Gene table: search width pubmed_id = 26541337


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

protein
All allelic disease phenotypes - locus/disease symbols
Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression - (AR)
16.57
26541337
SLC25A42 (19p13.11)
Solute carrier family 25 member 42(M)
* Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression - MECREN
* Mitochondrial myopathy