broad-based gait Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal gait pattern in which persons stand and walk with their feet spaced widely apart. This is often a component of cerebellar ataxia. (Human Phenotype Ontology, HP_0002136)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002136
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Genes

19 genes associated with the broad-based gait phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADGRG1 adhesion G protein-coupled receptor G1
ATCAY ataxia, cerebellar, Cayman type
CDKL5 cyclin-dependent kinase-like 5
FLVCR1 feline leukemia virus subgroup C cellular receptor 1
HSD17B10 hydroxysteroid (17-beta) dehydrogenase 10
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
KMT2A lysine (K)-specific methyltransferase 2A
MECP2 methyl CpG binding protein 2
MYOT myotilin
NRXN1 neurexin 1
PIGL phosphatidylinositol glycan anchor biosynthesis, class L
SATB2 SATB homeobox 2
SHANK3 SH3 and multiple ankyrin repeat domains 3
SMS spermine synthase
TBP TATA box binding protein
TRIM2 tripartite motif containing 2
TRPV4 transient receptor potential cation channel, subfamily V, member 4
UBE3A ubiquitin protein ligase E3A
VLDLR very low density lipoprotein receptor