Pages
Products

KIAA0196


Official Full Name
WASH complex subunit 5
Organism
Homo sapiens
Gene ID
9897
Background
This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases. [provided by RefSeq, Aug 2009]
Synonyms
WASHC5; RTSC; SPG8; RTSC1; KIAA0196

Cat.No. Product Name Price
SHH324507 shRNA set against Human KIAA0196 (NM_014846.3) Inquiry
Cat.No. Product Name Price
MiUTR1H-05203 KIAA0196 miRNA 3'UTR clone Inquiry
CDCB184157 Rabbit KIAA0196 ORF clone (XM_002710540.2) Inquiry
CDCR298364 Human KIAA0196 ORF Clone(NM_014846.3) Inquiry
CDCS418823 Human KIAA0196 ORF Clone (BC026951) Inquiry
Quick Inquiry