NP_001185471.1
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
105,338 Da
NCBI Official Full Name
hydrocephalus-inducing protein homolog isoform c
NCBI Official Synonym Full Names
HYDIN, axonemal central pair apparatus protein
NCBI Protein Information
hydrocephalus-inducing protein homolog
UniProt Protein Name
Hydrocephalus-inducing protein homolog
UniProt Synonym Gene Names
UniProt Entry Name
HYDIN_HUMAN
NCBI Summary for 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]
UniProt Comments for HYDIN
HYDIN: 5 isoforms of the human protein are produced by alternative splicing.
Chromosomal Location of Human Ortholog: 16q22.2
Biological Process: epithelial cell development; ventricular system development
Disease: Ciliary Dyskinesia, Primary, 5
Research Articles on HYDIN
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Diseases associated with anti-HYDIN antibody
Organs/Tissues associated with anti-HYDIN antibody
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