abnormal cerebral cortex pyramidal cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the projection neurons in the pyramidal cell layer of the cerebral cortex (Mammalian Phenotype Ontology, MP_0009969)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009969
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Genes

25 gene mutations causing the abnormal cerebral cortex pyramidal cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABI2 abl-interactor 2
ABL2 ABL proto-oncogene 2, non-receptor tyrosine kinase
BRAF B-Raf proto-oncogene, serine/threonine kinase
CDK5R1 cyclin-dependent kinase 5, regulatory subunit 1 (p35)
CHL1 cell adhesion molecule L1-like
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
CLCN3 chloride channel, voltage-sensitive 3
CLCN7 chloride channel, voltage-sensitive 7
CNTN6 contactin 6
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
FGF2 fibroblast growth factor 2 (basic)
FOXG1 forkhead box G1
GM2A GM2 ganglioside activator
JAM3 junctional adhesion molecule 3
KALRN kalirin, RhoGEF kinase
KAT6B K(lysine) acetyltransferase 6B
KIF14 kinesin family member 14
MANBA mannosidase, beta A, lysosomal
MAPK8IP3 mitogen-activated protein kinase 8 interacting protein 3
OTC ornithine carbamoyltransferase
PCMT1 protein-L-isoaspartate (D-aspartate) O-methyltransferase
PTPRA protein tyrosine phosphatase, receptor type, A
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
TUBA1A tubulin, alpha 1a