abnormal cerebellar granule cell migration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the movement of cerebellar granule cell neurons from the germinal zone into the granule cell layer of the cerebellum along radial glia fibers during development of the cerebellar cortex (Mammalian Phenotype Ontology, MP_0009977)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009977
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10 gene mutations causing the abnormal cerebellar granule cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC2 adenomatosis polyposis coli 2
ASS1 argininosuccinate synthase 1
ASTN1 astrotactin 1
CADPS2 Ca++-dependent secretion activator 2
CEND1 cell cycle exit and neuronal differentiation 1
GNPAT glyceronephosphate O-acyltransferase
KIF14 kinesin family member 14
PLXNB2 plexin B2
POMK protein-O-mannose kinase
SEMA4C sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C