natriuretic peptide, brain Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group neurological (Genetic Association Database)
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17 genes associated with the disease natriuretic peptide, brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CCDC180 coiled-coil domain containing 180
CHRM3 cholinergic receptor, muscarinic 3
CLCN6 chloride channel, voltage-sensitive 6
DECR1 2,4-dienoyl CoA reductase 1, mitochondrial
DISC1 disrupted in schizophrenia 1
EFNB2 ephrin-B2
ITGBL1 integrin, beta-like 1 (with EGF-like repeat domains)
KALRN kalirin, RhoGEF kinase
KAT6B K(lysine) acetyltransferase 6B
KCNIP4 Kv channel interacting protein 4
KIAA1324 KIAA1324
MYRIP myosin VIIA and Rab interacting protein
NAALADL2 N-acetylated alpha-linked acidic dipeptidase-like 2
NBN nibrin
NCAM1 neural cell adhesion molecule 1
NFIA nuclear factor I/A
ST18 suppression of tumorigenicity 18, zinc finger