blepharitis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An eyelid disease that is characterized by often chronic inflammation of the eyelid, generally the part where eyelashes grow. (Human Disease Ontology, DOID_9423)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005251
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Genes

14 gene mutations causing the blepharitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EDA ectodysplasin A
FOXN1 forkhead box N1
FOXP3 forkhead box P3
KMT2E lysine (K)-specific methyltransferase 2E
NFKBIZ nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, zeta
ORAI1 ORAI calcium release-activated calcium modulator 1
PPIA peptidylprolyl isomerase A (cyclophilin A)
PSIP1 PC4 and SFRS1 interacting protein 1
RAD23B RAD23 homolog B (S. cerevisiae)
ROCK1 Rho-associated, coiled-coil containing protein kinase 1
SH3BP2 SH3-domain binding protein 2
SNAI2 snail family zinc finger 2
TMEM79 transmembrane protein 79
TRAF3IP2 TRAF3 interacting protein 2