Abnormal Globus Pallidus Morphology Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	any structural anomaly of one of the basal ganglia involved with control of voluntary movement in the brain; consists of an external and an internal segment (Mammalian Phenotype Ontology, MP_0004081)
External Link	https://www.disgenet.org/browser/0/1/0/C4025706
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Genes

10 genes associated with the disease Abnormal Globus Pallidus Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
C19ORF12	chromosome 19 open reading frame 12
CYP2U1	cytochrome P450, family 2, subfamily U, polypeptide 1
KCNQ2	potassium channel, voltage gated KQT-like subfamily Q, member 2
MMUT	methylmalonyl-CoA mutase
NDUFAF3	NADH dehydrogenase (ubiquinone) complex I, assembly factor 3
NDUFB8	NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 8, 19kDa
NDUFS2	NADH dehydrogenase (ubiquinone) Fe-S protein 2, 49kDa (NADH-coenzyme Q reductase)
SCO2	SCO2 cytochrome c oxidase assembly protein
SLC30A10	solute carrier family 30, member 10
SURF1	surfeit 1