abnormal olfactory epithelium morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the epithelial cells that line the interior of the nose (Mammalian Phenotype Ontology, MP_0008789)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008789
Similar Terms
Downloads & Tools

Genes

42 gene mutations causing the abnormal olfactory epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AQP3 aquaporin 3 (Gill blood group)
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
CASP3 caspase 3, apoptosis-related cysteine peptidase
CASP9 caspase 9, apoptosis-related cysteine peptidase
CCKAR cholecystokinin A receptor
CEP290 centrosomal protein 290kDa
CHL1 cell adhesion molecule L1-like
CNGA2 cyclic nucleotide gated channel alpha 2
DLX5 distal-less homeobox 5
E2F4 E2F transcription factor 4, p107/p130-binding
EBF2 early B-cell factor 2
FEZF1 FEZ family zinc finger 1
FOXG1 forkhead box G1
FST follistatin
GDF11 growth differentiation factor 11
GFY golgi-associated, olfactory signaling regulator
GLI3 GLI family zinc finger 3
GSC goosecoid homeobox
GSX2 GS homeobox 2
HESX1 HESX homeobox 1
HIST1H2BJ histone cluster 1, H2bj
INSM1 insulinoma-associated 1
ITGB4 integrin, beta 4
LGALS1 lectin, galactoside-binding, soluble, 1
MARVELD2 MARVEL domain containing 2
MKKS McKusick-Kaufman syndrome
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
OTX2 orthodenticle homeobox 2
PAX6 paired box 6
SIX1 SIX homeobox 1
TP63 tumor protein p63
TTC8 tetratricopeptide repeat domain 8
ZEB1 zinc finger E-box binding homeobox 1
ZNF423 zinc finger protein 423