Gene table: search width pubmed_id = 36823193


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

protein
All allelic disease phenotypes - locus/disease symbols
Combined oxidative phosphorylation deficiency 58 - (AR)
17.54
36823193
TEFM (17q11.2 )
Transcription elongation factor, mitochondrial(M)
* Congenital myasthenic syndrome
* Combined oxidative phosphorylation deficiency 58 - COXPD58