WASHC5 FISH Probe

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]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
WASHC5-20-RE 20 (40 μL) 200 μL color Request Pricing
WASHC5-20-OR 20 (40 μL) 200 μL color Request Pricing
WASHC5-20-GO 20 (40 μL) 200 μL color Request Pricing
WASHC5-20-GR 20 (40 μL) 200 μL color Request Pricing
WASHC5-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

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]

Gene Details

Gene Symbol : WASHC5

Gene Name : WASH complex subunit 5

Chromosome : CHR 8: 125,091,818-125,024,259

Locus : 8q24.13

Alt. Genes : ZNF263

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