Gene table: search width pubmed_id = 10926541


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

protein
All allelic disease phenotypes - locus/disease symbols
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 2 - (AD)
16.35
10926541
SLC25A4 (4q35)
Mitochondrial carrier; adenine nucleotide translocator(M)
* Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal - PEOA2
* Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type) - MTDPS12A
* Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type) - MTDPS12B