Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3992
Gene Symbol: FADS1
FADS1
0.110 GeneticVariation disease BEFREE The fatty acid desaturase 1 (FADS1) gene variant is a novel susceptibility marker for laryngeal squamous cell carcinoma identified by a recent genome-wide association study, but it is still unclear whether this genetic variant continues to influence oral cancer recurrence or death. 27542551 2017
Entrez Id: 3992
Gene Symbol: FADS1
FADS1
0.110 GeneticVariation disease GWASCAT Genome-wide association study identifies three susceptibility loci for laryngeal squamous cell carcinoma in the Chinese population. 25194280 2014
Entrez Id: 595
Gene Symbol: CCND1
CCND1
0.100 GeneticVariation disease BEFREE Cyclin D1 A870G polymorphism and amplification in laryngeal squamous cell carcinoma: implications of tumor localization and tobacco exposure. 15350626 2004
Entrez Id: 1956
Gene Symbol: EGFR
EGFR
0.100 GeneticVariation disease BEFREE Evaluation of epidermal growth factor receptor gene and chromosome 7 alterations in squamous cell carcinoma of the larynx, using chromogenic in situ hybridization on tissue microarrays. 16882359 2007
Entrez Id: 595
Gene Symbol: CCND1
CCND1
0.100 GeneticVariation disease BEFREE Cyclin D1 gene (CCND1) polymorphism and the risk of squamous cell carcinoma of the larynx. 16258756 2006
Entrez Id: 1029
Gene Symbol: CDKN2A
CDKN2A
0.100 GeneticVariation disease BEFREE p16MTS1/CDK4I mutations and concomitant loss of heterozygosity at 9p21-23 are frequent events in squamous cell carcinoma of the larynx. 9333020 1997
Entrez Id: 1956
Gene Symbol: EGFR
EGFR
0.100 GeneticVariation disease BEFREE Tissue microarray analysis of EGFR and HER2 oncogene copy number alterations in squamous cell carcinoma of the larynx. 15592685 2005
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.100 GeneticVariation disease BEFREE High frequency of p53 gene alterations associated with protein overexpression in human squamous cell carcinoma of the larynx. 1594246 1992
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.100 GeneticVariation disease BEFREE We have analyzed by immunohistochemistry p21 and p27 expression in a series of 132 patients who underwent surgical resection of their LSCC and who had previously been investigated for p53 gene mutations and cyclin D1 expression. 10506612 1999
Entrez Id: 595
Gene Symbol: CCND1
CCND1
0.100 GeneticVariation disease BEFREE We have analyzed by immunohistochemistry p21 and p27 expression in a series of 132 patients who underwent surgical resection of their LSCC and who had previously been investigated for p53 gene mutations and cyclin D1 expression. 10506612 1999
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.100 GeneticVariation disease BEFREE TP53 mutations and S-phase fraction but not DNA-ploidy are independent prognostic indicators in laryngeal squamous cell carcinoma. 15965904 2006
Entrez Id: 1956
Gene Symbol: EGFR
EGFR
0.100 GeneticVariation disease BEFREE Clinical significance of KRAS gene mutation and epidermal growth factor receptor expression in Japanese patients with squamous cell carcinoma of the larynx, oropharynx and hypopharynx. 22441881 2013
Entrez Id: 1956
Gene Symbol: EGFR
EGFR
0.100 GeneticVariation disease BEFREE Two LSCC specimens were positive for EGFR exon 21 mutation (1.52%).The mutation was p.L858R in exon 21. 24646139 2014
Entrez Id: 9415
Gene Symbol: FADS2
FADS2
0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies three susceptibility loci for laryngeal squamous cell carcinoma in the Chinese population. 25194280 2014
Entrez Id: 1462
Gene Symbol: VCAN
VCAN
0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies three susceptibility loci for laryngeal squamous cell carcinoma in the Chinese population. 25194280 2014
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.100 GeneticVariation disease BEFREE To investigate the p53 and O<sup>6</sup>-methylguanine DNA methyltransferase (MGMT)5' upstream sequence gene promoter regions for single nucleotide polymorphisms and explore the p53 gene 5' upstream sequence consisting of two haplotypes to provide a genetic marker for the incidence of laryngeal squamous cell carcinoma. 28739733 2017
Entrez Id: 7157
Gene Symbol: TP53
TP53
0.100 GeneticVariation disease BEFREE Seventeen of 19 (84.2%) cases showing p53 gene mutations were stage III and IV, which suggests that p53 gene mutation is a rather late event in tumor development and is involved in the progression of laryngeal squamous cell carcinoma. 8866234 1996
Entrez Id: 261
Gene Symbol: AMCN
AMCN
0.080 GeneticVariation disease BEFREE Suppressing SNHG12 using siRNA inhibited proliferation and invasion and promoted apoptosis in the AMC-HN-8 LSCC cell line. 31348766 2019
Entrez Id: 5290
Gene Symbol: PIK3CA
PIK3CA
0.060 GeneticVariation disease BEFREE Mutations in PIK3CA and FGFR3 were detected in PD and LSCC cases, as well as other HNSCC cases, but absent in NPD cases. 29700339 2018
Entrez Id: 27306
Gene Symbol: HPGDS
HPGDS
0.040 GeneticVariation disease BEFREE To investigate the influence of the glutathione S-transferase (GST) M1, T1, and P1 genotypes on the laryngeal squamous cell carcinoma risk. 15334395 2005
Entrez Id: 27306
Gene Symbol: HPGDS
HPGDS
0.040 GeneticVariation disease BEFREE Genetic deletions of glutathione-S-transferase as a risk factor in squamous cell carcinoma of the larynx: a preliminary report. 11283827 2001
Entrez Id: 27306
Gene Symbol: HPGDS
HPGDS
0.040 GeneticVariation disease BEFREE Glutathione S-transferase and cytochrome-P-450 polymorphism as risk factors for squamous cell carcinoma of the larynx. 8988674 1996
Entrez Id: 6279
Gene Symbol: S100A8
S100A8
0.040 GeneticVariation disease BEFREE UreA and cagA genes of Helicobacter pylori in Egyptian patients with laryngeal squamous cell carcinoma and benign laryngeal polyps: a cohort study. 27225283 2016
Entrez Id: 1030
Gene Symbol: CDKN2B
CDKN2B
0.040 GeneticVariation disease BEFREE p16MTS1/CDK4I mutations and concomitant loss of heterozygosity at 9p21-23 are frequent events in squamous cell carcinoma of the larynx. 9333020 1997
Entrez Id: 6790
Gene Symbol: AURKA
AURKA
0.040 GeneticVariation disease BEFREE To investigate the role of STK15 gene abnormalities in the occurrence of centrosomal amplification and chromosomal instability, a combinatory approach has been taken to investigate the expression level and point mutations of the STK15 and centrosomal/chromosomal aberrations among 72 cases of laryngeal squamous cell carcinoma and a representative Hep-2 cell line. 16377583 2005