Abnormal Saccadic Eye Movement Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0234649
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Genes

17 genes associated with the disease Abnormal Saccadic Eye Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
C19ORF12 chromosome 19 open reading frame 12
CSF1R colony stimulating factor 1 receptor
FXN frataxin
GBA2 glucosidase, beta (bile acid) 2
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
KIF1A kinesin family member 1A
MAPT microtubule-associated protein tau
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)
PNKP polynucleotide kinase 3'-phosphatase
SCO2 SCO2 cytochrome c oxidase assembly protein
SCP2 sterol carrier protein 2
SURF1 surfeit 1
TMEM216 transmembrane protein 216
TUBB3 tubulin, beta 3 class III