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Gene: C16orf96 |
Gene summary for C16ORF96 |
Gene summary. |
Gene information | Species | Human | Gene symbol | C16orf96 | Gene ID | 342346 |
Gene name | chromosome 16 open reading frame 96 | |
Gene Alias | C16orf96 | |
Cytomap | 16p13.3 | |
Gene Type | protein-coding | GO ID | NA | UniProtAcc | A6NNT2 |
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Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
342346 | C16orf96 | HTA11_3410_2000001011 | Human | Colorectum | AD | 7.98e-03 | 9.20e-02 | 0.0155 |
342346 | C16orf96 | HTA11_2487_2000001011 | Human | Colorectum | SER | 8.42e-05 | 1.66e-01 | -0.1808 |
342346 | C16orf96 | HTA11_1938_2000001011 | Human | Colorectum | AD | 5.27e-05 | 1.81e-01 | -0.0811 |
342346 | C16orf96 | HTA11_78_2000001011 | Human | Colorectum | AD | 2.02e-04 | 1.63e-01 | -0.1088 |
342346 | C16orf96 | HTA11_347_2000001011 | Human | Colorectum | AD | 3.56e-12 | 2.60e-01 | -0.1954 |
342346 | C16orf96 | HTA11_411_2000001011 | Human | Colorectum | SER | 5.61e-03 | 2.88e-01 | -0.2602 |
342346 | C16orf96 | HTA11_3361_2000001011 | Human | Colorectum | AD | 2.22e-02 | 2.41e-01 | -0.1207 |
342346 | C16orf96 | HTA11_83_2000001011 | Human | Colorectum | SER | 3.64e-05 | 2.13e-01 | -0.1526 |
342346 | C16orf96 | HTA11_1391_2000001011 | Human | Colorectum | AD | 1.30e-10 | 2.80e-01 | -0.059 |
342346 | C16orf96 | HTA11_2992_2000001011 | Human | Colorectum | SER | 1.94e-06 | 2.82e-01 | -0.1706 |
342346 | C16orf96 | HTA11_5216_2000001011 | Human | Colorectum | SER | 3.34e-04 | 3.57e-01 | -0.1462 |
342346 | C16orf96 | HTA11_546_2000001011 | Human | Colorectum | AD | 1.44e-03 | 1.63e-01 | -0.0842 |
342346 | C16orf96 | HTA11_7862_2000001011 | Human | Colorectum | AD | 1.96e-03 | 1.74e-01 | -0.0179 |
342346 | C16orf96 | HTA11_866_3004761011 | Human | Colorectum | AD | 2.04e-08 | 2.06e-01 | 0.096 |
342346 | C16orf96 | HTA11_8622_2000001021 | Human | Colorectum | SER | 4.45e-03 | 2.21e-01 | 0.0528 |
342346 | C16orf96 | HTA11_6818_2000001021 | Human | Colorectum | AD | 2.93e-13 | 3.92e-01 | 0.0588 |
342346 | C16orf96 | HTA11_99999970781_79442 | Human | Colorectum | MSS | 9.34e-09 | 2.37e-01 | 0.294 |
342346 | C16orf96 | HTA11_99999965062_69753 | Human | Colorectum | MSI-H | 1.89e-11 | 8.82e-01 | 0.3487 |
342346 | C16orf96 | HTA11_99999971662_82457 | Human | Colorectum | MSS | 1.31e-09 | 3.06e-01 | 0.3859 |
342346 | C16orf96 | HTA11_99999973899_84307 | Human | Colorectum | MSS | 1.14e-04 | 1.79e-01 | 0.2585 |
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Transcriptomic changes along malignancy continuum. |
∗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 |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
Figure of enriched GO biological processes. |
Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | CRC | |
Stomach | GC | |
Stomach | CAG with IM | |
Stomach | CSG | |
Stomach | CAG |
∗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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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
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 |
Annotation of somatic variants for genes involved in malignant transformation |
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 |
C16orf96 | SNV | Missense_Mutation | novel | c.1628T>C | p.Val543Ala | p.V543A | A6NNT2 | protein_coding | tolerated(1) | benign(0) | TCGA-A2-A3KC-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD |
C16orf96 | SNV | Missense_Mutation | novel | c.248N>C | p.His83Pro | p.H83P | A6NNT2 | protein_coding | deleterious(0) | benign(0.05) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
C16orf96 | SNV | Missense_Mutation | novel | c.3365N>T | p.Arg1122Ile | p.R1122I | A6NNT2 | protein_coding | deleterious(0) | probably_damaging(0.943) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
C16orf96 | SNV | Missense_Mutation | c.544G>T | p.Asp182Tyr | p.D182Y | A6NNT2 | protein_coding | deleterious(0) | possibly_damaging(0.73) | TCGA-AO-A03T-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD | |
C16orf96 | SNV | Missense_Mutation | novel | c.2721N>G | p.Phe907Leu | p.F907L | A6NNT2 | protein_coding | deleterious(0.05) | probably_damaging(0.996) | TCGA-PE-A5DE-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | CR |
C16orf96 | SNV | Missense_Mutation | c.1324C>G | p.Gln442Glu | p.Q442E | A6NNT2 | protein_coding | tolerated(0.24) | benign(0.01) | TCGA-XX-A899-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cytoxan | CR | |
C16orf96 | deletion | Frame_Shift_Del | c.1242delG | p.Pro415GlnfsTer42 | p.P415Qfs*42 | A6NNT2 | protein_coding | TCGA-D8-A27V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | |||
C16orf96 | SNV | Missense_Mutation | novel | c.1408N>T | p.Arg470Trp | p.R470W | A6NNT2 | protein_coding | deleterious(0.01) | benign(0) | TCGA-MA-AA41-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
C16orf96 | SNV | Missense_Mutation | c.274N>A | p.Glu92Lys | p.E92K | A6NNT2 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-MU-A5YI-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | PD | |
C16orf96 | SNV | Missense_Mutation | c.2668N>C | p.Glu890Gln | p.E890Q | A6NNT2 | protein_coding | deleterious(0) | probably_damaging(0.984) | TCGA-Q1-A5R2-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | PR |
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Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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