thin cerebellar granule layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced thickness of the innermost cortical layer of the cerebellum that contains granule cells (Mammalian Phenotype Ontology, MP_0006099)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006099
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Genes

9 gene mutations causing the thin cerebellar granule layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASTN1 astrotactin 1
CIT citron rho-interacting serine/threonine kinase
GAS1 growth arrest-specific 1
GRIN2C glutamate receptor, ionotropic, N-methyl D-aspartate 2C
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6
NEUROD4 neuronal differentiation 4
RB1 retinoblastoma 1
RORA RAR-related orphan receptor A
TP53 tumor protein p53