anosmia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An inability to perceive odors. This is a general term describing inability to smell arising in any part of the process of smelling from absorption of odorants into the nasal mucous overlying the olfactory epithelium, diffusion to the cilia, binding to olfactory receptor sites, generation of action potentials in olfactory neurons, and perception of a smell. (Human Phenotype Ontology, HP_0000458)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004512
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Genes

5 gene mutations causing the anosmia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY3 adenylate cyclase 3
CEP290 centrosomal protein 290kDa
CNGA2 cyclic nucleotide gated channel alpha 2
MKKS McKusick-Kaufman syndrome
UBR3 ubiquitin protein ligase E3 component n-recognin 3 (putative)