abnormal cortical marginal zone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the developing superficial cortical layer located just under the pia matter (Mammalian Phenotype Ontology, MP_0000792)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000792
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16 gene mutations causing the abnormal cortical marginal zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRG1 adhesion G protein-coupled receptor G1
APAF1 apoptotic peptidase activating factor 1
ARX aristaless related homeobox
CELSR3 cadherin, EGF LAG seven-pass G-type receptor 3
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
FOXC1 forkhead box C1
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
LAMC1 laminin, gamma 1 (formerly LAMB2)
MAPK8IP3 mitogen-activated protein kinase 8 interacting protein 3
MARCKS myristoylated alanine-rich protein kinase C substrate
NAPA N-ethylmaleimide-sensitive factor attachment protein, alpha
NEUROG2 neurogenin 2
PRX periaxin
PSEN1 presenilin 1
RELN reelin
TP73 tumor protein p73