Your search for "whsc1" returned 446 TaqMan® SNP Genotyping Assays
Wolf-Hirschhorn syndrome candidate 1
This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences. [provided by RefSeq, Jul 2008]
5830445G22RIK, 9430010A17RIK, AW555663, C130020C13RIK, D030027O06RIK, D930023B08RIK, MKIAA1090, MMSET, NSD2, REIIBP, RGD1565590, TRX5, WHS, WHSC1, WHSC1L
(Human) O96028, (Human) A2A2T2, (Human) A2A2T3, (Human) A2A2T4, (Human) A7MCZ1, (Human) D3DVQ2, (Human) O96031, (Human) Q4VBY8, (Human) Q672J1, (Human) Q6IS00, (Human) Q86V01, (Human) Q9BZB4, (Human) Q9UI92, (Human) Q9UPR2, (Mouse) Q8BVE8, (Mouse) B3VCH6, (Mouse) Q6ZPY1, (Mouse) Q7TSF5, (Mouse) Q811F0
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