![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: NDST1 |
Gene summary for NDST1 |
![]() |
Gene information | Species | Human | Gene symbol | NDST1 | Gene ID | 3340 |
Gene name | N-deacetylase and N-sulfotransferase 1 | |
Gene Alias | HSST | |
Cytomap | 5q33.1 | |
Gene Type | protein-coding | GO ID | GO:0000165 | UniProtAcc | B7Z1Q0 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
3340 | NDST1 | LZE24T | Human | Esophagus | ESCC | 3.85e-02 | 8.68e-02 | 0.0596 |
3340 | NDST1 | P2T-E | Human | Esophagus | ESCC | 9.72e-07 | 1.14e-01 | 0.1177 |
3340 | NDST1 | P5T-E | Human | Esophagus | ESCC | 5.50e-08 | 9.51e-02 | 0.1327 |
3340 | NDST1 | P8T-E | Human | Esophagus | ESCC | 2.17e-07 | 7.37e-02 | 0.0889 |
3340 | NDST1 | P9T-E | Human | Esophagus | ESCC | 8.59e-06 | 1.28e-01 | 0.1131 |
3340 | NDST1 | P10T-E | Human | Esophagus | ESCC | 5.99e-03 | 8.35e-02 | 0.116 |
3340 | NDST1 | P11T-E | Human | Esophagus | ESCC | 1.37e-07 | 3.34e-01 | 0.1426 |
3340 | NDST1 | P12T-E | Human | Esophagus | ESCC | 6.62e-06 | 1.46e-01 | 0.1122 |
3340 | NDST1 | P15T-E | Human | Esophagus | ESCC | 2.50e-03 | 1.22e-01 | 0.1149 |
3340 | NDST1 | P16T-E | Human | Esophagus | ESCC | 9.22e-12 | 1.06e-01 | 0.1153 |
3340 | NDST1 | P17T-E | Human | Esophagus | ESCC | 4.06e-04 | 1.49e-01 | 0.1278 |
3340 | NDST1 | P19T-E | Human | Esophagus | ESCC | 3.58e-05 | 3.34e-01 | 0.1662 |
3340 | NDST1 | P21T-E | Human | Esophagus | ESCC | 6.69e-13 | 1.70e-01 | 0.1617 |
3340 | NDST1 | P22T-E | Human | Esophagus | ESCC | 1.91e-09 | 9.90e-02 | 0.1236 |
3340 | NDST1 | P23T-E | Human | Esophagus | ESCC | 1.25e-04 | 9.99e-02 | 0.108 |
3340 | NDST1 | P24T-E | Human | Esophagus | ESCC | 4.13e-06 | 8.47e-02 | 0.1287 |
3340 | NDST1 | P26T-E | Human | Esophagus | ESCC | 1.40e-05 | 7.42e-02 | 0.1276 |
3340 | NDST1 | P27T-E | Human | Esophagus | ESCC | 3.35e-11 | 1.26e-01 | 0.1055 |
3340 | NDST1 | P28T-E | Human | Esophagus | ESCC | 2.41e-09 | 1.79e-01 | 0.1149 |
3340 | NDST1 | P30T-E | Human | Esophagus | ESCC | 1.76e-07 | 2.65e-01 | 0.137 |
Page: 1 2 3 4 |
![]() |
∗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:00091002 | Esophagus | ESCC | glycoprotein metabolic process | 226/8552 | 387/18723 | 2.64e-07 | 3.94e-06 | 226 |
GO:00067906 | Esophagus | ESCC | sulfur compound metabolic process | 201/8552 | 339/18723 | 2.64e-07 | 3.94e-06 | 201 |
GO:00442725 | Esophagus | ESCC | sulfur compound biosynthetic process | 96/8552 | 148/18723 | 1.86e-06 | 2.16e-05 | 96 |
GO:00091012 | Esophagus | ESCC | glycoprotein biosynthetic process | 181/8552 | 317/18723 | 2.54e-05 | 2.15e-04 | 181 |
GO:00442626 | Esophagus | ESCC | cellular carbohydrate metabolic process | 160/8552 | 283/18723 | 1.43e-04 | 9.66e-04 | 160 |
GO:003090118 | Esophagus | ESCC | midbrain development | 58/8552 | 90/18723 | 2.52e-04 | 1.55e-03 | 58 |
GO:00160514 | Esophagus | ESCC | carbohydrate biosynthetic process | 117/8552 | 202/18723 | 2.96e-04 | 1.79e-03 | 117 |
GO:00485687 | Esophagus | ESCC | embryonic organ development | 228/8552 | 427/18723 | 7.28e-04 | 3.79e-03 | 228 |
GO:00487052 | Esophagus | ESCC | skeletal system morphogenesis | 120/8552 | 220/18723 | 4.90e-03 | 1.89e-02 | 120 |
GO:0006029 | Esophagus | ESCC | proteoglycan metabolic process | 48/8552 | 79/18723 | 4.93e-03 | 1.89e-02 | 48 |
GO:0030166 | Esophagus | ESCC | proteoglycan biosynthetic process | 35/8552 | 56/18723 | 8.30e-03 | 2.94e-02 | 35 |
