cone-rod dystrophy Gene Set
Genes
22 genes involed in the disease cone-rod dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
| Symbol |
Name |
|
ABCA4
|
ATP-binding cassette, sub-family A (ABC1), member 4
|
|
ADAM9
|
ADAM metallopeptidase domain 9
|
|
ALMS1
|
Alstrom syndrome protein 1
|
|
C8ORF37
|
chromosome 8 open reading frame 37
|
|
CACNA1F
|
calcium channel, voltage-dependent, L type, alpha 1F subunit
|
|
CDHR1
|
cadherin-related family member 1
|
|
CNNM4
|
cyclin and CBS domain divalent metal cation transport mediator 4
|
|
CRX
|
cone-rod homeobox
|
|
GUCY2D
|
guanylate cyclase 2D, membrane (retina-specific)
|
|
KCNV2
|
potassium channel, voltage gated modifier subfamily V, member 2
|
|
PCYT1A
|
phosphate cytidylyltransferase 1, choline, alpha
|
|
PITPNM3
|
PITPNM family member 3
|
|
PROM1
|
prominin 1
|
|
PRPH2
|
peripherin 2 (retinal degeneration, slow)
|
|
RAB28
|
RAB28, member RAS oncogene family
|
|
RAX2
|
retina and anterior neural fold homeobox 2
|
|
RIMS1
|
regulating synaptic membrane exocytosis 1
|
|
RPGR
|
retinitis pigmentosa GTPase regulator
|
|
RPGRIP1
|
retinitis pigmentosa GTPase regulator interacting protein 1
|
|
SEMA4A
|
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
|
|
TTLL5
|
tubulin tyrosine ligase-like family member 5
|
|
UNC119
|
unc-119 homolog (C. elegans)
|
