Your search for "plekhg5" returned 218 TaqMan® SNP Genotyping Assays
pleckstrin homology and RhoGEF domain containing G5
This gene encodes a protein that activates the nuclear factor kappa B (NFKB1) signaling pathway. Mutations in this gene are associated with autosomal recessive distal spinal muscular atrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]
BC023181, CMTRIC, DSMA4, GEF720, PLEKHG5, SYX, TECH
(Human) O94827, (Human) B3KU07, (Human) B7Z2M3, (Human) B7Z5X2, (Human) F5GZ21, (Human) F5H1I0, (Human) Q5SY17, (Human) Q5T8W5, (Human) Q5T8W9, (Human) Q6ZNM0, (Human) Q7Z436, (Human) Q86YD8, (Human) Q96BS1, (Mouse) Q66T02, (Mouse) A2A8B6, (Mouse) A2A8B7, (Mouse) Q66T00, (Mouse) Q6P3B1, (Mouse) Q6ZQ62, (Mouse) Q8R571, (Rat) Q6RFZ7
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