spinal cord 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 spinal cord (Mammalian Phenotype Ontology, MP_0012712)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012712
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Genes

1 gene mutations causing the spinal cord degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6