Gene table: search width pubmed_id = 11687801


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

protein
All allelic disease phenotypes - locus/disease symbols
Mitochondrial DNA depletion myopathy - (AR)
16.33
11687801
TK2 (16q22-q23)
Thymidine kinase 2, mitochondrial(M)
* Mitochondrial dna depletion syndrome, myopathic form - MTDPS3
* Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive, 3 - PEOB3