|
Gene: ZNF598 |
Gene summary for ZNF598 |
Gene summary. |
Gene information | Species | Human | Gene symbol | ZNF598 | Gene ID | 90850 |
Gene name | zinc finger protein 598, E3 ubiquitin ligase | |
Gene Alias | HEL2 | |
Cytomap | 16p13.3 | |
Gene Type | protein-coding | GO ID | GO:0006412 | UniProtAcc | Q86UK7 |
Top |
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 |
90850 | ZNF598 | SYSMH1 | Human | Oral cavity | OSCC | 1.67e-02 | 1.82e-01 | 0.1127 |
90850 | ZNF598 | SYSMH2 | Human | Oral cavity | OSCC | 3.23e-15 | 4.44e-01 | 0.2326 |
90850 | ZNF598 | SYSMH3 | Human | Oral cavity | OSCC | 2.42e-39 | 8.09e-01 | 0.2442 |
90850 | ZNF598 | SYSMH5 | Human | Oral cavity | OSCC | 4.42e-10 | 3.35e-01 | 0.0647 |
90850 | ZNF598 | SYSMH6 | Human | Oral cavity | OSCC | 1.08e-02 | 1.57e-01 | 0.1275 |
90850 | ZNF598 | P4_S8_cSCC | Human | Skin | cSCC | 2.20e-03 | 1.62e-01 | -0.3095 |
90850 | ZNF598 | P1_cSCC | Human | Skin | cSCC | 7.60e-16 | 6.30e-01 | 0.0292 |
90850 | ZNF598 | P2_cSCC | Human | Skin | cSCC | 4.61e-06 | 2.93e-01 | -0.024 |
90850 | ZNF598 | P4_cSCC | Human | Skin | cSCC | 2.15e-08 | 3.30e-01 | -0.00290000000000005 |
90850 | ZNF598 | P10_cSCC | Human | Skin | cSCC | 1.06e-03 | 3.37e-01 | 0.1017 |
Page: 1 2 3 4 5 |
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. |
Top |
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:0010498111 | Esophagus | ESCC | proteasomal protein catabolic process | 369/8552 | 490/18723 | 1.13e-41 | 1.80e-38 | 369 |
GO:0043161111 | Esophagus | ESCC | proteasome-mediated ubiquitin-dependent protein catabolic process | 312/8552 | 412/18723 | 3.53e-36 | 4.48e-33 | 312 |
GO:0006417111 | Esophagus | ESCC | regulation of translation | 304/8552 | 468/18723 | 1.53e-17 | 1.33e-15 | 304 |
GO:00065136 | Esophagus | ESCC | protein monoubiquitination | 53/8552 | 67/18723 | 2.11e-08 | 4.03e-07 | 53 |
GO:000641419 | Esophagus | ESCC | translational elongation | 41/8552 | 55/18723 | 1.26e-05 | 1.16e-04 | 41 |
GO:001049822 | Liver | HCC | proteasomal protein catabolic process | 351/7958 | 490/18723 | 6.92e-40 | 1.46e-36 | 351 |
GO:004316122 | Liver | HCC | proteasome-mediated ubiquitin-dependent protein catabolic process | 299/7958 | 412/18723 | 7.82e-36 | 8.27e-33 | 299 |
GO:000641722 | Liver | HCC | regulation of translation | 287/7958 | 468/18723 | 8.79e-17 | 8.08e-15 | 287 |
GO:000651311 | Liver | HCC | protein monoubiquitination | 44/7958 | 67/18723 | 1.08e-04 | 9.22e-04 | 44 |
GO:000641412 | Liver | HCC | translational elongation | 36/7958 | 55/18723 | 4.94e-04 | 3.23e-03 | 36 |
GO:001049820 | Oral cavity | OSCC | proteasomal protein catabolic process | 336/7305 | 490/18723 | 5.45e-41 | 8.63e-38 | 336 |
GO:004316120 | Oral cavity | OSCC | proteasome-mediated ubiquitin-dependent protein catabolic process | 285/7305 | 412/18723 | 5.68e-36 | 5.99e-33 | 285 |
GO:000641720 | Oral cavity | OSCC | regulation of translation | 274/7305 | 468/18723 | 4.39e-18 | 4.63e-16 | 274 |
GO:00065135 | Oral cavity | OSCC | protein monoubiquitination | 47/7305 | 67/18723 | 2.32e-07 | 3.68e-06 | 47 |
GO:000641416 | Oral cavity | OSCC | translational elongation | 37/7305 | 55/18723 | 2.03e-05 | 1.94e-04 | 37 |
