peripheral hypomyelination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced amount of myelin in the nervous system resulting from defective myelinogenesis in the peripheral nervous system. (Human Phenotype Ontology, HP_0007182)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007182
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Genes

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

Symbol Name
CTDP1 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
EGR2 early growth response 2
FIG4 FIG4 phosphoinositide 5-phosphatase
GDAP1 ganglioside induced differentiation associated protein 1
HK1 hexokinase 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
MPZ myelin protein zero
SOX10 SRY (sex determining region Y)-box 10