impaired olfaction Gene Set
Genes
18 gene mutations causing the impaired olfaction 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
|
|
APOE
|
apolipoprotein E
|
|
ATP6V0A4
|
ATPase, H+ transporting, lysosomal V0 subunit a4
|
|
BBS1
|
Bardet-Biedl syndrome 1
|
|
CHRNA7
|
cholinergic receptor, nicotinic, alpha 7 (neuronal)
|
|
GFY
|
golgi-associated, olfactory signaling regulator
|
|
GJB4
|
gap junction protein, beta 4, 30.3kDa
|
|
HIST1H2BJ
|
histone cluster 1, H2bj
|
|
MAGEL2
|
melanoma antigen family L2
|
|
NLGN3
|
neuroligin 3
|
|
NPC1
|
Niemann-Pick disease, type C1
|
|
NXNL2
|
nucleoredoxin-like 2
|
|
PTPRS
|
protein tyrosine phosphatase, receptor type, S
|
|
SLC18A2
|
solute carrier family 18 (vesicular monoamine transporter), member 2
|
|
SLC24A4
|
solute carrier family 24 (sodium/potassium/calcium exchanger), member 4
|
|
TERT
|
telomerase reverse transcriptase
|
|
TTC8
|
tetratricopeptide repeat domain 8
|
