![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: KRT4 |
Gene summary for KRT4 |
![]() |
Gene information | Species | Human | Gene symbol | KRT4 | Gene ID | 3851 |
Gene name | keratin 4 | |
Gene Alias | CK-4 | |
Cytomap | 12q13.13 | |
Gene Type | protein-coding | GO ID | GO:0006996 | UniProtAcc | B4DRS2 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
3851 | KRT4 | LZE2T | Human | Esophagus | ESCC | 4.73e-03 | 9.77e-01 | 0.082 |
3851 | KRT4 | LZE5T | Human | Esophagus | ESCC | 9.25e-35 | 3.23e+00 | 0.0514 |
3851 | KRT4 | LZE20T | Human | Esophagus | ESCC | 8.74e-18 | 2.42e+00 | 0.0662 |
3851 | KRT4 | LZE22D1 | Human | Esophagus | HGIN | 1.03e-15 | 9.44e-01 | 0.0595 |
3851 | KRT4 | LZE22T | Human | Esophagus | ESCC | 1.00e-09 | 1.47e+00 | 0.068 |
3851 | KRT4 | LZE24T | Human | Esophagus | ESCC | 8.20e-87 | 5.41e+00 | 0.0596 |
3851 | KRT4 | P8T-E | Human | Esophagus | ESCC | 4.41e-92 | 3.25e+00 | 0.0889 |
3851 | KRT4 | P15T-E | Human | Esophagus | ESCC | 5.26e-03 | 8.67e-01 | 0.1149 |
3851 | KRT4 | P23T-E | Human | Esophagus | ESCC | 1.14e-03 | 4.14e-01 | 0.108 |
3851 | KRT4 | P27T-E | Human | Esophagus | ESCC | 1.41e-02 | 1.75e-01 | 0.1055 |
3851 | KRT4 | P30T-E | Human | Esophagus | ESCC | 6.12e-09 | 9.05e-01 | 0.137 |
3851 | KRT4 | P31T-E | Human | Esophagus | ESCC | 1.08e-16 | 5.77e-01 | 0.1251 |
3851 | KRT4 | P54T-E | Human | Esophagus | ESCC | 2.11e-02 | 1.27e+00 | 0.0975 |
3851 | KRT4 | P62T-E | Human | Esophagus | ESCC | 5.56e-05 | 8.79e-01 | 0.1302 |
3851 | KRT4 | P65T-E | Human | Esophagus | ESCC | 6.37e-57 | 2.72e+00 | 0.0978 |
3851 | KRT4 | P74T-E | Human | Esophagus | ESCC | 1.20e-14 | 2.51e+00 | 0.1479 |
3851 | KRT4 | P75T-E | Human | Esophagus | ESCC | 5.39e-46 | 2.35e+00 | 0.1125 |
3851 | KRT4 | P80T-E | Human | Esophagus | ESCC | 4.88e-05 | 1.02e+00 | 0.155 |
3851 | KRT4 | P82T-E | Human | Esophagus | ESCC | 2.98e-07 | 1.21e+00 | 0.1072 |
3851 | KRT4 | P127T-E | Human | Esophagus | ESCC | 3.19e-68 | 2.81e+00 | 0.0826 |
Page: 1 2 |
![]() |
∗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:005067318 | Esophagus | ESCC | epithelial cell proliferation | 238/8552 | 437/18723 | 1.19e-04 | 8.20e-04 | 238 |
GO:005067817 | Esophagus | ESCC | regulation of epithelial cell proliferation | 206/8552 | 381/18723 | 5.51e-04 | 3.02e-03 | 206 |
GO:005067310 | Oral cavity | OSCC | epithelial cell proliferation | 212/7305 | 437/18723 | 2.82e-05 | 2.61e-04 | 212 |
GO:005067810 | Oral cavity | OSCC | regulation of epithelial cell proliferation | 180/7305 | 381/18723 | 5.88e-04 | 3.35e-03 | 180 |
Page: 1 |
![]() |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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 |
KRT4 | SNV | Missense_Mutation | c.854N>A | p.Thr285Asn | p.T285N | P19013 | protein_coding | tolerated(0.1) | benign(0.006) | TCGA-A2-A25B-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | PD | |
KRT4 | SNV | Missense_Mutation | rs377329227 | c.1259N>A | p.Arg420His | p.R420H | P19013 | protein_coding | deleterious(0.01) | benign(0.171) | TCGA-B6-A0I8-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
KRT4 | SNV | Missense_Mutation | rs200953989 | c.658G>A | p.Val220Met | p.V220M | P19013 | protein_coding | deleterious(0) | probably_damaging(0.913) | TCGA-B6-A0RQ-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
KRT4 | SNV | Missense_Mutation | novel | c.701G>T | p.Arg234Leu | p.R234L | P19013 | protein_coding | deleterious(0) | possibly_damaging(0.583) | TCGA-BH-A1F5-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
KRT4 | SNV | Missense_Mutation | rs761182348 | c.56N>T | p.Ser19Leu | p.S19L | P19013 | protein_coding | deleterious(0) | possibly_damaging(0.823) | TCGA-OL-A66L-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
KRT4 | deletion | Frame_Shift_Del | novel | c.981delN | p.Ala328ProfsTer21 | p.A328Pfs*21 | P19013 | protein_coding | TCGA-D8-A27V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
KRT4 | SNV | Missense_Mutation | rs774011441 | c.712N>A | p.Glu238Lys | p.E238K | P19013 | protein_coding | deleterious(0) | probably_damaging(0.979) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
KRT4 | SNV | Missense_Mutation | c.26N>C | p.Arg9Pro | p.R9P | P19013 | protein_coding | deleterious_low_confidence(0.01) | probably_damaging(0.921) | TCGA-EK-A2PG-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
KRT4 | SNV | Missense_Mutation | novel | c.1475N>A | p.Ser492Tyr | p.S492Y | P19013 | protein_coding | tolerated_low_confidence(0.58) | benign(0.336) | TCGA-MY-A913-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
KRT4 | SNV | Missense_Mutation | rs539298697 | c.869C>T | p.Thr290Met | p.T290M | P19013 | protein_coding | tolerated(0.07) | possibly_damaging(0.49) | TCGA-VS-A957-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
Page: 1 2 3 4 5 6 7 8 |
Top |
Related drugs of malignant transformation related genes |
![]() |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
Page: 1 |