Hydrocephalus Inducing 抗体
(Hydrocephalus Inducing (HYDIN))
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].
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Aliases for Hydrocephalus Inducing 抗体
HYDIN, axonemal central pair apparatus protein (hydin) 抗体HYDIN, axonemal central pair apparatus protein (Hydin) 抗体
Hydin, axonemal central pair apparatus protein (Hydin) 抗体
HYDIN, axonemal central pair apparatus protein (HYDIN) 抗体
1700034M11Rik 抗体
4930545D19Rik 抗体
4932703P14 抗体
A830061H17 抗体
AC069308.21gm4 抗体
CILD5 抗体
hy-3 抗体
hy3 抗体
HYDIN1 抗体
HYDIN2 抗体
hyrh 抗体
PPP1R31 抗体
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