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HYDIN is 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.
Gene Name: | HYDIN, axonemal central pair apparatus protein |
Synonyms: | HYDIN, CILD5, Hydrocephalus inducing, HYDIN2, Hydrocephalus inducing homolog, KIAA1864, HYDIN1, PPP1R31 |
Target Sequences: | NM_017558 NP_060028.2 Q4G0P3 |
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