clumsiness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lack of physical coordination resulting in an abnormal tendency to drop items or bump into objects. (Human Phenotype Ontology, HP_0002312)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002312
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Genes

12 genes associated with the clumsiness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C10ORF2 chromosome 10 open reading frame 2
CAPN3 calpain 3, (p94)
CDKL5 cyclin-dependent kinase-like 5
CLN5 ceroid-lipofuscinosis, neuronal 5
CLN8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
HEPACAM hepatic and glial cell adhesion molecule
MECP2 methyl CpG binding protein 2
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
SLC52A2 solute carrier family 52 (riboflavin transporter), member 2
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3
TPP1 tripeptidyl peptidase I
UBE3A ubiquitin protein ligase E3A