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KBTBD10

Official Full Name
kelch like family member 41
Organism
Homo sapiens
GeneID
10324
Background
This gene is a member of the kelch-like family. The encoded protein contains a BACK domain, a BTB/POZ domain, and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM), a rare congenital muscle disorder. [provided by RefSeq, Mar 2015]
Synonyms
KLHL41; Krp1; KBTBD10; SARCOSIN;

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