absent olfactory bulb Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the forebrain region that coordinates neuronal signaling involved in the perception of smell; it receives input from the sensory neurons and outputs to the olfactory cortex (Mammalian Phenotype Ontology, MP_0003451)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003451
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Genes

12 gene mutations causing the absent olfactory bulb phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
CSK c-src tyrosine kinase
FGF8 fibroblast growth factor 8 (androgen-induced)
GLI3 GLI family zinc finger 3
LRP2 low density lipoprotein receptor-related protein 2
NCOA6 nuclear receptor coactivator 6
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
OTX2 orthodenticle homeobox 2
PAX6 paired box 6
PHGDH phosphoglycerate dehydrogenase
RPGRIP1L RPGRIP1-like
TTC21B tetratricopeptide repeat domain 21B