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HYDIN, HYDIN axonemal central pair apparatus protein

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  • Interaction Network
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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 »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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