KLHL41 kelch like family member 41 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 10324)
Symbol: KLHL41
Full name: kelch like family member 41
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: KBTBD10; Krp1; SARCOSIN
Summary: 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]
Expression: Biased expression in prostate (RPKM 65.0), esophagus (RPKM 43.9) and 2 other tissues
Orthologs: mouse
Gene size: 16557bp
Exon count: 6