abnormality of the vasculature of the conjunctiva Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the blood vessels of the conjunctiva. (Human Phenotype Ontology, HP_0008054)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008054
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Genes

13 genes associated with the abnormality of the vasculature of the conjunctiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACVRL1 activin A receptor type II-like 1
ATM ATM serine/threonine kinase
CTSA cathepsin A
ENG endoglin
FUCA1 fucosidase, alpha-L- 1, tissue
GDF2 growth differentiation factor 2
GLA galactosidase, alpha
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
MANBA mannosidase, beta A, lysosomal
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
PCNA proliferating cell nuclear antigen
SETX senataxin
SMAD4 SMAD family member 4