abnormal central pattern generator function Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the neural networks that produce rhythmic patterned output without sensory input and underlie rhythmic motor patterns (Mammalian Phenotype Ontology, MP_0003880)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003880
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11 gene mutations causing the abnormal central pattern generator function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHN1 chimerin 1
DBX1 developing brain homeobox 1
DSCAM Down syndrome cell adhesion molecule
EFNB3 ephrin-B3
EPHA4 EPH receptor A4
KDM6B lysine (K)-specific demethylase 6B
NDN necdin, melanoma antigen (MAGE) family member
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
ROBO3 roundabout, axon guidance receptor, homolog 3 (Drosophila)
SLC12A5 solute carrier family 12 (potassium/chloride transporter), member 5
SLC17A6 solute carrier family 17 (vesicular glutamate transporter), member 6