motor polyneuropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007178
Similar Terms
Downloads & Tools

Genes

5 genes associated with the motor polyneuropathy 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
GJC2 gap junction protein, gamma 2, 47kDa
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SPG11 spastic paraplegia 11 (autosomal recessive)
TRPV4 transient receptor potential cation channel, subfamily V, member 4