Your search for "spg11" returned 305 TaqMan® SNP Genotyping Assays
spastic paraplegia 11 (autosomal recessive)
The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
6030465E24RIK, A330015I11, ALS5, C530005A01RIK, CMT2X, KIAA1840, RGD1562529, SPG11
(Human) Q96JI7, (Human) A8KAX9, (Human) B9EK60, (Human) F5H3N6, (Human) Q4VC11, (Human) Q58G86, (Human) Q69YG6, (Human) Q6NW01, (Human) Q8N270, (Human) Q8TBU9, (Human) Q9H734, (Mouse) Q3UHA3, (Mouse) A2ARM0, (Mouse) Q6ZPH3, (Mouse) Q8BHQ1, (Mouse) Q8C7R3, (Mouse) Q8C7U2, (Mouse) Q8CA88, (Mouse) Q8VEA5
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