thin external granule cell layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced thickness of the transient layer of the cerebellar cortex present during development which is composed of dividing and migrating granule cells (Mammalian Phenotype Ontology, MP_0000873)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000873
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Genes

11 gene mutations causing the thin external granule cell layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACP2 acid phosphatase 2, lysosomal
CCND2 cyclin D2
CXCL12 chemokine (C-X-C motif) ligand 12
CXCR4 chemokine (C-X-C motif) receptor 4
EN2 engrailed homeobox 2
GLI2 GLI family zinc finger 2
GPR37L1 G protein-coupled receptor 37 like 1
GRID2 glutamate receptor, ionotropic, delta 2
INPP4A inositol polyphosphate-4-phosphatase, type I, 107kDa
LMNB2 lamin B2
RPL27A ribosomal protein L27a