ectopic cerebellar granule cells Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description granule cell body resides in a place other than the external or internal granule layer of the cerebellum (Mammalian Phenotype Ontology, MP_0002762)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002762
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Genes

13 gene mutations causing the ectopic cerebellar granule cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABL1 ABL proto-oncogene 1, non-receptor tyrosine kinase
AKT3 v-akt murine thymoma viral oncogene homolog 3
APC2 adenomatosis polyposis coli 2
ASTN1 astrotactin 1
CDK5R1 cyclin-dependent kinase 5, regulatory subunit 1 (p35)
LYST lysosomal trafficking regulator
PLXNA2 plexin A2
PLXNB2 plexin B2
POMK protein-O-mannose kinase
POU1F1 POU class 1 homeobox 1
RORA RAR-related orphan receptor A
SEMA4C sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C
UNC5C unc-5 homolog C (C. elegans)