sids/sudden infant death syndrome Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group unknown (Genetic Association Database)
Similar Terms
Downloads & Tools


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

Symbol Name
ASCL1 achaete-scute family bHLH transcription factor 1
BMP2 bone morphogenetic protein 2
ECE1 endothelin converting enzyme 1
EDN1 endothelin 1
EN1 engrailed homeobox 1
G6PC glucose-6-phosphatase, catalytic subunit
GCK glucokinase (hexokinase 4)
PHOX2A paired-like homeobox 2a
PHOX2B paired-like homeobox 2b
RET ret proto-oncogene
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TLX3 T-cell leukemia homeobox 3