abnormal nervous system electrophysiology Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the function of the electrical signals with which nerve cells communicate with each other or with muscles as measured by electrophysiological investigations. (Human Phenotype Ontology, HP_0001311)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0001311
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Genes

11 genes associated with the abnormal nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6 1.40373
SYT1 synaptotagmin I 1.30781
BICD1 bicaudal D homolog 1 (Drosophila) 1.24866
SGIP1 SH3-domain GRB2-like (endophilin) interacting protein 1 1.20773
UGDH UDP-glucose 6-dehydrogenase 1.16642
ST6GALNAC3 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 1.16497
LIAS lipoic acid synthetase 1.09266
RPL9 ribosomal protein L9 1.02775
ARHGAP8 Rho GTPase activating protein 8 0.969142
C11ORF84 chromosome 11 open reading frame 84 0.882984
FAM65B family with sequence similarity 65, member B 0.868241