scotoma Gene Set
Genes
15 genes associated with the scotoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ABCA4
|
ATP-binding cassette, sub-family A (ABC1), member 4
|
|
C12ORF65
|
chromosome 12 open reading frame 65
|
|
C1QTNF5
|
C1q and tumor necrosis factor related protein 5
|
|
CACNA1F
|
calcium channel, voltage-dependent, L type, alpha 1F subunit
|
|
COL4A1
|
collagen, type IV, alpha 1
|
|
FLVCR1
|
feline leukemia virus subgroup C cellular receptor 1
|
|
KCNV2
|
potassium channel, voltage gated modifier subfamily V, member 2
|
|
MFN2
|
mitofusin 2
|
|
OPA1
|
optic atrophy 1 (autosomal dominant)
|
|
PROM1
|
prominin 1
|
|
PRPF3
|
pre-mRNA processing factor 3
|
|
RAB28
|
RAB28, member RAS oncogene family
|
|
RBP3
|
retinol binding protein 3, interstitial
|
|
RLBP1
|
retinaldehyde binding protein 1
|
|
TMEM126A
|
transmembrane protein 126A
|
