![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: SMYD2 |
Gene summary for SMYD2 |
![]() |
Gene information | Species | Human | Gene symbol | SMYD2 | Gene ID | 56950 |
Gene name | SET and MYND domain containing 2 | |
Gene Alias | HSKM-B | |
Cytomap | 1q32.3 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | Q9NRG4 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
56950 | SMYD2 | LZE4T | Human | Esophagus | ESCC | 5.89e-10 | 1.83e-01 | 0.0811 |
56950 | SMYD2 | LZE7T | Human | Esophagus | ESCC | 5.24e-07 | 4.38e-01 | 0.0667 |
56950 | SMYD2 | LZE8T | Human | Esophagus | ESCC | 1.22e-03 | 4.70e-02 | 0.067 |
56950 | SMYD2 | LZE20T | Human | Esophagus | ESCC | 1.61e-03 | 6.70e-02 | 0.0662 |
56950 | SMYD2 | LZE22D1 | Human | Esophagus | HGIN | 3.06e-03 | 2.12e-01 | 0.0595 |
56950 | SMYD2 | LZE24T | Human | Esophagus | ESCC | 1.67e-14 | 5.26e-01 | 0.0596 |
56950 | SMYD2 | LZE22D3 | Human | Esophagus | HGIN | 2.35e-03 | 3.43e-01 | 0.0653 |
56950 | SMYD2 | LZE6T | Human | Esophagus | ESCC | 1.24e-06 | 1.38e-01 | 0.0845 |
56950 | SMYD2 | P1T-E | Human | Esophagus | ESCC | 7.64e-06 | 3.01e-01 | 0.0875 |
56950 | SMYD2 | P2T-E | Human | Esophagus | ESCC | 9.99e-20 | 4.69e-01 | 0.1177 |
56950 | SMYD2 | P4T-E | Human | Esophagus | ESCC | 6.93e-22 | 5.03e-01 | 0.1323 |
56950 | SMYD2 | P5T-E | Human | Esophagus | ESCC | 1.28e-15 | 4.05e-01 | 0.1327 |
56950 | SMYD2 | P8T-E | Human | Esophagus | ESCC | 1.17e-15 | 2.39e-01 | 0.0889 |
56950 | SMYD2 | P9T-E | Human | Esophagus | ESCC | 1.26e-15 | 3.16e-01 | 0.1131 |
56950 | SMYD2 | P10T-E | Human | Esophagus | ESCC | 1.93e-26 | 6.00e-01 | 0.116 |
56950 | SMYD2 | P11T-E | Human | Esophagus | ESCC | 1.54e-09 | 4.17e-01 | 0.1426 |
56950 | SMYD2 | P12T-E | Human | Esophagus | ESCC | 6.59e-17 | 3.42e-01 | 0.1122 |
56950 | SMYD2 | P15T-E | Human | Esophagus | ESCC | 2.87e-33 | 7.00e-01 | 0.1149 |
56950 | SMYD2 | P16T-E | Human | Esophagus | ESCC | 1.05e-10 | 3.26e-01 | 0.1153 |
56950 | SMYD2 | P17T-E | Human | Esophagus | ESCC | 4.63e-09 | 4.37e-01 | 0.1278 |
Page: 1 2 3 4 5 6 |
![]() |
∗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. |
Top |
Malignant transformation related pathway analysis |
![]() |
![]() |
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 |
![]() |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:007233127 | Esophagus | HGIN | signal transduction by p53 class mediator | 49/2587 | 163/18723 | 5.71e-08 | 3.06e-06 | 49 |
GO:00182057 | Esophagus | HGIN | peptidyl-lysine modification | 88/2587 | 376/18723 | 2.99e-07 | 1.39e-05 | 88 |
GO:003033020 | Esophagus | HGIN | DNA damage response, signal transduction by p53 class mediator | 24/2587 | 72/18723 | 2.03e-05 | 5.43e-04 | 24 |
GO:200102019 | Esophagus | HGIN | regulation of response to DNA damage stimulus | 52/2587 | 219/18723 | 5.00e-05 | 1.19e-03 | 52 |
GO:00165708 | Esophagus | HGIN | histone modification | 92/2587 | 463/18723 | 1.70e-04 | 3.30e-03 | 92 |
GO:190179627 | Esophagus | HGIN | regulation of signal transduction by p53 class mediator | 26/2587 | 93/18723 | 2.60e-04 | 4.55e-03 | 26 |
GO:00427708 | Esophagus | HGIN | signal transduction in response to DNA damage | 39/2587 | 172/18723 | 1.07e-03 | 1.32e-02 | 39 |
GO:0018027 | Esophagus | HGIN | peptidyl-lysine dimethylation | 10/2587 | 26/18723 | 1.60e-03 | 1.79e-02 | 10 |
GO:00349688 | Esophagus | HGIN | histone lysine methylation | 27/2587 | 115/18723 | 3.51e-03 | 3.24e-02 | 27 |
GO:00435168 | Esophagus | HGIN | regulation of DNA damage response, signal transduction by p53 class mediator | 11/2587 | 34/18723 | 4.61e-03 | 3.96e-02 | 11 |
GO:00064798 | Esophagus | HGIN | protein methylation | 38/2587 | 181/18723 | 5.05e-03 | 4.22e-02 | 38 |
GO:00082138 | Esophagus | HGIN | protein alkylation | 38/2587 | 181/18723 | 5.05e-03 | 4.22e-02 | 38 |
GO:00180227 | Esophagus | HGIN | peptidyl-lysine methylation | 29/2587 | 131/18723 | 6.22e-03 | 4.95e-02 | 29 |
GO:001657015 | Esophagus | ESCC | histone modification | 323/8552 | 463/18723 | 2.61e-26 | 7.88e-24 | 323 |
GO:001820514 | Esophagus | ESCC | peptidyl-lysine modification | 259/8552 | 376/18723 | 3.90e-20 | 5.26e-18 | 259 |
