mutism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A speech disorder that involves a complete inability to speak. (Human Disease Ontology, DOID_4189)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002300
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Genes

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

Symbol Name
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
CHMP2B charged multivesicular body protein 2B
CSF1R colony stimulating factor 1 receptor
FTL ferritin, light polypeptide
GRN granulin
MAPT microtubule-associated protein tau
SLC19A3 solute carrier family 19 (thiamine transporter), member 3
SLC9A6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
TBP TATA box binding protein