Prenatal Maternal Abnormality Gene Set
Genes
22 genes associated with the disease Prenatal Maternal Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACTA2
|
actin, alpha 2, smooth muscle, aorta
|
|
CPT1A
|
carnitine palmitoyltransferase 1A (liver)
|
|
ELN
|
elastin
|
|
FBN1
|
fibrillin 1
|
|
FOXE3
|
forkhead box E3
|
|
HADHA
|
hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
|
|
HADHB
|
hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit
|
|
KCNMA1
|
potassium channel, calcium activated large conductance subfamily M alpha, member 1
|
|
LOX
|
lysyl oxidase
|
|
MAT2A
|
methionine adenosyltransferase II, alpha
|
|
MFAP5
|
microfibrillar associated protein 5
|
|
MYH11
|
myosin, heavy chain 11, smooth muscle
|
|
MYLK
|
myosin light chain kinase
|
|
PAH
|
phenylalanine hydroxylase
|
|
PRKG1
|
protein kinase, cGMP-dependent, type I
|
|
PURA
|
purine-rich element binding protein A
|
|
SLC35A2
|
solute carrier family 35 (UDP-galactose transporter), member A2
|
|
SMAD3
|
SMAD family member 3
|
|
TGFB2
|
transforming growth factor, beta 2
|
|
TGFB3
|
transforming growth factor, beta 3
|
|
TGFBR1
|
transforming growth factor, beta receptor 1
|
|
TGFBR2
|
transforming growth factor, beta receptor II (70/80kDa)
|
