Gene table: search width pubmed_id = 12474143


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

protein
All allelic disease phenotypes - locus/disease symbols
Cardio-encephalo-myopathy, fatal infantile, related to SCO2
10.35
12474143
SCO2 (22q13.33)
Cytochrome c oxidase assembly protein(M)
* Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 - CEMCOX1
* Charcot-Marie-Tooth disease, axonal, related to SCO2