abnormal optic pit morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the depression found on each side of the end of the neural ectoderm (or neural tube) of the embryo; the pit deepens to form the optic vesicle (Mammalian Phenotype Ontology, MP_0012155)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012155
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Genes

4 gene mutations causing the abnormal optic pit morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
OVOL2 ovo-like zinc finger 2
RAX retina and anterior neural fold homeobox
SIX3 SIX homeobox 3
SMG1 SMG1 phosphatidylinositol 3-kinase-related kinase