![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: ZPR1 |
Gene summary for ZPR1 |
![]() |
Gene information | Species | Human | Gene symbol | ZPR1 | Gene ID | 8882 |
Gene name | ZPR1 zinc finger | |
Gene Alias | GKAF | |
Cytomap | 11q23.3 | |
Gene Type | protein-coding | GO ID | GO:0000082 | UniProtAcc | O75312 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
8882 | ZPR1 | LZE4T | Human | Esophagus | ESCC | 1.08e-09 | 1.77e-01 | 0.0811 |
8882 | ZPR1 | LZE7T | Human | Esophagus | ESCC | 2.04e-02 | 1.10e-01 | 0.0667 |
8882 | ZPR1 | LZE20T | Human | Esophagus | ESCC | 2.57e-08 | 1.29e-01 | 0.0662 |
8882 | ZPR1 | LZE24T | Human | Esophagus | ESCC | 7.00e-29 | 1.03e+00 | 0.0596 |
8882 | ZPR1 | LZE21T | Human | Esophagus | ESCC | 2.83e-02 | 1.09e-01 | 0.0655 |
8882 | ZPR1 | P1T-E | Human | Esophagus | ESCC | 3.28e-07 | 1.74e-01 | 0.0875 |
8882 | ZPR1 | P2T-E | Human | Esophagus | ESCC | 6.54e-15 | 2.70e-01 | 0.1177 |
8882 | ZPR1 | P4T-E | Human | Esophagus | ESCC | 1.80e-30 | 9.69e-01 | 0.1323 |
8882 | ZPR1 | P5T-E | Human | Esophagus | ESCC | 4.44e-26 | 5.86e-01 | 0.1327 |
8882 | ZPR1 | P8T-E | Human | Esophagus | ESCC | 6.71e-12 | 1.31e-01 | 0.0889 |
8882 | ZPR1 | P9T-E | Human | Esophagus | ESCC | 5.17e-21 | 4.25e-01 | 0.1131 |
8882 | ZPR1 | P10T-E | Human | Esophagus | ESCC | 2.62e-23 | 5.26e-01 | 0.116 |
8882 | ZPR1 | P11T-E | Human | Esophagus | ESCC | 1.56e-13 | 7.15e-01 | 0.1426 |
8882 | ZPR1 | P12T-E | Human | Esophagus | ESCC | 1.11e-30 | 6.10e-01 | 0.1122 |
8882 | ZPR1 | P15T-E | Human | Esophagus | ESCC | 3.53e-13 | 3.55e-01 | 0.1149 |
8882 | ZPR1 | P16T-E | Human | Esophagus | ESCC | 3.04e-17 | 3.91e-01 | 0.1153 |
8882 | ZPR1 | P17T-E | Human | Esophagus | ESCC | 6.32e-03 | 4.76e-01 | 0.1278 |
8882 | ZPR1 | P19T-E | Human | Esophagus | ESCC | 2.40e-10 | 5.76e-01 | 0.1662 |
8882 | ZPR1 | P20T-E | Human | Esophagus | ESCC | 1.13e-16 | 3.42e-01 | 0.1124 |
8882 | ZPR1 | P21T-E | Human | Esophagus | ESCC | 8.52e-41 | 9.79e-01 | 0.1617 |
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:003465521 | Liver | HCC | nucleobase-containing compound catabolic process | 273/7958 | 407/18723 | 4.84e-24 | 1.23e-21 | 273 |
GO:190382922 | Liver | HCC | positive regulation of cellular protein localization | 199/7958 | 276/18723 | 1.15e-23 | 2.62e-21 | 199 |
GO:003238621 | Liver | HCC | regulation of intracellular transport | 231/7958 | 337/18723 | 1.99e-22 | 3.40e-20 | 231 |
GO:000691322 | Liver | HCC | nucleocytoplasmic transport | 208/7958 | 301/18723 | 5.51e-21 | 8.12e-19 | 208 |
GO:005116922 | Liver | HCC | nuclear transport | 208/7958 | 301/18723 | 5.51e-21 | 8.12e-19 | 208 |
GO:003315721 | Liver | HCC | regulation of intracellular protein transport | 165/7958 | 229/18723 | 8.37e-20 | 1.15e-17 | 165 |
GO:003238821 | Liver | HCC | positive regulation of intracellular transport | 148/7958 | 202/18723 | 5.15e-19 | 6.66e-17 | 148 |
GO:009031621 | Liver | HCC | positive regulation of intracellular protein transport | 121/7958 | 160/18723 | 1.27e-17 | 1.39e-15 | 121 |
GO:003450421 | Liver | HCC | protein localization to nucleus | 194/7958 | 290/18723 | 2.84e-17 | 2.85e-15 | 194 |
GO:004348422 | Liver | HCC | regulation of RNA splicing | 113/7958 | 148/18723 | 4.32e-17 | 4.15e-15 | 113 |
GO:190495122 | Liver | HCC | positive regulation of establishment of protein localization | 207/7958 | 319/18723 | 3.95e-16 | 3.29e-14 | 207 |
