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Gene: CFAP97 |
Gene summary for CFAP97 |
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Gene information | Species | Human | Gene symbol | CFAP97 | Gene ID | 57587 |
Gene name | cilia and flagella associated protein 97 | |
Gene Alias | KIAA1430 | |
Cytomap | 4q35.1 | |
Gene Type | protein-coding | GO ID | NA | UniProtAcc | Q9P2B7 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
57587 | CFAP97 | C04 | Human | Oral cavity | OSCC | 5.73e-12 | 6.98e-01 | 0.2633 |
57587 | CFAP97 | C21 | Human | Oral cavity | OSCC | 1.08e-29 | 1.24e+00 | 0.2678 |
57587 | CFAP97 | C30 | Human | Oral cavity | OSCC | 7.08e-16 | 9.50e-01 | 0.3055 |
57587 | CFAP97 | C38 | Human | Oral cavity | OSCC | 3.06e-02 | 5.87e-01 | 0.172 |
57587 | CFAP97 | C43 | Human | Oral cavity | OSCC | 9.13e-25 | 5.54e-01 | 0.1704 |
57587 | CFAP97 | C46 | Human | Oral cavity | OSCC | 7.92e-12 | 5.64e-01 | 0.1673 |
57587 | CFAP97 | C51 | Human | Oral cavity | OSCC | 8.32e-04 | 5.52e-01 | 0.2674 |
57587 | CFAP97 | C08 | Human | Oral cavity | OSCC | 1.71e-34 | 8.49e-01 | 0.1919 |
57587 | CFAP97 | C09 | Human | Oral cavity | OSCC | 2.01e-10 | 3.10e-01 | 0.1431 |
57587 | CFAP97 | LN22 | Human | Oral cavity | OSCC | 8.79e-04 | 4.81e-01 | 0.1733 |
57587 | CFAP97 | LN46 | Human | Oral cavity | OSCC | 4.31e-06 | 4.52e-01 | 0.1666 |
57587 | CFAP97 | SYSMH1 | Human | Oral cavity | OSCC | 7.76e-03 | 1.88e-01 | 0.1127 |
57587 | CFAP97 | SYSMH2 | Human | Oral cavity | OSCC | 8.05e-11 | 5.24e-01 | 0.2326 |
57587 | CFAP97 | SYSMH3 | Human | Oral cavity | OSCC | 1.35e-19 | 7.18e-01 | 0.2442 |
57587 | CFAP97 | SYSMH4 | Human | Oral cavity | OSCC | 1.36e-03 | 7.61e-02 | 0.1226 |
57587 | CFAP97 | male-WTA | Human | Thyroid | PTC | 6.03e-43 | 5.12e-01 | 0.1037 |
57587 | CFAP97 | PTC01 | Human | Thyroid | PTC | 1.56e-23 | 5.22e-01 | 0.1899 |
57587 | CFAP97 | PTC03 | Human | Thyroid | PTC | 2.86e-05 | 3.23e-01 | 0.1784 |
57587 | CFAP97 | PTC04 | Human | Thyroid | PTC | 7.57e-25 | 6.34e-01 | 0.1927 |
57587 | CFAP97 | PTC05 | Human | Thyroid | PTC | 2.60e-34 | 1.36e+00 | 0.2065 |
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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 |
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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 |
CFAP97 | SNV | Missense_Mutation | rs781085964 | c.1205C>T | p.Ala402Val | p.A402V | Q9P2B7 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
CFAP97 | SNV | Missense_Mutation | c.615N>T | p.Lys205Asn | p.K205N | Q9P2B7 | protein_coding | tolerated(0.32) | benign(0.001) | TCGA-D8-A27W-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicine+cyclophosphamide | SD | |
CFAP97 | SNV | Missense_Mutation | c.608N>T | p.Ser203Leu | p.S203L | Q9P2B7 | protein_coding | tolerated(0.1) | benign(0.036) | TCGA-E2-A14V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD | |
CFAP97 | insertion | Nonsense_Mutation | novel | c.825_826insCATTCCCAACAATAAAAAATATCTACTA | p.Asp276HisfsTer5 | p.D276Hfs*5 | Q9P2B7 | protein_coding | TCGA-AR-A0U0-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
CFAP97 | SNV | Missense_Mutation | rs373566490 | c.158N>T | p.Ser53Leu | p.S53L | Q9P2B7 | protein_coding | tolerated(0.61) | benign(0) | TCGA-FU-A3HZ-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
CFAP97 | SNV | Missense_Mutation | rs777547282 | c.1397N>A | p.Arg466His | p.R466H | Q9P2B7 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
CFAP97 | SNV | Missense_Mutation | c.775N>C | p.Ser259Pro | p.S259P | Q9P2B7 | protein_coding | deleterious(0) | probably_damaging(0.95) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
CFAP97 | SNV | Missense_Mutation | c.53N>G | p.Asp18Gly | p.D18G | Q9P2B7 | protein_coding | deleterious(0) | probably_damaging(0.984) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
CFAP97 | SNV | Missense_Mutation | novel | c.1069N>A | p.Asp357Asn | p.D357N | Q9P2B7 | protein_coding | tolerated(0.11) | probably_damaging(0.911) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
CFAP97 | SNV | Missense_Mutation | novel | c.495N>T | p.Lys165Asn | p.K165N | Q9P2B7 | protein_coding | deleterious(0.01) | benign(0.071) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
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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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