ELAVL4, ELAV like RNA binding protein 4, 1996

N. diseases: 31; N. variants: 6
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023186
Disease: Learning Disorders
Learning Disorders
0.200 Biomarker group RGD PKC activation during training restores mushroom spine synapses and memory in the aged rat. 23545166 2013
CUI: C0751265
Disease: Learning Disabilities
Learning Disabilities
0.200 Biomarker disease RGD PKC activation during training restores mushroom spine synapses and memory in the aged rat. 23545166 2013
CUI: C0038220
Disease: Status Epilepticus
Status Epilepticus
0.200 Biomarker disease RGD Coordinated expression of HuD and GAP-43 in hippocampal dentate granule cells during developmental and adult plasticity. 17577668 2007
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.200 Biomarker disease RGD Neuronal HuD gene encoding a mRNA stability regulator is transcriptionally repressed by thyroid hormone. 12859688 2003
CUI: C0149940
Disease: Sciatic Neuropathy
Sciatic Neuropathy
0.200 Biomarker disease RGD Increased expression and localization of the RNA-binding protein HuD and GAP-43 mRNA to cytoplasmic granules in DRG neurons during nerve regeneration. 12957493 2003
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation disease GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
CUI: C0037369
Disease: Smoking
Smoking
0.100 GeneticVariation phenotype GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.100 GeneticVariation disease GWASCAT Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions. 30718901 2019
CUI: C1305855
Disease: Body mass index
Body mass index
0.100 GeneticVariation phenotype GWASCAT A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. 30108127 2018
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 GeneticVariation disease GWASCAT Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. 28991256 2017
CUI: C1305855
Disease: Body mass index
Body mass index
0.100 GeneticVariation phenotype GWASCAT The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. 26426971 2015
CUI: C1305855
Disease: Body mass index
Body mass index
0.100 GeneticVariation phenotype GWASCAT Genetic studies of body mass index yield new insights for obesity biology. 25673413 2015
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.060 Biomarker disease BEFREE The aim of this study was to investigate the serum HuD concentration in SCLC patients and the possibility of its utilization as a biomarker of small cell lung cancer. 28739747 2017
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.060 Biomarker disease BEFREE Specifically, the N-terminal region of ELAVL4, previously implicated in SCLC-associated autoimmunity, undergoes isoaspartylation in vitro, is recognized by sera from anti-ELAVL4 positive SCLC patients and is highly immunogenic in subcutaneously injected mice and in vitro stimulated human lymphocytes. 27725125 2016
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.060 AlteredExpression disease LHGDN Molecular detection of neuron-specific ELAV-like-positive cells in the peripheral blood of patients with small-cell lung cancer. 18607064 2008
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.060 AlteredExpression disease BEFREE Anti-Hu syndrome is a paraneoplastic neurologic disease seemingly associated with an efficient antitumoral immune response against HuD protein expressed by both small cell lung cancer (SCLC) and neurons. 14512168 2003
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.060 AlteredExpression disease BEFREE These results revealed that no aberrant alternative splicing occurred in SCLC not associated with PEM/PSN and the expression of HuD gene was not specific for a particular histologic subtype of human lung cancer. 9288629 1997
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.060 AlteredExpression disease BEFREE These results show that the HuD gene is not mutated in lung cancer, including tumors from patients producing anti-HuD antibodies, but HuD expression is an independent marker or determinant of the neuroendocrine differentiation seen in SCLC. 8069866 1994
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.040 Biomarker disease BEFREE Previous studies indicate that as many as six genes within the PARK10 region (RNF11, UQCRH, HIVEP3, EIF2B3, USP24, ELAVL4) might modify susceptibility or age at onset in Parkinson's disease (PD). 24156912 2014
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.040 Biomarker disease LHGDN This replication of association with rs967582 in a third cohort further implicates ELAVL4 as a PD susceptibility gene. 18587682 2008
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.040 GeneticVariation disease BEFREE This replication of association with rs967582 in a third cohort further implicates ELAVL4 as a PD susceptibility gene. 18587682 2008
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.040 Biomarker disease BEFREE Our data suggest that the association between ELAVL4 and PD previously observed might be explained by a Celtic-founder effect. 17230446 2007
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.040 Biomarker disease LHGDN SNP 2 (located in the first intron of ELAVL4) showed a strong significant association with AAO of PD (P = 0.006), and SNP 5 (a coding SNP in ELAVL4) showed a moderately significant association (P = 0.035). 15827745 2005
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.040 Biomarker disease BEFREE SNP 2 (located in the first intron of ELAVL4) showed a strong significant association with AAO of PD (P = 0.006), and SNP 5 (a coding SNP in ELAVL4) showed a moderately significant association (P = 0.035). 15827745 2005
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.030 GeneticVariation disease BEFREE Molecular analysis of the HuD gene in neuroendocrine lung cancers. 19410329 2010