absent optic placodes Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the paired thickenings of surface ectoderm that normally become invaginated to form the embryonic lens vesicles (Mammalian Phenotype Ontology, MP_0012170)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012170
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3 gene mutations causing the absent optic placodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CSK c-src tyrosine kinase
LHX2 LIM homeobox 2
SMAD2 SMAD family member 2