absent sclera Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the fibrous, outer envelope of the eyeball, covering it entirely excepting the segment covered anteriorly by the cornea (Mammalian Phenotype Ontology, MP_0010710)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010710
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1 gene mutations causing the absent sclera phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
RXRA retinoid X receptor, alpha