apraxia Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description An agnosia that is a loss of the ability to map out physical actions in order to repeat them in functional activities. (Human Disease Ontology, DOID_0060135)
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Genes

8 genes co-occuring with the biological term apraxia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
APOE apolipoprotein E
APTX aprataxin
ARX aristaless related homeobox
MRE11A MRE11 meiotic recombination 11 homolog A (S. cerevisiae)
NPHP1 nephronophthisis 1 (juvenile)
POLG polymerase (DNA directed), gamma
SETX senataxin
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8