RASD2 FISH Probe

This gene belongs to the Ras superfamily of small GTPases and is enriched in the striatum. The encoded protein functions as an E3 ligase for attachment of small ubiquitin-like modifier (SUMO). This protein also binds to mutant huntingtin (mHtt), the protein mutated in Huntington disease (HD). Sumoylation of mHTT by this protein may cause degeneration of the striatum. The protein functions as an activator of mechanistic target of rapamycin 1 (mTOR1), which in turn plays a role in myelination, axon growth and regeneration. Reduced levels of mRNA expressed by this gene were found in HD patients. [provided by RefSeq, Jan 2016]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
RASD2-20-RE 20 (40 μL) 200 μL color Request Pricing
RASD2-20-OR 20 (40 μL) 200 μL color Request Pricing
RASD2-20-GO 20 (40 μL) 200 μL color Request Pricing
RASD2-20-GR 20 (40 μL) 200 μL color Request Pricing
RASD2-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

This gene belongs to the Ras superfamily of small GTPases and is enriched in the striatum. The encoded protein functions as an E3 ligase for attachment of small ubiquitin-like modifier (SUMO). This protein also binds to mutant huntingtin (mHtt), the protein mutated in Huntington disease (HD). Sumoylation of mHTT by this protein may cause degeneration of the striatum. The protein functions as an activator of mechanistic target of rapamycin 1 (mTOR1), which in turn plays a role in myelination, axon growth and regeneration. Reduced levels of mRNA expressed by this gene were found in HD patients. [provided by RefSeq, Jan 2016]

Gene Details

Gene Symbol : RASD2

Gene Name : RASD family member 2

Chromosome : CHR 22: 355,404,91-355,540,02

Locus : 22q12.3

Alt. Genes : HNRNPA3P1

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