium | AEH | muscle tissue development | 83/2100 | 403/18723 | 2.57e-08 | 1.50e-06 | 83 |
GO:20012358 | Endometrium | AEH | positive regulation of apoptotic signaling pathway | 36/2100 | 126/18723 | 7.56e-08 | 3.92e-06 | 36 |
GO:00160499 | Endometrium | AEH | cell growth | 93/2100 | 482/18723 | 1.00e-07 | 4.99e-06 | 93 |
GO:20012447 | Endometrium | AEH | positive regulation of intrinsic apoptotic signaling pathway | 21/2100 | 58/18723 | 5.46e-07 | 2.10e-05 | 21 |
GO:00017019 | Endometrium | AEH | in utero embryonic development | 73/2100 | 367/18723 | 7.18e-07 | 2.63e-05 | 73 |
GO:19022539 | Endometrium | AEH | regulation of intrinsic apoptotic signaling pathway by p53 class mediator | 14/2100 | 29/18723 | 7.20e-07 | 2.63e-05 | 14 |
GO:004873216 | Endometrium | AEH | gland development | 83/2100 | 436/18723 | 8.62e-07 | 3.11e-05 | 83 |
GO:00147065 | Endometrium | AEH | striated muscle tissue development | 75/2100 | 384/18723 | 1.06e-06 | 3.62e-05 | 75 |
GO:007233210 | Endometrium | AEH | intrinsic apoptotic signaling pathway by p53 class mediator | 24/2100 | 76/18723 | 1.54e-06 | 4.85e-05 | 24 |
GO:00071787 | Endometrium | AEH | transmembrane receptor protein serine/threonine kinase signaling pathway | 67/2100 | 355/18723 | 1.28e-05 | 2.80e-04 | 67 |
GO:00345049 | Endometrium | AEH | protein localization to nucleus | 57/2100 | 290/18723 | 1.65e-05 | 3.42e-04 | 57 |
GO:00015589 | Endometrium | AEH | regulation of cell growth | 75/2100 | 414/18723 | 1.79e-05 | 3.65e-04 | 75 |
GO:190179816 | Endometrium | AEH | positive regulation of signal transduction by p53 class mediator | 11/2100 | 25/18723 | 3.42e-05 | 6.06e-04 | 11 |
GO:007233116 | Endometrium | AEH | signal transduction by p53 class mediator | 36/2100 | 163/18723 | 4.88e-05 | 7.95e-04 | 36 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0516626 | Endometrium | AEH | Human T-cell leukemia virus 1 infection | 50/1197 | 222/8465 | 4.30e-04 | 3.11e-03 | 2.27e-03 | 50 |
hsa05166111 | Endometrium | AEH | Human T-cell leukemia virus 1 infection | 50/1197 | 222/8465 | 4.30e-04 | 3.11e-03 | 2.27e-03 | 50 |
hsa0516627 | Endometrium | EEC | Human T-cell leukemia virus 1 infection | 52/1237 | 222/8465 | 2.73e-04 | 2.36e-03 | 1.76e-03 | 52 |
hsa0516636 | Endometrium | EEC | Human T-cell leukemia virus 1 infection | 52/1237 | 222/8465 | 2.73e-04 | 2.36e-03 | 1.76e-03 | 52 |
hsa0516622 | Liver | HCC | Human T-cell leukemia virus 1 infection | 139/4020 | 222/8465 | 3.17e-06 | 2.79e-05 | 1.55e-05 | 139 |
hsa0516632 | Liver | HCC | Human T-cell leukemia virus 1 infection | 139/4020 | 222/8465 | 3.17e-06 | 2.79e-05 | 1.55e-05 | 139 |
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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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∗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 |
MSX1 | SNV | Missense_Mutation | c.527N>A | p.Arg176Gln | p.R176Q | P28360 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A7-A2KD-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cytoxan | SD | |
MSX1 | SNV | Missense_Mutation | c.566N>A | p.Arg189His | p.R189H | P28360 | protein_coding | deleterious(0) | probably_damaging(0.986) | TCGA-IR-A3LI-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
MSX1 | SNV | Missense_Mutation | c.893G>A | p.Ser298Asn | p.S298N | P28360 | protein_coding | tolerated(0.06) | possibly_damaging(0.749) | TCGA-A6-5665-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
MSX1 | SNV | Missense_Mutation | novel | c.436N>G | p.Met146Val | p.M146V | P28360 | protein_coding | tolerated(0.55) | benign(0.047) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR |
MSX1 | SNV | Missense_Mutation | c.809C>T | p.Ser270Leu | p.S270L | P28360 | protein_coding | tolerated(0.07) | benign(0.445) | TCGA-AM-5821-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MSX1 | SNV | Missense_Mutation | c.253G>A | p.Gly85Ser | p.G85S | P28360 | protein_coding | tolerated(0.36) | benign(0.029) | TCGA-AY-A69D-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
MSX1 | SNV | Missense_Mutation | c.722N>A | p.Ala241Asp | p.A241D | P28360 | protein_coding | deleterious(0) | probably_damaging(0.974) | TCGA-G4-6302-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MSX1 | SNV | Missense_Mutation | c.574N>T | p.Arg192Cys | p.R192C | P28360 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-WS-AB45-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
MSX1 | SNV | Missense_Mutation | c.623C>T | p.Ser208Leu | p.S208L | P28360 | protein_coding | deleterious(0) | probably_damaging(0.992) | TCGA-A5-A0G9-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MSX1 | SNV | Missense_Mutation | novel | c.589N>A | p.Leu197Met | p.L197M | P28360 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A5-A1OF-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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