muscle hypertonia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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9 gene mutations causing the muscle hypertonia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASPA aspartoacylase
CLCN1 chloride channel, voltage-sensitive 1
DSCAM Down syndrome cell adhesion molecule
GLRA1 glycine receptor, alpha 1
GLRB glycine receptor, beta
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SLC32A1 solute carrier family 32 (GABA vesicular transporter), member 1
SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 5
WNT1 wingless-type MMTV integration site family, member 1