GO:005122222 | Liver | HCC | positive regulation of protein transport | 194/7958 | 303/18723 | 2.41e-14 | 1.56e-12 | 194 |
GO:001703811 | Liver | HCC | protein import | 140/7958 | 206/18723 | 1.12e-13 | 6.46e-12 | 140 |
GO:004682221 | Liver | HCC | regulation of nucleocytoplasmic transport | 81/7958 | 106/18723 | 1.11e-12 | 5.52e-11 | 81 |
GO:190018212 | Liver | HCC | positive regulation of protein localization to nucleus | 67/7958 | 87/18723 | 5.43e-11 | 2.00e-09 | 67 |
GO:190018012 | Liver | HCC | regulation of protein localization to nucleus | 95/7958 | 136/18723 | 9.26e-11 | 3.26e-09 | 95 |
GO:00447722 | Liver | HCC | mitotic cell cycle phase transition | 240/7958 | 424/18723 | 2.47e-09 | 6.84e-08 | 240 |
GO:005117011 | Liver | HCC | import into nucleus | 102/7958 | 159/18723 | 2.78e-08 | 6.39e-07 | 102 |
GO:00066066 | Liver | HCC | protein import into nucleus | 99/7958 | 155/18723 | 6.12e-08 | 1.28e-06 | 99 |
GO:007099722 | Liver | HCC | neuron death | 202/7958 | 361/18723 | 1.44e-07 | 2.70e-06 | 202 |
Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 |
![]() |
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 |
ZPR1 | SNV | Missense_Mutation | rs148642555 | c.1376N>A | p.Arg459Gln | p.R459Q | O75312 | protein_coding | tolerated_low_confidence(0.06) | probably_damaging(0.978) | TCGA-D8-A1XK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicine+cyclophosphamide | SD |
ZPR1 | SNV | Missense_Mutation | novel | c.1170N>T | p.Lys390Asn | p.K390N | O75312 | protein_coding | deleterious(0.04) | probably_damaging(0.923) | TCGA-D8-A4Z1-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | SD |
ZPR1 | SNV | Missense_Mutation | novel | c.346N>A | p.Glu116Lys | p.E116K | O75312 | protein_coding | deleterious(0.02) | benign(0.41) | TCGA-EW-A1OV-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | epirubicin | SD |
ZPR1 | SNV | Missense_Mutation | novel | c.509C>T | p.Ala170Val | p.A170V | O75312 | protein_coding | deleterious(0.05) | benign(0.053) | TCGA-ZJ-A8QR-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
ZPR1 | SNV | Missense_Mutation | c.233N>C | p.Phe78Ser | p.F78S | O75312 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-3492-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
ZPR1 | SNV | Missense_Mutation | c.521N>T | p.Arg174Ile | p.R174I | O75312 | protein_coding | deleterious(0) | possibly_damaging(0.465) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ZPR1 | SNV | Missense_Mutation | novel | c.763N>C | p.Phe255Leu | p.F255L | O75312 | protein_coding | deleterious(0) | possibly_damaging(0.694) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD |
ZPR1 | SNV | Missense_Mutation | c.521G>T | p.Arg174Ile | p.R174I | O75312 | protein_coding | deleterious(0) | possibly_damaging(0.465) | TCGA-CA-6718-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | PD | |
ZPR1 | SNV | Missense_Mutation | rs529843898 | c.796N>A | p.Ala266Thr | p.A266T | O75312 | protein_coding | tolerated(0.16) | benign(0.095) | TCGA-F4-6856-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Ancillary | leucovorin | CR |
ZPR1 | SNV | Missense_Mutation | c.521N>T | p.Arg174Ile | p.R174I | O75312 | protein_coding | deleterious(0) | possibly_damaging(0.465) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <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 |
Page: 1 |