Your search for "kalrn" returned 2,362 TaqMan® SNP Genotyping Assays
kalirin, RhoGEF kinase
Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. [provided by RefSeq, Apr 2016]
2210407G14RIK, ARHGEF24, AV235988, CHD5, CHDS5, DUET, DUO, E530005C20RIK, GM539, HAPIP, KALIRIN, KALRN, TRAD
(Human) O60229, (Human) A8MSI4, (Human) C9JQ37, (Human) Q6ZN45, (Human) Q8TBQ5, (Human) Q9NSZ4, (Human) Q9Y2A5, (Mouse) A2CG49, (Mouse) A2CG50, (Mouse) A2CG51, (Mouse) A2CG52, (Mouse) A2CG53, (Mouse) B2RXR5, (Mouse) Q3TXY8, (Mouse) Q3TYL1, (Mouse) Q3UTA5, (Mouse) Q8BTT9, (Mouse) Q8C4Q2, (Mouse) Q9CVA9, (Rat) P97924, (Rat) O70135, (Rat) Q6IV51, (Rat) Q9JIF1, (Rat) Q9JIF2, (Rat) Q9JIG0, (Rat) Q9JIH3
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