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Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
Kintoun, is a protein that is encoded by the DNAAF2 gene.[5][6]
DNAAF2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | DNAAF2, C14orf104, CILD10, KTU, PF13, dynein (axonemal) assembly factor 2, dynein axonemal assembly factor 2 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 612517; MGI: 1923566; HomoloGene: 10026; GeneCards: DNAAF2; OMA:DNAAF2 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Kintoun is a highly conserved protein involved in the preassembly of dynein arm complexes which power cilia. These complexes are found in some cilia and are assembled in the cytoplasm prior to transport for ciliogenesis.[5]
Mutations in DNAAF2 are associated with primary ciliary dyskinesia.[7]
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