HYDIN, HYDIN axonemal central pair apparatus protein

HYDIN, 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]

• Gene Synonyms (hydrocephalus-inducing protein homolog, protein phosphatase 1, regulatory subunit 31, CILD5, HYDIN1, HYDIN2, PPP1R31,)
• NCBI Gene ID: 54768
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q4G0P3
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

HYDIN axonemal central pair apparatus protein interacts with:

• penta-EF-hand domain containing 1

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.