Male infertility
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
ELOVL2 controls the level of n-6 28:5 and 30:5 fatty acids in testis, a prerequisite for male fertility and sperm maturation in mice.
|
21106902 |
2011 |
Subfertility, Male
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
ELOVL2 controls the level of n-6 28:5 and 30:5 fatty acids in testis, a prerequisite for male fertility and sperm maturation in mice.
|
21106902 |
2011 |
Male sterility
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
ELOVL2 controls the level of n-6 28:5 and 30:5 fatty acids in testis, a prerequisite for male fertility and sperm maturation in mice.
|
21106902 |
2011 |
Phospholipid measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.
|
21829377 |
2011 |
Glucose measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Human metabolic individuality in biomedical and pharmaceutical research.
|
21886157 |
2011 |
elevated blood glucose level
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Human metabolic individuality in biomedical and pharmaceutical research.
|
21886157 |
2011 |
Coronary Artery Disease
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
To investigate the association between the polymorphisms of fatty acid desaturase 1 (FADS1), fatty acid desaturase 2 (FADS2) and elongation of very long chain fatty acids like 2 (ELOVL2) gene and coronary artery disease (CAD) in a Chinese Han population.
|
21917437 |
2011 |
Myocardial Infarction
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Variation in ELOVL2, ELOVL4 and ELOVL5 was not associated with adipose tissue fatty acids, intermediate cardiovascular risk factors or MI.
|
22293571 |
2012 |
Phospholipid measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
|
22359512 |
2012 |
Phospholipid measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
|
22359512 |
2012 |
Calcification of coronary artery
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.
|
22916037 |
2012 |
Liver carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The validation for the microarray was done by real time PCR assay in which PPP3CA, ATG-5, BACE genes showed down-regulation and ABCG2, RXRA, ELOVL2, CXR3 genes showed up-regulation. cDNA microarrays showed that among the major upregulated genes in HCC are sets.
|
23317196 |
2012 |
Acute Chest Syndrome
|
0.010 |
Biomarker
|
disease |
BEFREE |
The purpose of this study is to analyze the relationship between the polymorphisms of fatty acid desaturase 1 (FADS1), fatty acid desaturase 2 (FADS2), and elongation of very long-chain fatty acids-like 2 (ELOVL2) and acute coronary syndrome (ACS) in Chinese Han population.
|
23555103 |
2013 |
Acute Coronary Syndrome
|
0.010 |
Biomarker
|
disease |
BEFREE |
The purpose of this study is to analyze the relationship between the polymorphisms of fatty acid desaturase 1 (FADS1), fatty acid desaturase 2 (FADS2), and elongation of very long-chain fatty acids-like 2 (ELOVL2) and acute coronary syndrome (ACS) in Chinese Han population.
|
23555103 |
2013 |
Fatty acid measurement
|
0.100 |
GeneticVariation
|
group |
GWASCAT |
A genome-wide association study of saturated, mono- and polyunsaturated red blood cell fatty acids in the Framingham Heart Offspring Study.
|
25500335 |
2015 |
Non-alcoholic Fatty Liver Disease
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
These findings indicate that neonatal testosterone treatment, but not estradiol, produces histological changes in female rat liver that mimic NAFLD with testosterone-treated rats showing impaired BCAA metabolism and dysfunctions in ELOVL2, SLC22A4 and SLC16A9 activity.
|
29030588 |
2017 |
Kidney Failure, Chronic
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.
|
29545352 |
2018 |
Chronic Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
GWASCAT |
Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.
|
29545352 |
2018 |
Autism Spectrum Disorders
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
These findings provide evidence of an association between FADS2 and ELOVL2 polymorphisms and ASD susceptibility in Chinese children.
|
30180836 |
2018 |
Adverse effects, not elsewhere classified
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records.
|
30420678 |
2019 |
melanoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Genetic variants in ELOVL2 and HSD17B12 predict melanoma-specific survival.
|
30734280 |
2019 |
Glioblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Targeting ELOVL2 inhibited glioblastoma cell growth and tumor initiation.
|
31201181 |
2019 |
Adult Glioblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Targeting ELOVL2 inhibited glioblastoma cell growth and tumor initiation.
|
31201181 |
2019 |
Childhood Glioblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Targeting ELOVL2 inhibited glioblastoma cell growth and tumor initiation.
|
31201181 |
2019 |
Glioblastoma Multiforme
|
0.020 |
Biomarker
|
disease |
BEFREE |
Targeting ELOVL2 inhibited glioblastoma cell growth and tumor initiation.
|
31201181 |
2019 |