abnormal olfactory sensory neuron morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the neurons in the olfactory epithelium that are activated by specific odorants (Mammalian Phenotype Ontology, MP_0006092)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006092
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Genes

21 gene mutations causing the abnormal olfactory sensory neuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASCL1 achaete-scute family bHLH transcription factor 1
ATF5 activating transcription factor 5
B3GNT2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2
BBS1 Bardet-Biedl syndrome 1
BBS4 Bardet-Biedl syndrome 4
CCKAR cholecystokinin A receptor
CHL1 cell adhesion molecule L1-like
CNGA2 cyclic nucleotide gated channel alpha 2
EBF2 early B-cell factor 2
FEZF1 FEZ family zinc finger 1
FST follistatin
GDF11 growth differentiation factor 11
GSX2 GS homeobox 2
HIST1H2BJ histone cluster 1, H2bj
LGALS1 lectin, galactoside-binding, soluble, 1
NPC1 Niemann-Pick disease, type C1
NPY1R neuropeptide Y receptor Y1
NPY2R neuropeptide Y receptor Y2
NXNL2 nucleoredoxin-like 2
OR8A1 olfactory receptor, family 8, subfamily A, member 1
ZEB1 zinc finger E-box binding homeobox 1