abnormal motor learning Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the ability to repeat a motor task requiring well coordinated movements and balance; measures cerebellar dependent learning (Mammalian Phenotype Ontology, MP_0002804)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002804
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Genes

36 gene mutations causing the abnormal motor learning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
APOD apolipoprotein D
ARL6IP5 ADP-ribosylation factor-like 6 interacting protein 5
ATG4B autophagy related 4B, cysteine peptidase
ATM ATM serine/threonine kinase
BCL2L2 BCL2-like 2
CERS1 ceramide synthase 1
CHRNA4 cholinergic receptor, nicotinic, alpha 4 (neuronal)
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase)
DOCK3 dedicator of cytokinesis 3
FA2H fatty acid 2-hydroxylase
FOXP2 forkhead box P2
GJC2 gap junction protein, gamma 2, 47kDa
GPR37L1 G protein-coupled receptor 37 like 1
GRID2 glutamate receptor, ionotropic, delta 2
GRM4 glutamate receptor, metabotropic 4
HCN1 hyperpolarization activated cyclic nucleotide gated potassium channel 1
MAPT microtubule-associated protein tau
MECP2 methyl CpG binding protein 2
MID1 midline 1
NQO2 NAD(P)H dehydrogenase, quinone 2
NRCAM neuronal cell adhesion molecule
NRXN1 neurexin 1
PARK7 parkinson protein 7
PCP4 Purkinje cell protein 4
PEX5L peroxisomal biogenesis factor 5-like
PLAT plasminogen activator, tissue
RAC3 ras-related C3 botulinum toxin substrate 3 (rho family, small GTP binding protein Rac3)
RORA RAR-related orphan receptor A
SHANK3 SH3 and multiple ankyrin repeat domains 3
SLC24A2 solute carrier family 24 (sodium/potassium/calcium exchanger), member 2
SST somatostatin
UBE3A ubiquitin protein ligase E3A
UNC13C unc-13 homolog C (C. elegans)
VIM vimentin
ZDHHC13 zinc finger, DHHC-type containing 13