severe myopia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A severe form of myopia with greater than -6.00 diopters. (Human Phenotype Ontology, HP_0011003)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011003
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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