GO:0006024 | Esophagus | ESCC | glycosaminoglycan biosynthetic process | 45/8552 | 75/18723 | 8.75e-03 | 3.08e-02 | 45 |
GO:0006023 | Esophagus | ESCC | aminoglycan biosynthetic process | 47/8552 | 79/18723 | 9.29e-03 | 3.23e-02 | 47 |
GO:19048881 | Esophagus | ESCC | cranial skeletal system development | 41/8552 | 68/18723 | 1.07e-02 | 3.66e-02 | 41 |
GO:0030201 | Esophagus | ESCC | heparan sulfate proteoglycan metabolic process | 21/8552 | 31/18723 | 1.10e-02 | 3.70e-02 | 21 |
GO:00346372 | Esophagus | ESCC | cellular carbohydrate biosynthetic process | 46/8552 | 78/18723 | 1.24e-02 | 4.13e-02 | 46 |
GO:00442623 | Liver | NAFLD | cellular carbohydrate metabolic process | 55/1882 | 283/18723 | 1.27e-06 | 6.01e-05 | 55 |
GO:0016051 | Liver | NAFLD | carbohydrate biosynthetic process | 43/1882 | 202/18723 | 1.55e-06 | 6.96e-05 | 43 |
GO:00067904 | Liver | NAFLD | sulfur compound metabolic process | 58/1882 | 339/18723 | 3.79e-05 | 9.38e-04 | 58 |
GO:0034637 | Liver | NAFLD | cellular carbohydrate biosynthetic process | 20/1882 | 78/18723 | 6.46e-05 | 1.39e-03 | 20 |
Page: 1 2 3 4 |
![]() |
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 |
NDST1 | SNV | Missense_Mutation | rs747996016 | c.986G>A | p.Arg329His | p.R329H | P52848 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-EA-A410-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
NDST1 | SNV | Missense_Mutation | c.1817N>C | p.Lys606Thr | p.K606T | P52848 | protein_coding | deleterious(0) | probably_damaging(0.923) | TCGA-A6-5665-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
NDST1 | SNV | Missense_Mutation | rs573765554 | c.2447T>G | p.Phe816Cys | p.F816C | P52848 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
NDST1 | SNV | Missense_Mutation | rs776984233 | c.1030N>A | p.Glu344Lys | p.E344K | P52848 | protein_coding | tolerated(0.92) | benign(0) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
NDST1 | SNV | Missense_Mutation | c.1307T>C | p.Val436Ala | p.V436A | P52848 | protein_coding | deleterious(0.03) | benign(0.19) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
NDST1 | SNV | Missense_Mutation | rs141752622 | c.2249N>A | p.Arg750His | p.R750H | P52848 | protein_coding | tolerated(0.05) | benign(0.175) | TCGA-CK-6751-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
NDST1 | SNV | Missense_Mutation | rs754297456 | c.1409N>A | p.Arg470His | p.R470H | P52848 | protein_coding | deleterious(0) | probably_damaging(0.967) | TCGA-D5-5541-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | calcium | SD |
NDST1 | SNV | Missense_Mutation | c.344N>A | p.Ile115Asn | p.I115N | P52848 | protein_coding | deleterious(0) | probably_damaging(0.987) | TCGA-G4-6304-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Chemotherapy | fluorouracil | PD | |
NDST1 | SNV | Missense_Mutation | rs770655306 | c.238C>T | p.Arg80Cys | p.R80C | P52848 | protein_coding | deleterious(0) | probably_damaging(0.977) | TCGA-NH-A5IV-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
NDST1 | SNV | Missense_Mutation | c.623A>G | p.Tyr208Cys | p.Y208C | P52848 | protein_coding | tolerated(0.12) | probably_damaging(0.928) | TCGA-NH-A5IV-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
Page: 1 2 3 4 5 6 7 8 9 10 |
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 |