severe myopia Gene Set
Genes
18 genes associated with the severe myopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ADAMTS10
|
ADAM metallopeptidase with thrombospondin type 1 motif, 10
|
|
ADAMTSL4
|
ADAMTS-like 4
|
|
CNGB3
|
cyclic nucleotide gated channel beta 3
|
|
COL18A1
|
collagen, type XVIII, alpha 1
|
|
COL9A1
|
collagen, type IX, alpha 1
|
|
COL9A2
|
collagen, type IX, alpha 2
|
|
ELOVL4
|
ELOVL fatty acid elongase 4
|
|
ERBB3
|
erb-b2 receptor tyrosine kinase 3
|
|
FBN1
|
fibrillin 1
|
|
IRX5
|
iroquois homeobox 5
|
|
LRP2
|
low density lipoprotein receptor-related protein 2
|
|
NYX
|
nyctalopin
|
|
P3H2
|
prolyl 3-hydroxylase 2
|
|
RAB28
|
RAB28, member RAS oncogene family
|
|
SLITRK6
|
SLIT and NTRK-like family, member 6
|
|
SMS
|
spermine synthase
|
|
TBC1D24
|
TBC1 domain family, member 24
|
|
ZNF644
|
zinc finger protein 644
|
