Abnormality Iris Morphology Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4025845
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Genes

27 genes associated with the disease Abnormality Iris Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTA2 actin, alpha 2, smooth muscle, aorta
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
ELN elastin
FBN1 fibrillin 1
FKRP fukutin related protein
FOXE3 forkhead box E3
GJA1 gap junction protein, alpha 1, 43kDa
GMPPB GDP-mannose pyrophosphorylase B
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
MYOC myocilin, trabecular meshwork inducible glucocorticoid response
PAX6 paired box 6
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
POMK protein-O-mannose kinase
POMT1 protein-O-mannosyltransferase 1
POMT2 protein-O-mannosyltransferase 2
PRKG1 protein kinase, cGMP-dependent, type I
PRR12 proline rich 12
SMAD3 SMAD family member 3
TBR1 T-box, brain, 1
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)