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Gene: SYNC |
Gene summary for SYNC |
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Gene information | Species | Human | Gene symbol | SYNC | Gene ID | 81493 |
Gene name | syncoilin, intermediate filament protein | |
Gene Alias | SYNC1 | |
Cytomap | 1p35.1 | |
Gene Type | protein-coding | GO ID | GO:0008150 | UniProtAcc | Q9H7C4 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
81493 | SYNC | LZE4T | Human | Esophagus | ESCC | 2.17e-07 | 2.43e-01 | 0.0811 |
81493 | SYNC | LZE5T | Human | Esophagus | ESCC | 1.55e-04 | 4.48e-01 | 0.0514 |
81493 | SYNC | LZE7T | Human | Esophagus | ESCC | 1.96e-16 | 1.00e+00 | 0.0667 |
81493 | SYNC | LZE8T | Human | Esophagus | ESCC | 2.34e-05 | 2.78e-01 | 0.067 |
81493 | SYNC | LZE20T | Human | Esophagus | ESCC | 2.20e-08 | 2.94e-01 | 0.0662 |
81493 | SYNC | LZE22T | Human | Esophagus | ESCC | 1.18e-10 | 6.34e-01 | 0.068 |
81493 | SYNC | LZE24T | Human | Esophagus | ESCC | 1.06e-22 | 6.11e-01 | 0.0596 |
81493 | SYNC | LZE6T | Human | Esophagus | ESCC | 2.09e-09 | 3.93e-01 | 0.0845 |
81493 | SYNC | P2T-E | Human | Esophagus | ESCC | 1.08e-05 | 1.03e-01 | 0.1177 |
81493 | SYNC | P10T-E | Human | Esophagus | ESCC | 3.29e-13 | 2.17e-01 | 0.116 |
81493 | SYNC | P16T-E | Human | Esophagus | ESCC | 1.88e-02 | 3.11e-02 | 0.1153 |
81493 | SYNC | P21T-E | Human | Esophagus | ESCC | 1.50e-03 | 9.06e-02 | 0.1617 |
81493 | SYNC | P57T-E | Human | Esophagus | ESCC | 1.22e-05 | 4.68e-02 | 0.0926 |
81493 | SYNC | P79T-E | Human | Esophagus | ESCC | 2.86e-05 | 4.35e-02 | 0.1154 |
81493 | SYNC | P130T-E | Human | Esophagus | ESCC | 5.72e-19 | 2.99e-01 | 0.1676 |
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Tissue | Expression Dynamics | Abbreviation |
Esophagus | ![]() | ESCC: Esophageal squamous cell carcinoma |
HGIN: High-grade intraepithelial neoplasias | ||
LGIN: Low-grade intraepithelial neoplasias |
∗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:000640124 | Oral cavity | EOLP | RNA catabolic process | 77/2218 | 278/18723 | 3.92e-13 | 1.12e-10 | 77 |
GO:000641726 | Oral cavity | EOLP | regulation of translation | 108/2218 | 468/18723 | 4.04e-12 | 7.34e-10 | 108 |
GO:004348823 | Oral cavity | EOLP | regulation of mRNA stability | 50/2218 | 158/18723 | 2.91e-11 | 4.15e-09 | 50 |
GO:000037725 | Oral cavity | EOLP | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 80/2218 | 320/18723 | 4.20e-11 | 5.60e-09 | 80 |
GO:000039825 | Oral cavity | EOLP | mRNA splicing, via spliceosome | 80/2218 | 320/18723 | 4.20e-11 | 5.60e-09 | 80 |
GO:000037525 | Oral cavity | EOLP | RNA splicing, via transesterification reactions | 80/2218 | 324/18723 | 8.11e-11 | 9.53e-09 | 80 |
GO:004348723 | Oral cavity | EOLP | regulation of RNA stability | 51/2218 | 170/18723 | 1.63e-10 | 1.68e-08 | 51 |
GO:003465523 | Oral cavity | EOLP | nucleobase-containing compound catabolic process | 89/2218 | 407/18723 | 5.47e-09 | 2.92e-07 | 89 |
GO:003133025 | Oral cavity | EOLP | negative regulation of cellular catabolic process | 64/2218 | 262/18723 | 9.72e-09 | 4.77e-07 | 64 |
GO:000989525 | Oral cavity | EOLP | negative regulation of catabolic process | 73/2218 | 320/18723 | 2.07e-08 | 8.84e-07 | 73 |
GO:004670023 | Oral cavity | EOLP | heterocycle catabolic process | 93/2218 | 445/18723 | 2.61e-08 | 1.08e-06 | 93 |
