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Gene: WDR36 |
Gene summary for WDR36 |
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Gene information | Species | Human | Gene symbol | WDR36 | Gene ID | 134430 |
Gene name | WD repeat domain 36 | |
Gene Alias | GLC1G | |
Cytomap | 5q22.1 | |
Gene Type | protein-coding | GO ID | GO:0003008 | UniProtAcc | Q8NI36 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
134430 | WDR36 | P21T-E | Human | Esophagus | ESCC | 6.98e-20 | 3.75e-01 | 0.1617 |
134430 | WDR36 | P22T-E | Human | Esophagus | ESCC | 9.72e-26 | 9.82e-02 | 0.1236 |
134430 | WDR36 | P23T-E | Human | Esophagus | ESCC | 1.22e-08 | 3.40e-01 | 0.108 |
134430 | WDR36 | P24T-E | Human | Esophagus | ESCC | 6.30e-16 | 2.35e-01 | 0.1287 |
134430 | WDR36 | P26T-E | Human | Esophagus | ESCC | 1.39e-17 | 1.46e-01 | 0.1276 |
134430 | WDR36 | P27T-E | Human | Esophagus | ESCC | 5.77e-13 | 1.76e-01 | 0.1055 |
134430 | WDR36 | P28T-E | Human | Esophagus | ESCC | 1.80e-05 | 8.39e-03 | 0.1149 |
134430 | WDR36 | P30T-E | Human | Esophagus | ESCC | 1.38e-15 | 4.80e-01 | 0.137 |
134430 | WDR36 | P31T-E | Human | Esophagus | ESCC | 1.66e-11 | 3.74e-02 | 0.1251 |
134430 | WDR36 | P32T-E | Human | Esophagus | ESCC | 1.13e-19 | 2.44e-01 | 0.1666 |
134430 | WDR36 | P36T-E | Human | Esophagus | ESCC | 5.34e-10 | 5.93e-01 | 0.1187 |
134430 | WDR36 | P37T-E | Human | Esophagus | ESCC | 3.58e-16 | 1.88e-01 | 0.1371 |
134430 | WDR36 | P39T-E | Human | Esophagus | ESCC | 3.99e-13 | 3.54e-02 | 0.0894 |
134430 | WDR36 | P40T-E | Human | Esophagus | ESCC | 2.58e-08 | 3.17e-02 | 0.109 |
134430 | WDR36 | P42T-E | Human | Esophagus | ESCC | 1.47e-17 | 1.92e-01 | 0.1175 |
134430 | WDR36 | P44T-E | Human | Esophagus | ESCC | 1.34e-06 | 5.62e-02 | 0.1096 |
134430 | WDR36 | P47T-E | Human | Esophagus | ESCC | 1.43e-08 | -9.10e-03 | 0.1067 |
134430 | WDR36 | P48T-E | Human | Esophagus | ESCC | 1.35e-08 | 1.00e-01 | 0.0959 |
134430 | WDR36 | P49T-E | Human | Esophagus | ESCC | 7.72e-07 | 3.94e-01 | 0.1768 |
134430 | WDR36 | P52T-E | Human | Esophagus | ESCC | 8.30e-16 | 3.46e-01 | 0.1555 |
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∗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. |
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Malignant transformation related pathway analysis |
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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). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:0022613111 | Esophagus | ESCC | ribonucleoprotein complex biogenesis | 365/8552 | 463/18723 | 1.74e-49 | 1.11e-45 | 365 |
GO:0042254111 | Esophagus | ESCC | ribosome biogenesis | 252/8552 | 299/18723 | 3.27e-44 | 1.04e-40 | 252 |
GO:003447015 | Esophagus | ESCC | ncRNA processing | 300/8552 | 395/18723 | 3.09e-35 | 3.26e-32 | 300 |
GO:0016072110 | Esophagus | ESCC | rRNA metabolic process | 197/8552 | 236/18723 | 1.31e-33 | 1.18e-30 | 197 |
GO:0006364110 | Esophagus | ESCC | rRNA processing | 189/8552 | 225/18723 | 4.88e-33 | 3.87e-30 | 189 |
GO:003466012 | Esophagus | ESCC | ncRNA metabolic process | 346/8552 | 485/18723 | 4.35e-31 | 2.51e-28 | 346 |
GO:002261322 | Liver | HCC | ribonucleoprotein complex biogenesis | 355/7958 | 463/18723 | 7.76e-52 | 4.92e-48 | 355 |
GO:004225422 | Liver | HCC | ribosome biogenesis | 246/7958 | 299/18723 | 4.99e-46 | 1.58e-42 | 246 |
GO:00344702 | Liver | HCC | ncRNA processing | 293/7958 | 395/18723 | 4.26e-38 | 6.76e-35 | 293 |
GO:001607212 | Liver | HCC | rRNA metabolic process | 193/7958 | 236/18723 | 1.26e-35 | 1.14e-32 | 193 |
