abnormal purkinje cell dendrite morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the Purkinje cell body projections with hundreds of parallel spiny branches reaching up into the molecular layer (Mammalian Phenotype Ontology, MP_0008572)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008572
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36 gene mutations causing the abnormal purkinje cell dendrite morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACP2 acid phosphatase 2, lysosomal
AGTPBP1 ATP/GTP binding protein 1
ARCN1 archain 1
ATM ATM serine/threonine kinase
ATXN1 ataxin 1
BCL2L2 BCL2-like 2
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CADPS2 Ca++-dependent secretion activator 2
CAMK4 calcium/calmodulin-dependent protein kinase IV
CCND2 cyclin D2
CEND1 cell cycle exit and neuronal differentiation 1
CERS1 ceramide synthase 1
DAB2IP DAB2 interacting protein
DNM1 dynamin 1
DPYSL5 dihydropyrimidinase-like 5
FOXP2 forkhead box P2
GAS1 growth arrest-specific 1
GRID2 glutamate receptor, ionotropic, delta 2
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6
KIF14 kinesin family member 14
MAP1B microtubule-associated protein 1B
MAPK8IP2 mitogen-activated protein kinase 8 interacting protein 2
MYH10 myosin, heavy chain 10, non-muscle
MYO5A myosin VA (heavy chain 12, myoxin)
NR1D1 nuclear receptor subfamily 1, group D, member 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PREX2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2
RORA RAR-related orphan receptor A
SCYL1 SCY1-like 1 (S. cerevisiae)
SPTBN2 spectrin, beta, non-erythrocytic 2
STK38L serine/threonine kinase 38 like
STUB1 STIP1 homology and U-box containing protein 1, E3 ubiquitin protein ligase
TOR1A torsin family 1, member A (torsin A)
TRPC3 transient receptor potential cation channel, subfamily C, member 3
VIM vimentin
ZNF423 zinc finger protein 423