abnormal radial glial cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the supporting cells of the developing central nervous system that guide neuronal migration during development and exchange metabolites with developing and migrating neurons; these cells differentiate into astrocytes and some neuronal types in the adult (Mammalian Phenotype Ontology, MP_0003648)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003648
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15 gene mutations causing the abnormal radial glial cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRG1 adhesion G protein-coupled receptor G1
FKRP fukutin related protein
FOXC1 forkhead box C1
FOXP2 forkhead box P2
GLI3 GLI family zinc finger 3
HSPG2 heparan sulfate proteoglycan 2
ISPD isoprenoid synthase domain containing
ITGB8 integrin, beta 8
LAMC1 laminin, gamma 1 (formerly LAMB2)
NEUROG2 neurogenin 2
NR2E1 nuclear receptor subfamily 2, group E, member 1
NRG1 neuregulin 1
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PLXNB2 plexin B2
RORA RAR-related orphan receptor A