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Gene: CFAP36 |
Gene summary for CFAP36 |
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Gene information | Species | Human | Gene symbol | CFAP36 | Gene ID | 112942 |
Gene name | cilia and flagella associated protein 36 | |
Gene Alias | BARTL1 | |
Cytomap | 2p16.1 | |
Gene Type | protein-coding | GO ID | GO:0008150 | UniProtAcc | Q96G28 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
112942 | CFAP36 | LZE4T | Human | Esophagus | ESCC | 2.53e-08 | 3.74e-01 | 0.0811 |
112942 | CFAP36 | LZE5T | Human | Esophagus | ESCC | 9.10e-08 | 2.06e-01 | 0.0514 |
112942 | CFAP36 | LZE7T | Human | Esophagus | ESCC | 1.30e-02 | 3.79e-01 | 0.0667 |
112942 | CFAP36 | LZE8T | Human | Esophagus | ESCC | 4.96e-07 | 8.71e-02 | 0.067 |
112942 | CFAP36 | LZE24T | Human | Esophagus | ESCC | 5.97e-10 | 3.99e-01 | 0.0596 |
112942 | CFAP36 | P1T-E | Human | Esophagus | ESCC | 2.89e-08 | 3.22e-01 | 0.0875 |
112942 | CFAP36 | P2T-E | Human | Esophagus | ESCC | 1.34e-57 | 1.06e+00 | 0.1177 |
112942 | CFAP36 | P4T-E | Human | Esophagus | ESCC | 8.81e-31 | 8.01e-01 | 0.1323 |
112942 | CFAP36 | P5T-E | Human | Esophagus | ESCC | 1.09e-21 | 2.94e-01 | 0.1327 |
112942 | CFAP36 | P8T-E | Human | Esophagus | ESCC | 1.28e-15 | 3.09e-01 | 0.0889 |
112942 | CFAP36 | P9T-E | Human | Esophagus | ESCC | 1.65e-21 | 3.95e-01 | 0.1131 |
112942 | CFAP36 | P10T-E | Human | Esophagus | ESCC | 1.50e-23 | 5.14e-01 | 0.116 |
112942 | CFAP36 | P11T-E | Human | Esophagus | ESCC | 7.42e-18 | 5.70e-01 | 0.1426 |
112942 | CFAP36 | P12T-E | Human | Esophagus | ESCC | 5.08e-24 | 3.86e-01 | 0.1122 |
112942 | CFAP36 | P15T-E | Human | Esophagus | ESCC | 2.79e-17 | 4.39e-01 | 0.1149 |
112942 | CFAP36 | P16T-E | Human | Esophagus | ESCC | 1.43e-45 | 9.24e-01 | 0.1153 |
112942 | CFAP36 | P17T-E | Human | Esophagus | ESCC | 1.98e-08 | 3.39e-01 | 0.1278 |
112942 | CFAP36 | P19T-E | Human | Esophagus | ESCC | 2.23e-07 | 7.00e-01 | 0.1662 |
112942 | CFAP36 | P20T-E | Human | Esophagus | ESCC | 1.14e-22 | 4.51e-01 | 0.1124 |
112942 | CFAP36 | P21T-E | Human | Esophagus | ESCC | 3.32e-39 | 8.04e-01 | 0.1617 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
Page: 1 |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
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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 |
CFAP36 | SNV | Missense_Mutation | rs766105569 | c.496G>A | p.Asp166Asn | p.D166N | Q96G28 | protein_coding | deleterious(0.01) | benign(0.09) | TCGA-YL-A8SC-01 | Prostate | prostate adenocarcinoma | Male | >=65 | 9 | Hormone Therapy | casodex | PR |
CFAP36 | SNV | Missense_Mutation | c.1008N>T | p.Met336Ile | p.M336I | Q96G28 | protein_coding | tolerated(0.5) | benign(0.015) | TCGA-BR-8680-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | oxaliplatin | CR | |
CFAP36 | SNV | Missense_Mutation | c.58C>A | p.Leu20Met | p.L20M | Q96G28 | protein_coding | deleterious(0) | possibly_damaging(0.903) | TCGA-HU-A4GT-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Chemotherapy | copolang | 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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