GO:000636421 | Liver | HCC | rRNA processing | 185/7958 | 225/18723 | 8.14e-35 | 6.45e-32 | 185 |
GO:00346601 | Liver | HCC | ncRNA metabolic process | 332/7958 | 485/18723 | 1.48e-31 | 7.80e-29 | 332 |
GO:002261320 | Oral cavity | OSCC | ribonucleoprotein complex biogenesis | 333/7305 | 463/18723 | 8.28e-48 | 5.24e-44 | 333 |
GO:004225420 | Oral cavity | OSCC | ribosome biogenesis | 230/7305 | 299/18723 | 3.22e-41 | 6.80e-38 | 230 |
GO:000636410 | Oral cavity | OSCC | rRNA processing | 172/7305 | 225/18723 | 1.57e-30 | 1.24e-27 | 172 |
GO:00344709 | Oral cavity | OSCC | ncRNA processing | 263/7305 | 395/18723 | 4.38e-29 | 2.78e-26 | 263 |
GO:001607210 | Oral cavity | OSCC | rRNA metabolic process | 176/7305 | 236/18723 | 6.51e-29 | 3.24e-26 | 176 |
GO:00346605 | Oral cavity | OSCC | ncRNA metabolic process | 296/7305 | 485/18723 | 2.94e-23 | 6.65e-21 | 296 |
GO:002261329 | Skin | cSCC | ribonucleoprotein complex biogenesis | 302/4864 | 463/18723 | 5.13e-72 | 3.22e-68 | 302 |
GO:004225428 | Skin | cSCC | ribosome biogenesis | 206/4864 | 299/18723 | 3.33e-55 | 1.04e-51 | 206 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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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. |
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Somatic mutation of malignant transformation related genes |
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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 |
WDR36 | SNV | Missense_Mutation | c.1606N>G | p.Gln536Glu | p.Q536E | Q8NI36 | protein_coding | tolerated(0.36) | benign(0.006) | TCGA-A8-A08R-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
WDR36 | SNV | Missense_Mutation | rs752635516 | c.68T>G | p.Leu23Arg | p.L23R | Q8NI36 | protein_coding | tolerated_low_confidence(0.41) | benign(0) | TCGA-BH-A8FZ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
WDR36 | SNV | Missense_Mutation | c.2068N>G | p.Leu690Val | p.L690V | Q8NI36 | protein_coding | deleterious(0) | possibly_damaging(0.723) | TCGA-EW-A1J5-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | |
WDR36 | deletion | Frame_Shift_Del | novel | c.1817delN | p.Leu607TrpfsTer3 | p.L607Wfs*3 | Q8NI36 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD | ||
WDR36 | SNV | Missense_Mutation | novel | c.2637N>T | p.Met879Ile | p.M879I | Q8NI36 | protein_coding | tolerated(0.07) | possibly_damaging(0.796) | TCGA-DG-A2KJ-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
WDR36 | SNV | Missense_Mutation | c.1087G>C | p.Asp363His | p.D363H | Q8NI36 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-EK-A2PL-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Unknown | Unknown | SD | |
WDR36 | SNV | Missense_Mutation | c.1351N>A | p.Glu451Lys | p.E451K | Q8NI36 | protein_coding | tolerated(0.39) | benign(0.024) | TCGA-EK-A2RA-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
WDR36 | SNV | Missense_Mutation | c.42G>T | p.Gln14His | p.Q14H | Q8NI36 | protein_coding | tolerated_low_confidence(0.12) | benign(0) | TCGA-AA-3530-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
WDR36 | SNV | Missense_Mutation | novel | c.1636N>A | p.Ala546Thr | p.A546T | Q8NI36 | protein_coding | tolerated(0.1) | probably_damaging(0.927) | TCGA-AA-3947-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
WDR36 | SNV | Missense_Mutation | c.811G>T | p.Val271Phe | p.V271F | Q8NI36 | protein_coding | deleterious(0) | benign(0.167) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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