Gene table: search width pubmed_id = 21931170


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
Mitochondrial complex 1 deficiency, nuclear type 11 - (AD)
10.32
21931170
NDUFAF1 (15q15.1)
NADH-ubiquinone oxidoreductase 1 alpha subcomplex(M)
* patient with HCM and isolated respiratory complex I deficiency
* Hypertrophic mitochondrial cardiomyopathy related to NDUFAF1
* Mitochondrial complex 1 deficiency, nuclear type 11 - MC1DN11