absent nasal capsule Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the cartilage around the developing nasal cavity of the embryo (Mammalian Phenotype Ontology, MP_0008384)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008384
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2 gene mutations causing the absent nasal capsule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
OTX2 orthodenticle homeobox 2
PCSK6 proprotein convertase subtilisin/kexin type 6