abnormal eye muscle development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description malformation or arrest of differentiation of the muscles of the eye (Mammalian Phenotype Ontology, MP_0003818)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003818
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2 gene mutations causing the abnormal eye muscle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MYF5 myogenic factor 5
PITX2 paired-like homeodomain 2