chorioretinal atrophy Gene Set
Genes
11 genes associated with the chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
CRB1
|
crumbs family member 1, photoreceptor morphogenesis associated
|
|
CRX
|
cone-rod homeobox
|
|
FSCN2
|
fascin actin-bundling protein 2, retinal
|
|
JAG1
|
jagged 1
|
|
NRL
|
neural retina leucine zipper
|
|
OAT
|
ornithine aminotransferase
|
|
PAX2
|
paired box 2
|
|
SAG
|
S-antigen; retina and pineal gland (arrestin)
|
|
SLC25A15
|
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
|
|
TEAD1
|
TEA domain family member 1 (SV40 transcriptional enhancer factor)
|
|
VCAN
|
versican
|
