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HYDIN

Official Full Name
HYDIN axonemal central pair apparatus protein
Organism
Homo sapiens
GeneID
54768
Background
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]
Synonyms
CILD5; HYDIN1; HYDIN2; PPP1R31;

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