peripheral nervous system degeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a retrogressive impairment of function or destruction of the ganglia and peripheral nerves that lie outside the brain and spinal cord (Mammalian Phenotype Ontology, MP_0000958)
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9 gene mutations causing the peripheral nervous system degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARSB arylsulfatase B
DST dystonin
GALC galactosylceramidase
LPIN1 lipin 1
NDRG1 N-myc downstream regulated 1
NMNAT2 nicotinamide nucleotide adenylyltransferase 2
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SCYL1 SCY1-like 1 (S. cerevisiae)
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6