Regular Astigmatism - Corneal Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0339682
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Genes

32 genes associated with the disease Regular Astigmatism - Corneal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACP2 acid phosphatase 2, lysosomal
ADAMTS8 ADAM metallopeptidase with thrombospondin type 1 motif, 8
ART1 ADP-ribosyltransferase 1
ATR ATR serine/threonine kinase
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
C1QL1 complement component 1, q subcomponent-like 1
CCL1 chemokine (C-C motif) ligand 1
CLDN7 claudin 7
CRH corticotropin releasing hormone
DNAH5 dynein, axonemal, heavy chain 5
DOCK9 dedicator of cytokinesis 9
ETV5 ets variant 5
FLI1 Fli-1 proto-oncogene, ETS transcription factor
FMNL2 formin-like 2
HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2
LRRC23 leucine rich repeat containing 23
MATN3 matrilin 3
MED13L mediator complex subunit 13-like
NPLOC4 nuclear protein localization 4 homolog (S. cerevisiae)
OCA2 oculocutaneous albinism II
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
PITX2 paired-like homeodomain 2
SLC25A1 solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1
SMAD3 SMAD family member 3
SPSB2 splA/ryanodine receptor domain and SOCS box containing 2
TIPE3 TNF alpha induced protein 8 like 3
TSPAN10 tetraspanin 10
TWIST1 twist family bHLH transcription factor 1
VAV2 vav 2 guanine nucleotide exchange factor
VAX2 ventral anterior homeobox 2
ZC3H11B zinc finger CCCH-type containing 11B pseudogene
ZNF469 zinc finger protein 469