OXA1L OXA1L mitochondrial inner membrane protein [ Homo sapiens (human) ] - Gene - Data resources

5018

OXA1L OXA1L mitochondrial inner membrane protein [ Homo sapiens (human) ]
Source: NCBI Gene (ID 5018)

Symbol: OXA1L

Full name: OXA1L mitochondrial inner membrane protein

Gene type: protein coding

RefSeq status: REVIEWED

Also known as: OXA1; OXA1L1

Summary: This gene encodes an evolutionarily conserved protein that is localized to the inner mitochondrial membrane. The encoded protein is essential for the translocation of the N-terminal tail of subunit 2 of cytochrome c oxidase, and is involved in the assembly of the cytochrome c oxidase and ATPase complexes of the mitochondrial respiratory chain. [provided by RefSeq, Jul 2016]

Expression: Ubiquitous expression in heart (RPKM 54.4), duodenum (RPKM 53.5) and 25 other tissues

Orthologs: mouse

Gene size: 6355bp

Exon count: 10