olfactory bulb hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, of the forebrain region that coordinates neuronal signaling involved in the perception of smell (Mammalian Phenotype Ontology, MP_0010059)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010059
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2 gene mutations causing the olfactory bulb hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SH2D3C SH2 domain containing 3C
TBR1 T-box, brain, 1