PLA2G6, phospholipase A2 group VI, 8398

N. diseases: 350; N. variants: 102
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025202
Disease: melanoma
melanoma
0.170 GeneticVariation disease BEFREE Amelanotic/hypomelanotic melanoma was associated with TYR rs1126809*A/A [OR (CI 95%) 2.7 (1.1-6.8) vs. 1.2 (0.8-1.9)] and PLA2G6 rs11570734*A/A [OR (CI 95%) 3.7 (1.0-13.6) vs. 1.3 (0.9-2.0)]. 30680790 2019
CUI: C0025202
Disease: melanoma
melanoma
0.170 GeneticVariation disease BEFREE PLA2G6 rs132985*T was associated with BRAF V600E (OR = 1.32, 95% CI = 1.05-1.67) and BRAF other (OR = 1.82, 95% CI = 1.11-2.98), but not BRAF V600K or NRAS+ melanoma. 29753029 2018
CUI: C0025202
Disease: melanoma
melanoma
0.170 GeneticVariation disease BEFREE In addition, we show that skin DNA methylation is associated in cis with known genome-wide association study single nucleotide polymorphisms for nevus count, at PLA2G6 (P = 1.7 × 10<sup>-49</sup>) and NID1 (P = 6.4 × 10<sup>-14</sup>), as well as melanoma risk, including in or near MC1R, MX2, and TERT/CLPTM1L (P < 1 × 10<sup>-10</sup>). 27993549 2017
CUI: C0025202
Disease: melanoma
melanoma
0.170 GeneticVariation disease GWASCAT Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma. 28212542 2017
CUI: C0025202
Disease: melanoma
melanoma
0.170 GeneticVariation disease BEFREE The risk associations with 16 SNPs around DUSP14 (rs1051849) and a previous reported melanoma locus MAFF/PLA2G6 (proxy SNP rs4608623) were replicated in the GenoMEL dataset (P < 0.01) but failed in the Australian dataset. 23291271 2013
CUI: C0025202
Disease: melanoma
melanoma
0.170 GeneticVariation disease GWASDB A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. 21706340 2012
CUI: C0025202
Disease: melanoma
melanoma
0.170 Biomarker disease BEFREE A series of genome-wide association studies (GWASs) in 2008 and 2009 showed that a handful of additional genes (e.g., ASIP, TYR, and PLA2G6) influencing these endophenotypes also affected melanoma risk. 22475760 2012
CUI: C0025202
Disease: melanoma
melanoma
0.170 Biomarker disease BEFREE We genotyped 1028 invasive case patients and 1469 controls for variants in methylthioadenosine phosphorylase (MTAP), phospholipase A2, group VI (PLA2G6), and Interferon regulatory factor 4 (IRF4), and compared allelic frequencies globally and by anatomical site and histological subtype of melanoma. 21962134 2011
CUI: C0025202
Disease: melanoma
melanoma
0.170 AlteredExpression disease BEFREE In immortalized rat brain GP8.3 EC cultures, conditioned media (CM) prepared from SK-MEL28 and OCM-1 melanoma cells significantly enhanced arachidonic acid release, cytosolic phospholipase A(2) (cPLA(2)) and Ca(+)-independent phospholipase A(2) (iPLA(2)) specific activities, and cell growth by 24 h. Inhibitors such as wortmannin and LY294002 (vs. PI3 kinase activity), AACOCF(3), (vs. cPLA(2) and iPLA(2)), PD98059 (vs. ERK1/2 activity) and NS-398 (vs. cyclooxygenase-2 activity, COX-2) were all able to block cell proliferation and motility determined using a scratch wound healing assay in melanoma CMs-stimulated EC monolayers. 19747926 2009
CUI: C0025202
Disease: melanoma
melanoma
0.170 GeneticVariation disease GWASCAT Genome-wide association study identifies three loci associated with melanoma risk. 19578364 2009
CUI: C0025202
Disease: melanoma
melanoma
0.170 GeneticVariation disease GWASDB Genome-wide association study identifies three loci associated with melanoma risk. 19578364 2009