Your search for "hydin" returned 156 TaqMan® SNP Genotyping Assays
HYDIN, axonemal central pair apparatus protein
This gene encodes a protein that may be involved in cilia motility. Mutations in this gene cause of autosomal recessive primary ciliary dyskinesia-5, a disorder characterized by the accumulation of cerebrospinal fluid within the ventricles of the brain. A duplicate copy of this gene has been found in humans on chromosome 1. [provided by RefSeq, Jan 2013]
1700034M11RIK, 4930545D19RIK, 4932703P14, A830061H17, AC069308.21GM4, CILD5, HY-3, HY3, HYDIN, HYDIN1, HYDIN2, HYRH, PPP1R31
(Human) Q4G0P3, (Human) A6NC70, (Human) A6NLZ0, (Human) B4DQY4, (Human) B4DRN4, (Human) F5H6V3, (Human) Q8N3H8, (Human) Q8N3P6, (Human) Q8TC08, (Human) Q96JG3, (Human) Q96SS4, (Human) Q9H5U3, (Human) Q9H9B8, (Human) Q9NTI0, (Human) Q9UBE5, (Mouse) Q80W93, (Mouse) Q3UQ06, (Mouse) Q68ED1, (Mouse) Q8BRL9, (Mouse) Q8CDF4
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