Gene table: search width pubmed_id = 23929671


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 oxydative phosphorylation deficiency 10 - (AR)
10.36
22608499
23929671
MTO1 (6q13)
Mitochondrial tRNA translation optimization 1(M)
* Mitochondrial hypertrophic cardiomyopathy related to MTO1 - COXPD10