tongue fasciculations Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Fasciculations or fibrillation affecting the tongue muscle. (Human Phenotype Ontology, HP_0001308)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001308
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Genes

10 genes associated with the tongue fasciculations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASAH1 N-acylsphingosine amidohydrolase (acid ceramidase) 1
NOP56 NOP56 ribonucleoprotein
OPTN optineurin
RMND1 required for meiotic nuclear division 1 homolog (S. cerevisiae)
SH3TC2 SH3 domain and tetratricopeptide repeats 2
SLC52A2 solute carrier family 52 (riboflavin transporter), member 2
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3
SMN1 survival of motor neuron 1, telomeric
TSPYL1 TSPY-like 1
UBA1 ubiquitin-like modifier activating enzyme 1