abnormal olfactory bulb development Gene Set
Genes
28 gene mutations causing the abnormal olfactory bulb development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Symbol |
Name |
CASP3
|
caspase 3, apoptosis-related cysteine peptidase
|
CCDC88A
|
coiled-coil domain containing 88A
|
CCKAR
|
cholecystokinin A receptor
|
CDK5
|
cyclin-dependent kinase 5
|
CDK5R1
|
cyclin-dependent kinase 5, regulatory subunit 1 (p35)
|
DAB1
|
Dab, reelin signal transducer, homolog 1 (Drosophila)
|
DCX
|
doublecortin
|
DLX2
|
distal-less homeobox 2
|
DLX5
|
distal-less homeobox 5
|
FEZF1
|
FEZ family zinc finger 1
|
FOXJ1
|
forkhead box J1
|
ID2
|
inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
|
LRP8
|
low density lipoprotein receptor-related protein 8, apolipoprotein e receptor
|
NPY1R
|
neuropeptide Y receptor Y1
|
NPY2R
|
neuropeptide Y receptor Y2
|
OLIG3
|
oligodendrocyte transcription factor 3
|
OR10A4
|
olfactory receptor, family 10, subfamily A, member 4
|
OR51E2
|
olfactory receptor, family 51, subfamily E, member 2
|
OR8A1
|
olfactory receptor, family 8, subfamily A, member 1
|
PLXNB2
|
plexin B2
|
PROK2
|
prokineticin 2
|
PROKR2
|
prokineticin receptor 2
|
RELN
|
reelin
|
RTP1
|
receptor (chemosensory) transporter protein 1
|
TBR1
|
T-box, brain, 1
|
TDO2
|
tryptophan 2,3-dioxygenase
|
TFAP2E
|
transcription factor AP-2 epsilon (activating enhancer binding protein 2 epsilon)
|
VAX1
|
ventral anterior homeobox 1
|