segmental peripheral demyelination/remyelination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A segmental pattern of demyelination and regeneration (remyelination) affecting peripheral nerves. (Human Phenotype Ontology, HP_0003481)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003481
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Genes

10 genes associated with the segmental peripheral demyelination/remyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DNM2 dynamin 2
EGR2 early growth response 2
LITAF lipopolysaccharide-induced TNF factor
MPZ myelin protein zero
NDRG1 N-myc downstream regulated 1
NEFL neurofilament, light polypeptide
PMP22 peripheral myelin protein 22
PRPS1 phosphoribosyl pyrophosphate synthetase 1
PRX periaxin
SBF2 SET binding factor 2