no spontaneous movement Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure of neonates or embryos to initiate any voluntary or spontaneous change in position or posture, with or without external stimulus (Mammalian Phenotype Ontology, MP_0001404)
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23 gene mutations causing the no spontaneous movement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGRN agrin
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
DHCR7 7-dehydrocholesterol reductase
DLL1 delta-like 1 (Drosophila)
ERBB3 erb-b2 receptor tyrosine kinase 3
FBXO45 F-box protein 45
FGFRL1 fibroblast growth factor receptor-like 1
FOXG1 forkhead box G1
GNAS GNAS complex locus
ILF3 interleukin enhancer binding factor 3, 90kDa
LRP4 low density lipoprotein receptor-related protein 4
MUSK muscle, skeletal, receptor tyrosine kinase
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
MYOG myogenin (myogenic factor 4)
NBEA neurobeachin
NRG1 neuregulin 1
OLIG2 oligodendrocyte lineage transcription factor 2
RYR1 ryanodine receptor 1 (skeletal)
SLC32A1 solute carrier family 32 (GABA vesicular transporter), member 1
SNAP25 synaptosomal-associated protein, 25kDa
TSHZ3 teashirt zinc finger homeobox 3