absent ethmoidal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing midline facial bone that encloses the nasal cavity (Mammalian Phenotype Ontology, MP_0000101)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000101
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2 gene mutations causing the absent ethmoidal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
CTGF connective tissue growth factor