GO:0010498110 | Oral cavity | LP | proteasomal protein catabolic process | 224/4623 | 490/18723 | 9.57e-25 | 4.00e-22 | 224 |
GO:0043161110 | Oral cavity | LP | proteasome-mediated ubiquitin-dependent protein catabolic process | 190/4623 | 412/18723 | 1.08e-21 | 2.93e-19 | 190 |
GO:0006417110 | Oral cavity | LP | regulation of translation | 175/4623 | 468/18723 | 4.49e-10 | 2.22e-08 | 175 |
GO:000641417 | Oral cavity | LP | translational elongation | 25/4623 | 55/18723 | 6.27e-04 | 5.71e-03 | 25 |
GO:000651313 | Oral cavity | LP | protein monoubiquitination | 29/4623 | 67/18723 | 6.51e-04 | 5.90e-03 | 29 |
Page: 1 2 |
Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
Page: 1 |
Top |
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 |
Top |
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 |
Top |
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 |
ZNF598 | SNV | Missense_Mutation | rs761148339 | c.2467G>A | p.Asp823Asn | p.D823N | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-BH-A1FM-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
ZNF598 | SNV | Missense_Mutation | rs746185966 | c.457C>T | p.Arg153Cys | p.R153C | protein_coding | deleterious(0) | probably_damaging(0.962) | TCGA-C8-A3M7-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD | |
ZNF598 | insertion | Nonsense_Mutation | novel | c.155_156insAGAGCCAGGCTTCTGACCCAGGCCATGTGCACAGCCATG | p.Val52_Tyr53insGluProGlyPheTerProArgProCysAlaGlnProTrp | p.V52_Y53insEPGF*PRPCAQPW | protein_coding | TCGA-A2-A0CP-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | |||
ZNF598 | SNV | Missense_Mutation | c.1085N>T | p.Ser362Leu | p.S362L | protein_coding | deleterious(0.02) | benign(0.001) | TCGA-DG-A2KM-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | SD | ||
ZNF598 | SNV | Missense_Mutation | novel | c.1804C>A | p.Leu602Met | p.L602M | protein_coding | tolerated(0.1) | benign(0.094) | TCGA-A6-3809-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
ZNF598 | SNV | Missense_Mutation | novel | c.910G>C | p.Glu304Gln | p.E304Q | protein_coding | tolerated(0.4) | benign(0.05) | TCGA-AA-3947-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ZNF598 | SNV | Missense_Mutation | c.833G>A | p.Ser278Asn | p.S278N | protein_coding | tolerated(0.05) | probably_damaging(0.996) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | ||
ZNF598 | SNV | Missense_Mutation | rs758722408 | c.2459C>T | p.Ala820Val | p.A820V | protein_coding | deleterious(0.01) | possibly_damaging(0.715) | TCGA-CM-4746-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
ZNF598 | SNV | Missense_Mutation | rs776908919 | c.1927N>T | p.Pro643Ser | p.P643S | protein_coding | deleterious(0.04) | probably_damaging(0.999) | TCGA-CM-5861-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | PD | |
ZNF598 | insertion | Frame_Shift_Ins | novel | c.1934_1935insC | p.Pro646AlafsTer20 | p.P646Afs*20 | protein_coding | TCGA-A6-5665-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
Page: 1 2 3 4 5 6 7 8 |
Top |
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 |
Page: 1 |