sudden infant death Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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Genes

23 genes associated with the disease sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ADCYAP1 adenylate cyclase activating polypeptide 1 (pituitary)
APOE apolipoprotein E
AQP4 aquaporin 4
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
FMO3 flavin containing monooxygenase 3
GSTT1 glutathione S-transferase theta 1
IL10 interleukin 10
IL1B interleukin 1, beta
IL1RN interleukin 1 receptor antagonist
IL6 interleukin 6
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
MAOA monoamine oxidase A
NOS1AP nitric oxide synthase 1 (neuronal) adaptor protein
SCN5A sodium channel, voltage gated, type V alpha subunit
SFTPA1 surfactant protein A1
SFTPA2 surfactant protein A2
SFTPD surfactant protein D
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TH tyrosine hydroxylase
TNF tumor necrosis factor
TPH2 tryptophan hydroxylase 2