abnormal cortical ventricular zone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a transient region of the developing cerebral cortex that contains migrating neurons, radial glial cells, and a large population of cycling multipotent neural stem cells that generate newborn neurons (Mammalian Phenotype Ontology, MP_0008458)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008458
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Genes

11 gene mutations causing the abnormal cortical ventricular zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARX aristaless related homeobox
GNB1 guanine nucleotide binding protein (G protein), beta polypeptide 1
KIF20B kinesin family member 20B
NAPA N-ethylmaleimide-sensitive factor attachment protein, alpha
PAX6 paired box 6
PTBP2 polypyrimidine tract binding protein 2
SMARCA1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1
SOX11 SRY (sex determining region Y)-box 11
SPTAN1 spectrin, alpha, non-erythrocytic 1
TP53BP2 tumor protein p53 binding protein 2
ZBTB18 zinc finger and BTB domain containing 18