abnormal optic placode morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the paired thickenings of surface ectoderm that become invaginated to form the embryonic lens vesicles (Mammalian Phenotype Ontology, MP_0012168)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012168
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6 gene mutations causing the abnormal optic placode morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CSK c-src tyrosine kinase
LHX2 LIM homeobox 2
MAB21L1 mab-21-like 1 (C. elegans)
PAX6 paired box 6
SMAD2 SMAD family member 2
ZNRF3 zinc and ring finger 3