Gene table: search width pubmed_id = 30452684


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Combined oxidative phosphorylation deficiency 43 - (AR)
16.66
30452684
TIMM22 (17q13.3)
Translocase of inner mitochondrial membrane 22(M)
* Combined oxidative phosphorylation deficiency 43 - COXPD43