KLHL41, kelch like family member 41

KLHL41, kelch like family member 41

• 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]

• Gene Synonyms (KBTBD10, Krp1, SARCOSIN, kelch-like protein 41, kel-like protein 23, kelch repeat and BTB (POZ) domain containing 10, kelch-related protein 1, sarcomeric muscle protein,)
• NCBI Gene ID: 10324
• Species: Homo sapiens (Human)
• UNIPROT ID#>>O60662
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

kelch like family member 41 interacts with:

• chromosome 4 open reading frame 45
  kelch like family member 40
  kelch like family member 41
  ring finger and CHY zinc finger domain containing 1
  UTP11 small subunit processome component

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.