Miosis Disorder Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0026205
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Genes

20 genes associated with the disease Miosis Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADCYAP1 adenylate cyclase activating polypeptide 1 (pituitary)
AP3D1 adaptor-related protein complex 3, delta 1 subunit
CHRDL1 chordin-like 1
COL4A2 collagen, type IV, alpha 2
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase)
DNMBP dynamin binding protein
FLT4 fms-related tyrosine kinase 4
HHAT hedgehog acyltransferase
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
OPN4 opsin 4
ORAI1 ORAI calcium release-activated calcium modulator 1
PANK2 pantothenate kinase 2
PEX7 peroxisomal biogenesis factor 7
PHYH phytanoyl-CoA 2-hydroxylase
PKD2L1 polycystic kidney disease 2-like 1
PLXNA2 plexin A2
POU2F1 POU class 2 homeobox 1
SIX6 SIX homeobox 6
SLC22A1 solute carrier family 22 (organic cation transporter), member 1
STIM1 stromal interaction molecule 1