abnormality of central nervous system electrophysiology Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0030178
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Genes

11 genes associated with the abnormality of central 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