Obsolete Rod-Cone Dystrophy Gene Set
Genes
28 genes associated with the disease Obsolete Rod-Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ABHD12
|
abhydrolase domain containing 12
|
|
ALMS1
|
Alstrom syndrome protein 1
|
|
BBS1
|
Bardet-Biedl syndrome 1
|
|
BBS2
|
Bardet-Biedl syndrome 2
|
|
C2ORF71
|
chromosome 2 open reading frame 71
|
|
CEP19
|
centrosomal protein 19kDa
|
|
CLRN1
|
clarin 1
|
|
CNGA1
|
cyclic nucleotide gated channel alpha 1
|
|
CNGA3
|
cyclic nucleotide gated channel alpha 3
|
|
EYS
|
eyes shut homolog (Drosophila)
|
|
IFT140
|
intraflagellar transport 140
|
|
KIAA0586
|
KIAA0586
|
|
MVK
|
mevalonate kinase
|
|
NAGLU
|
N-acetylglucosaminidase, alpha
|
|
NIPAL1
|
NIPA-like domain containing 1
|
|
PCDH15
|
protocadherin-related 15
|
|
PHF3
|
PHD finger protein 3
|
|
PIGX
|
phosphatidylinositol glycan anchor biosynthesis, class X
|
|
PPT1
|
palmitoyl-protein thioesterase 1
|
|
RHO
|
rhodopsin
|
|
RPE65
|
retinal pigment epithelium-specific protein 65kDa
|
|
RPGRIP1
|
retinitis pigmentosa GTPase regulator interacting protein 1
|
|
SCAPER
|
S-phase cyclin A-associated protein in the ER
|
|
TBCK
|
TBC1 domain containing kinase
|
|
TUB
|
tubby bipartite transcription factor
|
|
USH1G
|
Usher syndrome 1G (autosomal recessive)
|
|
USH2A
|
Usher syndrome 2A (autosomal recessive, mild)
|
|
ZDHHC24
|
zinc finger, DHHC-type containing 24
|
