abnormal stratification in cerebral cortex Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal formation or pattern of the layers of the cerebral cortex (Mammalian Phenotype Ontology, MP_0000790)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000790
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Genes

26 gene mutations causing the abnormal stratification in cerebral cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC2 adenomatosis polyposis coli 2
ARHGAP35 Rho GTPase activating protein 35
BRAF B-Raf proto-oncogene, serine/threonine kinase
CDK5 cyclin-dependent kinase 5
CDK5R1 cyclin-dependent kinase 5, regulatory subunit 1 (p35)
CLCN7 chloride channel, voltage-sensitive 7
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
FGF2 fibroblast growth factor 2 (basic)
FKRP fukutin related protein
FOXC1 forkhead box C1
FYN FYN proto-oncogene, Src family tyrosine kinase
GLI3 GLI family zinc finger 3
HSPA5 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)
ID4 inhibitor of DNA binding 4, dominant negative helix-loop-helix protein
KIF2A kinesin heavy chain member 2A
LMNB1 lamin B1
LMNB2 lamin B2
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PEX2 peroxisomal biogenesis factor 2
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
PSEN1 presenilin 1
RELN reelin
SUZ12 SUZ12 polycomb repressive complex 2 subunit
TOP2B topoisomerase (DNA) II beta 180kDa
TP53BP2 tumor protein p53 binding protein 2
TTL tubulin tyrosine ligase