![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: NPHP3 |
Gene summary for NPHP3 |
![]() |
Gene information | Species | Human | Gene symbol | NPHP3 | Gene ID | 27031 |
Gene name | nephrocystin 3 | |
Gene Alias | CFAP31 | |
Cytomap | 3q22.1 | |
Gene Type | protein-coding | GO ID | GO:0001655 | UniProtAcc | Q7Z494 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
27031 | NPHP3 | HTA11_3410_2000001011 | Human | Colorectum | AD | 5.90e-11 | 2.46e-01 | 0.0155 |
27031 | NPHP3 | HTA11_2487_2000001011 | Human | Colorectum | SER | 6.13e-19 | 4.62e-01 | -0.1808 |
27031 | NPHP3 | HTA11_2951_2000001011 | Human | Colorectum | AD | 3.22e-05 | 3.36e-01 | 0.0216 |
27031 | NPHP3 | HTA11_1938_2000001011 | Human | Colorectum | AD | 4.60e-24 | 6.33e-01 | -0.0811 |
27031 | NPHP3 | HTA11_78_2000001011 | Human | Colorectum | AD | 7.85e-13 | 3.92e-01 | -0.1088 |
27031 | NPHP3 | HTA11_347_2000001011 | Human | Colorectum | AD | 5.98e-43 | 7.58e-01 | -0.1954 |
27031 | NPHP3 | HTA11_411_2000001011 | Human | Colorectum | SER | 1.86e-06 | 3.68e-01 | -0.2602 |
27031 | NPHP3 | HTA11_2112_2000001011 | Human | Colorectum | SER | 1.71e-03 | 3.67e-01 | -0.2196 |
27031 | NPHP3 | HTA11_3361_2000001011 | Human | Colorectum | AD | 9.32e-14 | 3.99e-01 | -0.1207 |
27031 | NPHP3 | HTA11_83_2000001011 | Human | Colorectum | SER | 2.45e-18 | 4.88e-01 | -0.1526 |
27031 | NPHP3 | HTA11_696_2000001011 | Human | Colorectum | AD | 9.02e-22 | 3.75e-01 | -0.1464 |
27031 | NPHP3 | HTA11_866_2000001011 | Human | Colorectum | AD | 3.10e-42 | 6.75e-01 | -0.1001 |
27031 | NPHP3 | HTA11_1391_2000001011 | Human | Colorectum | AD | 5.12e-18 | 4.15e-01 | -0.059 |
27031 | NPHP3 | HTA11_2992_2000001011 | Human | Colorectum | SER | 1.72e-05 | 3.33e-01 | -0.1706 |
27031 | NPHP3 | HTA11_5216_2000001011 | Human | Colorectum | SER | 2.49e-08 | 4.15e-01 | -0.1462 |
27031 | NPHP3 | HTA11_546_2000001011 | Human | Colorectum | AD | 4.31e-15 | 5.06e-01 | -0.0842 |
27031 | NPHP3 | HTA11_9341_2000001011 | Human | Colorectum | SER | 1.35e-12 | 6.00e-01 | -0.00410000000000005 |
27031 | NPHP3 | HTA11_7862_2000001011 | Human | Colorectum | AD | 4.04e-16 | 6.27e-01 | -0.0179 |
27031 | NPHP3 | HTA11_866_3004761011 | Human | Colorectum | AD | 1.22e-19 | 3.85e-01 | 0.096 |
27031 | NPHP3 | HTA11_4255_2000001011 | Human | Colorectum | SER | 1.84e-10 | 5.85e-01 | 0.0446 |
Page: 1 2 3 |
![]() |
∗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:0048732 | Colorectum | AD | gland development | 149/3918 | 436/18723 | 6.07e-11 | 6.33e-09 | 149 |
GO:0061008 | Colorectum | AD | hepaticobiliary system development | 55/3918 | 150/18723 | 6.34e-06 | 1.59e-04 | 55 |
GO:0001889 | Colorectum | AD | liver development | 54/3918 | 147/18723 | 7.20e-06 | 1.77e-04 | 54 |
GO:0030111 | Colorectum | AD | regulation of Wnt signaling pathway | 102/3918 | 328/18723 | 8.51e-06 | 2.03e-04 | 102 |
GO:0016055 | Colorectum | AD | Wnt signaling pathway | 130/3918 | 444/18723 | 1.60e-05 | 3.37e-04 | 130 |
GO:0198738 | Colorectum | AD | cell-cell signaling by wnt | 130/3918 | 446/18723 | 2.02e-05 | 4.10e-04 | 130 |
GO:0060249 | Colorectum | AD | anatomical structure homeostasis | 94/3918 | 314/18723 | 9.37e-05 | 1.42e-03 | 94 |
GO:0060070 | Colorectum | AD | canonical Wnt signaling pathway | 90/3918 | 303/18723 | 1.76e-04 | 2.38e-03 | 90 |
GO:0001894 | Colorectum | AD | tissue homeostasis | 81/3918 | 268/18723 | 1.96e-04 | 2.62e-03 | 81 |
