impaired muscle relaxation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003157
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Genes

15 gene mutations causing the impaired muscle relaxation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
AR androgen receptor
ATP2A1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1
CASQ1 calsequestrin 1 (fast-twitch, skeletal muscle)
CLCN1 chloride channel, voltage-sensitive 1
COL19A1 collagen, type XIX, alpha 1
DMD dystrophin
MBNL2 muscleblind-like splicing regulator 2
MRVI1 murine retrovirus integration site 1 homolog
MYBPC3 myosin binding protein C, cardiac
NPR2 natriuretic peptide receptor 2
PRKG1 protein kinase, cGMP-dependent, type I
RYR1 ryanodine receptor 1 (skeletal)
SCN4A sodium channel, voltage gated, type IV alpha subunit
TARDBP TAR DNA binding protein