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This gene encodes a ciliary outer dynein arm protein and is a member of the dynein heavy chain family. It is a microtubule-dependent motor ATPase and has been reported to be involved in the movement of respiratory cilia. Mutations in this gene have been implicated in causing Kartagener Syndrome (a combination of situs inversus totalis and Primary Ciliary Dyskinesia (PCD), also called Immotile Cilia Syndrome 1 (ICS1)) and male sterility. [provided by RefSeq, Mar 2013].
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Protein Aliases: Axonemal beta dynein heavy chain 11; axonemal dynein heavy chain 11; Ciliary dynein heavy chain 11; Dynein axonemal heavy chain 11; dynein, axonemal, heavy chain 11; dynein, axonemal, heavy polypeptide 11; dynein, ciliary, heavy chain 11
Gene Aliases: CILD7; DNAH11; DNAHBL; DNAHC11; DNHBL; DPL11
UniProt ID: (Human) Q96DT5
Entrez Gene ID: (Human) 8701
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