GO:0060828 | Colorectum | AD | regulation of canonical Wnt signaling pathway | 77/3918 | 253/18723 | 2.19e-04 | 2.87e-03 | 77 |
GO:0060562 | Colorectum | AD | epithelial tube morphogenesis | 93/3918 | 325/18723 | 5.65e-04 | 6.00e-03 | 93 |
GO:0014020 | Colorectum | AD | primary neural tube formation | 33/3918 | 94/18723 | 1.02e-03 | 9.50e-03 | 33 |
GO:0001841 | Colorectum | AD | neural tube formation | 35/3918 | 102/18723 | 1.16e-03 | 1.05e-02 | 35 |
GO:0045995 | Colorectum | AD | regulation of embryonic development | 24/3918 | 64/18723 | 1.72e-03 | 1.43e-02 | 24 |
GO:0001843 | Colorectum | AD | neural tube closure | 30/3918 | 88/18723 | 2.83e-03 | 2.12e-02 | 30 |
GO:0060606 | Colorectum | AD | tube closure | 30/3918 | 89/18723 | 3.42e-03 | 2.49e-02 | 30 |
GO:0035148 | Colorectum | AD | tube formation | 45/3918 | 148/18723 | 4.13e-03 | 2.87e-02 | 45 |
GO:0001738 | Colorectum | AD | morphogenesis of a polarized epithelium | 31/3918 | 94/18723 | 4.30e-03 | 2.95e-02 | 31 |
GO:0001838 | Colorectum | AD | embryonic epithelial tube formation | 38/3918 | 121/18723 | 4.40e-03 | 3.01e-02 | 38 |
GO:0048568 | Colorectum | AD | embryonic organ development | 112/3918 | 427/18723 | 4.60e-03 | 3.14e-02 | 112 |
Page: 1 2 3 4 5 6 7 8 |
![]() |
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 |
NPHP3 | SNV | Missense_Mutation | novel | c.1655N>A | p.Pro552His | p.P552H | Q7Z494 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A7-A0DB-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | arimidex | SD |
NPHP3 | SNV | Missense_Mutation | rs758498695 | c.988N>A | p.Glu330Lys | p.E330K | Q7Z494 | protein_coding | deleterious(0.03) | probably_damaging(0.969) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
NPHP3 | SNV | Missense_Mutation | c.790N>C | p.Asp264His | p.D264H | Q7Z494 | protein_coding | deleterious(0) | probably_damaging(0.937) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
NPHP3 | SNV | Missense_Mutation | c.688N>C | p.Glu230Gln | p.E230Q | Q7Z494 | protein_coding | tolerated(0.05) | benign(0.177) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
NPHP3 | insertion | Frame_Shift_Ins | novel | c.1752_1753insATATATGTGT | p.His585IlefsTer17 | p.H585Ifs*17 | Q7Z494 | protein_coding | TCGA-A8-A0A4-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | CR | ||
NPHP3 | SNV | Missense_Mutation | c.2800N>A | p.Glu934Lys | p.E934K | Q7Z494 | protein_coding | tolerated(0.34) | benign(0.078) | TCGA-EK-A2PG-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
NPHP3 | SNV | Missense_Mutation | rs150867534 | c.2986N>A | p.Val996Met | p.V996M | Q7Z494 | protein_coding | tolerated(0.18) | benign(0.059) | TCGA-A6-6654-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | oxaliplatin | SD |
NPHP3 | SNV | Missense_Mutation | c.982N>C | p.Met328Leu | p.M328L | Q7Z494 | protein_coding | tolerated(0.85) | benign(0) | TCGA-AA-3982-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | |
NPHP3 | SNV | Missense_Mutation | novel | c.2383T>G | p.Ser795Ala | p.S795A | Q7Z494 | protein_coding | tolerated(0.14) | benign(0.005) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR |
NPHP3 | SNV | Missense_Mutation | c.1432N>A | p.Gly478Ser | p.G478S | Q7Z494 | protein_coding | tolerated(0.09) | possibly_damaging(0.833) | TCGA-AA-A022-01 | 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 |