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].
Latest Publications for our Kelch-like protein 41 抗体
du Puy, Beqqali, van Tol, Monshouwer-Kloots, Passier, Haagsman, Roelen: "Sarcosin (Krp1) in skeletal muscle differentiation: gene expression profiling and knockdown experiments." in: The International journal of developmental biology, Vol. 56, Issue 4, pp. 301-9, (2012) (PubMed).
Aliases for Kelch-like protein 41 抗体
kelch-like 41 (Klhl41) 抗体 kelch-like family member 41 (Klhl41) 抗体 kelch like family member 41 (KLHL41) 抗体 kelch like family member 41 L homeolog (klhl41.L) 抗体 kelch-like family member 41b (klhl41b) 抗体 cb52 抗体 Gm112 抗体 Kbtbd10 抗体 KBTBD10 抗体 kbtbd10 抗体 kbtbd10b 抗体 klhl41 抗体 Krp1 抗体 SARCOSIN 抗体 Sarcosin 抗体 sarcosin 抗体 sb:cb52 抗体 wu:fb24f05 抗体 wu:fc15e07 抗体