abnormal olfactory bulb development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormality in the progression of the formation of the olfactory bulb (Mammalian Phenotype Ontology, MP_0002739)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002739
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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