GO:190331225 | Oral cavity | EOLP | negative regulation of mRNA metabolic process | 31/2218 | 92/18723 | 3.14e-08 | 1.24e-06 | 31 |
GO:004427023 | Oral cavity | EOLP | cellular nitrogen compound catabolic process | 92/2218 | 451/18723 | 1.01e-07 | 3.45e-06 | 92 |
GO:001943923 | Oral cavity | EOLP | aromatic compound catabolic process | 92/2218 | 467/18723 | 5.23e-07 | 1.40e-05 | 92 |
GO:190136123 | Oral cavity | EOLP | organic cyclic compound catabolic process | 95/2218 | 495/18723 | 1.15e-06 | 2.80e-05 | 95 |
GO:190237310 | Oral cavity | EOLP | negative regulation of mRNA catabolic process | 22/2218 | 63/18723 | 1.55e-06 | 3.65e-05 | 22 |
GO:190236922 | Oral cavity | EOLP | negative regulation of RNA catabolic process | 24/2218 | 75/18723 | 3.13e-06 | 6.80e-05 | 24 |
GO:001714813 | Oral cavity | EOLP | negative regulation of translation | 54/2218 | 245/18723 | 4.15e-06 | 8.72e-05 | 54 |
GO:003434121 | Oral cavity | EOLP | response to interferon-gamma | 36/2218 | 141/18723 | 5.44e-06 | 1.08e-04 | 36 |
GO:003424913 | Oral cavity | EOLP | negative regulation of cellular amide metabolic process | 58/2218 | 273/18723 | 6.23e-06 | 1.22e-04 | 58 |
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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 |
SYNC | SNV | Missense_Mutation | c.809N>C | p.Phe270Ser | p.F270S | Q9H7C4 | protein_coding | tolerated(0.19) | probably_damaging(0.977) | TCGA-A6-3809-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
SYNC | SNV | Missense_Mutation | c.1193T>C | p.Leu398Pro | p.L398P | Q9H7C4 | protein_coding | deleterious(0) | probably_damaging(0.993) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
SYNC | SNV | Missense_Mutation | novel | c.1120N>A | p.Ala374Thr | p.A374T | Q9H7C4 | protein_coding | tolerated(0.14) | benign(0.053) | TCGA-AA-3947-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
SYNC | SNV | Missense_Mutation | c.1090N>G | p.Thr364Ala | p.T364A | Q9H7C4 | protein_coding | tolerated(0.26) | possibly_damaging(0.642) | TCGA-AA-A01P-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD | |
SYNC | SNV | Missense_Mutation | c.611N>A | p.Arg204Gln | p.R204Q | Q9H7C4 | protein_coding | tolerated(0.1) | probably_damaging(0.998) | TCGA-AD-A5EJ-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
SYNC | SNV | Missense_Mutation | rs763587503 | c.472G>A | p.Glu158Lys | p.E158K | Q9H7C4 | protein_coding | tolerated(0.77) | benign(0) | TCGA-AG-3591-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | I/II | Unspecific | Complete Response | |
SYNC | SNV | Missense_Mutation | novel | c.1116G>T | p.Lys372Asn | p.K372N | Q9H7C4 | protein_coding | deleterious(0) | possibly_damaging(0.864) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
SYNC | SNV | Missense_Mutation | c.418G>A | p.Gly140Arg | p.G140R | Q9H7C4 | protein_coding | tolerated_low_confidence(0.13) | benign(0.01) | TCGA-EI-6507-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
SYNC | SNV | Missense_Mutation | novel | c.1337C>T | p.Ala446Val | p.A446V | Q9H7C4 | protein_coding | tolerated(0.12) | possibly_damaging(0.698) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
SYNC | SNV | Missense_Mutation | novel | c.807G>T | p.Gln269His | p.Q269H | Q9H7C4 | protein_coding | deleterious(0.02) | probably_damaging(0.988) | TCGA-A5-A1OF-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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