GO:0072331111 | Esophagus | ESCC | signal transduction by p53 class mediator | 121/8552 | 163/18723 | 9.61e-14 | 4.69e-12 | 121 |
GO:00434143 | Esophagus | ESCC | macromolecule methylation | 199/8552 | 316/18723 | 3.44e-10 | 9.57e-09 | 199 |
GO:2001020110 | Esophagus | ESCC | regulation of response to DNA damage stimulus | 145/8552 | 219/18723 | 5.97e-10 | 1.50e-08 | 145 |
GO:00322592 | Esophagus | ESCC | methylation | 222/8552 | 364/18723 | 2.26e-09 | 5.09e-08 | 222 |
GO:004277014 | Esophagus | ESCC | signal transduction in response to DNA damage | 117/8552 | 172/18723 | 2.38e-09 | 5.32e-08 | 117 |
Page: 1 2 3 4 5 |
![]() |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0031010 | Esophagus | ESCC | Lysine degradation | 41/4205 | 63/8465 | 9.63e-03 | 2.27e-02 | 1.16e-02 | 41 |
hsa0031013 | Esophagus | ESCC | Lysine degradation | 41/4205 | 63/8465 | 9.63e-03 | 2.27e-02 | 1.16e-02 | 41 |
hsa0031021 | Liver | Cirrhotic | Lysine degradation | 29/2530 | 63/8465 | 4.81e-03 | 1.74e-02 | 1.07e-02 | 29 |
hsa0031031 | Liver | Cirrhotic | Lysine degradation | 29/2530 | 63/8465 | 4.81e-03 | 1.74e-02 | 1.07e-02 | 29 |
hsa0031041 | Liver | HCC | Lysine degradation | 47/4020 | 63/8465 | 1.02e-05 | 7.58e-05 | 4.22e-05 | 47 |
hsa0031051 | Liver | HCC | Lysine degradation | 47/4020 | 63/8465 | 1.02e-05 | 7.58e-05 | 4.22e-05 | 47 |
Page: 1 |
Top |
Cell-cell communication analysis |
![]() |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
Top |
Single-cell gene regulatory network inference analysis |
![]() |
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 |
Top |
Somatic mutation of malignant transformation related genes |
![]() |
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 |
SMYD2 | SNV | Missense_Mutation | novel | c.766G>A | p.Asp256Asn | p.D256N | Q9NRG4 | protein_coding | tolerated(0.09) | possibly_damaging(0.798) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
SMYD2 | SNV | Missense_Mutation | c.559G>A | p.Glu187Lys | p.E187K | Q9NRG4 | protein_coding | tolerated(0.12) | probably_damaging(0.998) | TCGA-D8-A1JJ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicine | SD | |
SMYD2 | insertion | Nonsense_Mutation | novel | c.588_589insGAGTCAGAAGCTGTCTGTCCCTAGATCAGTTTTGAAAAGTGTT | p.Ala197GlufsTer8 | p.A197Efs*8 | Q9NRG4 | protein_coding | TCGA-A8-A09D-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | CR | ||
SMYD2 | SNV | Missense_Mutation | novel | c.409C>T | p.His137Tyr | p.H137Y | Q9NRG4 | protein_coding | deleterious(0) | probably_damaging(0.986) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
SMYD2 | SNV | Missense_Mutation | rs369877948 | c.517N>A | p.Val173Ile | p.V173I | Q9NRG4 | protein_coding | tolerated(0.28) | benign(0.001) | TCGA-CK-6746-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
SMYD2 | deletion | Frame_Shift_Del | c.67delG | p.Ala23LeufsTer84 | p.A23Lfs*84 | Q9NRG4 | protein_coding | TCGA-CM-5861-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | PD | |||
SMYD2 | insertion | Frame_Shift_Ins | novel | c.283_284insT | p.Gly97TrpfsTer39 | p.G97Wfs*39 | Q9NRG4 | protein_coding | TCGA-G4-6320-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | oxaliplatin | SD | ||
SMYD2 | SNV | Missense_Mutation | rs372313690 | c.740C>T | p.Thr247Met | p.T247M | Q9NRG4 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
SMYD2 | SNV | Missense_Mutation | rs369082796 | c.493G>A | p.Gly165Arg | p.G165R | Q9NRG4 | protein_coding | tolerated(0.19) | benign(0.038) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
SMYD2 | SNV | Missense_Mutation | c.378A>T | p.Glu126Asp | p.E126D | Q9NRG4 | protein_coding | deleterious(0.01) | possibly_damaging(0.872) | TCGA-AP-A056-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
Page: 1 2 3 4 |
Top |
Related drugs of malignant transformation related genes |
![]() |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
56950 | SMYD2 | ENZYME, METHYL TRANSFERASE | inhibitor | 178103600 | ||
56950 | SMYD2 | ENZYME, METHYL TRANSFERASE | inhibitor | 249565919 | ||
56950 | SMYD2 | ENZYME, METHYL TRANSFERASE | inhibitor | 310264734 |
Page: 1 |