abnormal olfactory system physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the system relating to smell (Mammalian Phenotype Ontology, MP_0001983)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001983
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Genes

46 gene mutations causing the abnormal olfactory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY3 adenylate cyclase 3
ADH7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide
ADRBK2 adrenergic, beta, receptor kinase 2
ANO2 anoctamin 2, calcium activated chloride channel
APOE apolipoprotein E
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
ATP6V1B1 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
B3GNT2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2
BBS1 Bardet-Biedl syndrome 1
BBS2 Bardet-Biedl syndrome 2
BBS4 Bardet-Biedl syndrome 4
CEP290 centrosomal protein 290kDa
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
CNGA2 cyclic nucleotide gated channel alpha 2
CNGA3 cyclic nucleotide gated channel alpha 3
CNGA4 cyclic nucleotide gated channel alpha 4
CNTNAP2 contactin associated protein-like 2
FYN FYN proto-oncogene, Src family tyrosine kinase
FZD2 frizzled class receptor 2
GABRR1 gamma-aminobutyric acid (GABA) A receptor, rho 1
GFY golgi-associated, olfactory signaling regulator
GJB4 gap junction protein, beta 4, 30.3kDa
GNAL guanine nucleotide binding protein (G protein), alpha activating activity polypeptide, olfactory type
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
HIST1H2BJ histone cluster 1, H2bj
ID2 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
MAGEL2 melanoma antigen family L2
MKKS McKusick-Kaufman syndrome
NAV2 neuron navigator 2
NCAM2 neural cell adhesion molecule 2
NLGN3 neuroligin 3
NPC1 Niemann-Pick disease, type C1
NXNL2 nucleoredoxin-like 2
OMP olfactory marker protein
OR8A1 olfactory receptor, family 8, subfamily A, member 1
PDE1C phosphodiesterase 1C, calmodulin-dependent 70kDa
PEBP1 phosphatidylethanolamine binding protein 1
PINK1 PTEN induced putative kinase 1
PTPRS protein tyrosine phosphatase, receptor type, S
RORA RAR-related orphan receptor A
SLC18A2 solute carrier family 18 (vesicular monoamine transporter), member 2
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4
TAAR5 trace amine associated receptor 5
TERT telomerase reverse transcriptase
TTC8 tetratricopeptide repeat domain 8
UBR3 ubiquitin protein ligase E3 component n-recognin 3 (putative)