abnormal postnatal subventricular zone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the mitotically active layer of cells surrounding the brain ventricles in the adult that consists of migrating neuroblasts, astrocytes and transitory amplifying progenitor cells (Mammalian Phenotype Ontology, MP_0004275)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004275
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Genes

22 gene mutations causing the abnormal postnatal subventricular zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARX aristaless related homeobox
CCDC88A coiled-coil domain containing 88A
CCKAR cholecystokinin A receptor
CLN3 ceroid-lipofuscinosis, neuronal 3
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
DLG5 discs, large homolog 5 (Drosophila)
FOXJ1 forkhead box J1
FZR1 fizzy/cell division cycle 20 related 1 (Drosophila)
HTT huntingtin
LGALS1 lectin, galactoside-binding, soluble, 1
LRP8 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor
MCM2 minichromosome maintenance complex component 2
NCAM1 neural cell adhesion molecule 1
NPY1R neuropeptide Y receptor Y1
NPY2R neuropeptide Y receptor Y2
PAX6 paired box 6
RAB23 RAB23, member RAS oncogene family
RBL1 retinoblastoma-like 1
RELN reelin
SHH sonic hedgehog
VAX1 ventral anterior homeobox 1
ZBTB18 zinc finger and BTB domain containing 18