abnormality of vision evoked potentials Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of visually evoked potentials (VEP), which are electrical potentials, initiated by brief visual stimuli, which are recorded from the scalp overlying the visual cortex. (Human Phenotype Ontology, HP_0000649)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000649
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Genes

42 genes associated with the abnormality of vision evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia
ACOX1 acyl-CoA oxidase 1, palmitoyl
ASPA aspartoacylase
CLCN7 chloride channel, voltage-sensitive 7
COX1
COX2
COX3
ELOVL4 ELOVL fatty acid elongase 4
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
FXN frataxin
GALC galactosylceramidase
MFN2 mitofusin 2
MT-ND4 NADH dehydrogenase, subunit 4 (complex I)
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
MT-TF tRNA
MT-TH tRNA
MT-TL1 tRNA
MT-TQ tRNA
MT-TS1 tRNA
MT-TS2 tRNA
MT-TW tRNA
ND1
NDRG1 N-myc downstream regulated 1
NOTCH3 notch 3
OPA1 optic atrophy 1 (autosomal dominant)
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
POLG polymerase (DNA directed), gamma
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
RAB18 RAB18, member RAS oncogene family
RAB3GAP1 RAB3 GTPase activating protein subunit 1 (catalytic)
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic)
SLC25A22 solute carrier family 25 (mitochondrial carrier: glutamate), member 22
SNX10 sorting nexin 10
SUCLA2 succinate-CoA ligase, ADP-forming, beta subunit
TBC1D20 TBC1 domain family, member 20
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
TTPA tocopherol (alpha) transfer protein
TYR tyrosinase
WFS1 Wolfram syndrome 1 (wolframin)