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Gene: COL14A1 |
Gene summary for COL14A1 |
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Gene information | Species | Human | Gene symbol | COL14A1 | Gene ID | 7373 |
Gene name | collagen type XIV alpha 1 chain | |
Gene Alias | UND | |
Cytomap | 8q24.12 | |
Gene Type | protein-coding | GO ID | GO:0007155 | UniProtAcc | Q05707 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
7373 | COL14A1 | cirrhotic3 | Human | Liver | Cirrhotic | 2.03e-08 | 3.31e-01 | 0.0215 |
7373 | COL14A1 | S014 | Human | Liver | HCC | 5.03e-06 | 5.23e-01 | 0.2254 |
7373 | COL14A1 | S015 | Human | Liver | HCC | 5.36e-09 | 7.74e-01 | 0.2375 |
7373 | COL14A1 | S016 | Human | Liver | HCC | 1.65e-04 | 5.45e-01 | 0.2243 |
7373 | COL14A1 | male-WTA | Human | Thyroid | PTC | 3.17e-68 | 8.45e-01 | 0.1037 |
7373 | COL14A1 | PTC01 | Human | Thyroid | PTC | 3.72e-16 | 3.45e-01 | 0.1899 |
7373 | COL14A1 | PTC04 | Human | Thyroid | PTC | 5.58e-09 | 6.32e-01 | 0.1927 |
7373 | COL14A1 | PTC05 | Human | Thyroid | PTC | 4.83e-07 | 7.27e-01 | 0.2065 |
7373 | COL14A1 | PTC06 | Human | Thyroid | PTC | 2.55e-51 | 1.96e+00 | 0.2057 |
7373 | COL14A1 | PTC07 | Human | Thyroid | PTC | 5.48e-60 | 1.32e+00 | 0.2044 |
7373 | COL14A1 | ATC13 | Human | Thyroid | ATC | 2.50e-70 | 2.60e+00 | 0.34 |
7373 | COL14A1 | ATC5 | Human | Thyroid | ATC | 4.04e-84 | 2.74e+00 | 0.34 |
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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:00301986 | Thyroid | PTC | extracellular matrix organization | 124/5968 | 301/18723 | 3.75e-04 | 2.53e-03 | 124 |
GO:00430626 | Thyroid | PTC | extracellular structure organization | 124/5968 | 302/18723 | 4.38e-04 | 2.92e-03 | 124 |
GO:00452296 | Thyroid | PTC | external encapsulating structure organization | 124/5968 | 304/18723 | 5.96e-04 | 3.79e-03 | 124 |
GO:00301995 | Thyroid | PTC | collagen fibril organization | 29/5968 | 61/18723 | 7.57e-03 | 3.23e-02 | 29 |
GO:003019812 | Thyroid | ATC | extracellular matrix organization | 152/6293 | 301/18723 | 8.63e-10 | 2.24e-08 | 152 |
GO:004306212 | Thyroid | ATC | extracellular structure organization | 152/6293 | 302/18723 | 1.17e-09 | 2.94e-08 | 152 |
GO:004522912 | Thyroid | ATC | external encapsulating structure organization | 152/6293 | 304/18723 | 2.11e-09 | 5.08e-08 | 152 |
GO:003019911 | Thyroid | ATC | collagen fibril organization | 43/6293 | 61/18723 | 4.24e-09 | 9.57e-08 | 43 |
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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 |
COL14A1 | SNV | Missense_Mutation | rs139519867 | c.1747G>A | p.Asp583Asn | p.D583N | Q05707 | protein_coding | tolerated(0.1) | possibly_damaging(0.805) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
COL14A1 | SNV | Missense_Mutation | rs563811899 | c.3415G>A | p.Val1139Met | p.V1139M | Q05707 | protein_coding | deleterious(0) | probably_damaging(0.979) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
COL14A1 | SNV | Missense_Mutation | c.3560G>A | p.Arg1187His | p.R1187H | Q05707 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
COL14A1 | SNV | Missense_Mutation | novel | c.3724G>T | p.Asp1242Tyr | p.D1242Y | Q05707 | protein_coding | deleterious(0.05) | benign(0.201) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
COL14A1 | SNV | Missense_Mutation | rs746931765 | c.4685C>T | p.Ser1562Leu | p.S1562L | Q05707 | protein_coding | tolerated(0.26) | benign(0.047) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
COL14A1 | SNV | Missense_Mutation | rs76456653 | c.2056G>A | p.Gly686Ser | p.G686S | Q05707 | protein_coding | tolerated(0.32) | benign(0.071) | TCGA-A5-A0VP-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
COL14A1 | SNV | Missense_Mutation | novel | c.4500G>T | p.Gln1500His | p.Q1500H | Q05707 | protein_coding | deleterious(0.02) | probably_damaging(0.996) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
COL14A1 | SNV | Missense_Mutation | rs763832906 | c.565G>A | p.Asp189Asn | p.D189N | Q05707 | protein_coding | tolerated(0.24) | benign(0) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
COL14A1 | SNV | Missense_Mutation | c.1697G>A | p.Arg566Gln | p.R566Q | Q05707 | protein_coding | deleterious(0.02) | possibly_damaging(0.834) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
COL14A1 | SNV | Missense_Mutation | novel | c.4577A>C | p.Lys1526Thr | p.K1526T | Q05707 | protein_coding | tolerated(0.09) | probably_damaging(0.989) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=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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