abnormal olfactory bulb layer morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the laminar structure of the forebrain region that coordinates neuronal signaling involved in the perception of smell (Mammalian Phenotype Ontology, MP_0009946)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009946
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19 gene mutations causing the abnormal olfactory bulb layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTPBP1 ATP/GTP binding protein 1
APC2 adenomatosis polyposis coli 2
CCDC88A coiled-coil domain containing 88A
CNGA3 cyclic nucleotide gated channel alpha 3
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
DLX5 distal-less homeobox 5
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
IGF1 insulin-like growth factor 1 (somatomedin C)
KIRREL3 kin of IRRE like 3 (Drosophila)
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
NMNAT2 nicotinamide nucleotide adenylyltransferase 2
PINK1 PTEN induced putative kinase 1
RELN reelin
RORA RAR-related orphan receptor A
SH2D3C SH2 domain containing 3C
TBR1 T-box, brain, 1
TSHZ1 teashirt zinc finger homeobox 1
ZEB1 zinc finger E-box binding homeobox 1