{"symbol":"KLHL41","synonyms":["SARCOSIN","KRP1","KBTBD10"],"name":"kelch-like family member 41","description":"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]","ncbiEntrezGeneId":10324,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/10324","proteins":[{"symbol":"KLH41_HUMAN","href":"/api/1.0/protein/KLH41_HUMAN"}],"hgncRootFamilies":[{"name":"Kelch-like (KLHL)","href":"/api/1.0/gene_family/Kelch-like+%28KLHL%29"},{"name":"BTB (POZ) domain containing (BTBD)","href":"/api/1.0/gene_family/BTB+%28POZ%29+domain+containing+%28BTBD%29"}]}