Aphakia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description absence of the crystalline lens of the eye (Mammalian Phenotype Ontology, MP_0003078)
External Link https://www.disgenet.org/browser/0/1/0/C1853230
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Genes

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

Symbol Name
ADK adenosine kinase
ALB albumin
CPA1 carboxypeptidase A1 (pancreatic)
CPA2 carboxypeptidase A2 (pancreatic)
CPB1 carboxypeptidase B1 (tissue)
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
CRYAB crystallin, alpha B
CYP4F3 cytochrome P450, family 4, subfamily F, polypeptide 3
FOXE3 forkhead box E3
GRM5 glutamate receptor, metabotropic 5
IFNG interferon, gamma
NTM neurotrimin
PAX6 paired box 6
PITX3 paired-like homeodomain 3
PTCH1 patched 1
SOD2 superoxide dismutase 2, mitochondrial
TP53 tumor protein p53