Gene table: search width pubmed_id = 28295037


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Mitochondrial myopathy with severe neurological manifestations - (AR)
16.71
28295037
TMEM65 (8q24.13)
Transmembrane Protein 65
* Mitochondrial myopathy with severe neurological manifestations