increased incidence of corneal inflammation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than average occurrence and/or persistence of the local accumulation of fluid, plasma proteins, and leukocytes in the cornea (Mammalian Phenotype Ontology, MP_0001313)
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14 gene mutations causing the increased incidence of corneal inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
AIRE autoimmune regulator
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CAMP cathelicidin antimicrobial peptide
CSTB cystatin B (stefin B)
EDA ectodysplasin A
FOXN1 forkhead box N1
INHBB inhibin, beta B
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LIMK2 LIM domain kinase 2
MYH9 myosin, heavy chain 9, non-muscle
NRTN neurturin
SOCS1 suppressor of cytokine signaling 1
TGFA transforming growth factor, alpha