DISEASES

Disease-gene associations mined from literature

Literature associating OXA1L and mitochondrial metabolism disease

OXA1L [ENSP00000483491]

Mitochondrial inner membrane protein OXA1L; Required for the insertion of integral membrane proteins into the mitochondrial inner membrane. Essential for the activity and assembly of cytochrome oxidase. Required for the correct biogenesis of ATP synthase and complex I in mitochondria; Belongs to the OXA1/ALB3/YidC family.

Synonyms:  OXA1L,  OXA1Lp,  hOXA1L,  C9JC63,  E7EVY0 ...

Linkouts:  STRING  Pharos  UniProt