disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. (Human Disease Ontology, DOID_4)
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16 genes associated with the disease disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
AGMAT agmatine ureohydrolase (agmatinase)
CCDC91 coiled-coil domain containing 91
GSTT1 glutathione S-transferase theta 1
HLA-B major histocompatibility complex, class I, B
INPP5B inositol polyphosphate-5-phosphatase, 75kDa
MARC2 mitochondrial amidoxime reducing component 2
MMP2 matrix metallopeptidase 2
MMP9 matrix metallopeptidase 9
NRAP nebulin-related anchoring protein
OVOS2 ovostatin 2
PDPR pyruvate dehydrogenase phosphatase regulatory subunit
PTPRD protein tyrosine phosphatase, receptor type, D
TAF3 TAF3 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 140kDa
THSD7A thrombospondin, type I, domain containing 7A
TNNI3K TNNI3 interacting kinase
TTN titin