axonal degeneration/regeneration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A pattern of simultaneous degeneration and regeneration of axons (see comment). (Human Phenotype Ontology, HP_0003378)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003378
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Genes

7 genes associated with the axonal degeneration/regeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GDAP1 ganglioside induced differentiation associated protein 1
KIF1B kinesin family member 1B
LMNA lamin A/C
MFN2 mitofusin 2
MPZ myelin protein zero
RAB7A RAB7A, member RAS oncogene family
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6