OXA1L

OXA1L mitochondrial inner membrane protein

HCNC Approved Symbol

OXA1L (HGNC:8526)

Genomic Coordinates

14:22,766,688 - 22,773,042 (14q11.2)

Synonyms

MGC133129, OXA1, OXA1L1

Disease Associations

Currently, this gene is not associated with any human disease in OMIM.
However, the following publication(s) suggest a possible gene disease association.

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ContentsPublications

OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect.

PMID:30201738