poor head control Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Difficulty to maintain correct position of the head while standing or sitting. (Human Phenotype Ontology, HP_0002421)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002421
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Genes

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

Symbol Name
DHFR dihydrofolate reductase
EXOSC3 exosome component 3
FKBP14 FK506 binding protein 14, 22 kDa
GM2A GM2 ganglioside activator
GMPPB GDP-mannose pyrophosphorylase B
HEXA hexosaminidase A (alpha polypeptide)
MEGF10 multiple EGF-like-domains 10
POMK protein-O-mannose kinase
RARS2 arginyl-tRNA synthetase 2, mitochondrial
SEPN1 selenoprotein N, 1
SNAP29 synaptosomal-associated protein, 29kDa
TREX1 three prime repair exonuclease 1