sensory axonal neuropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An axonal neuropathy of peripheral sensory nerves. (Human Phenotype Ontology, HP_0003390)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003390
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Genes

8 genes associated with the sensory axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATL3 atlastin GTPase 3
C10ORF2 chromosome 10 open reading frame 2
FGF14 fibroblast growth factor 14
GAN gigaxonin
GJC2 gap junction protein, gamma 2, 47kDa
HINT1 histidine triad nucleotide binding protein 1
POLG polymerase (DNA directed), gamma
PRICKLE1 prickle homolog 1 (Drosophila)