jerky movement Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description continuous, abrupt, faltering motions of the whole body or a portion of the body (Mammalian Phenotype Ontology, MP_0005424)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005424
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Genes

15 gene mutations causing the jerky movement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AFF1 AF4/FMR2 family, member 1
ASPA aspartoacylase
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase)
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
GRID2 glutamate receptor, ionotropic, delta 2
HPRT1 hypoxanthine phosphoribosyltransferase 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
MYO7A myosin VIIA
NOX3 NADPH oxidase 3
OCA2 oculocutaneous albinism II
PPT1 palmitoyl-protein thioesterase 1
PPT2 palmitoyl-protein thioesterase 2
SCN1A sodium channel, voltage gated, type I alpha subunit
TRAK1 trafficking protein, kinesin binding 1