abolished electroretinogram (erg) Gene Set
Genes
18 genes associated with the abolished electroretinogram (erg) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
CLN3
|
ceroid-lipofuscinosis, neuronal 3
|
|
CRB1
|
crumbs family member 1, photoreceptor morphogenesis associated
|
|
CRX
|
cone-rod homeobox
|
|
EYS
|
eyes shut homolog (Drosophila)
|
|
FLVCR1
|
feline leukemia virus subgroup C cellular receptor 1
|
|
HSD17B4
|
hydroxysteroid (17-beta) dehydrogenase 4
|
|
LCA5
|
Leber congenital amaurosis 5
|
|
LRAT
|
lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
|
|
MYO7A
|
myosin VIIA
|
|
NR2E3
|
nuclear receptor subfamily 2, group E, member 3
|
|
NRL
|
neural retina leucine zipper
|
|
PDE6D
|
phosphodiesterase 6D, cGMP-specific, rod, delta
|
|
POMGNT1
|
protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
|
|
PPT1
|
palmitoyl-protein thioesterase 1
|
|
PRCD
|
progressive rod-cone degeneration
|
|
PROM1
|
prominin 1
|
|
RPGRIP1
|
retinitis pigmentosa GTPase regulator interacting protein 1
|
|
TPP1
|
tripeptidyl peptidase I
|
