Gene table: search width pubmed_id = 1998334


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

protein
All allelic disease phenotypes - locus/disease symbols
Cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) - (XR)
10.103
1998334
8630491
TAZ (Xq28)
Tafazzin
* Barth syndrome - BTHS
* Endocardial fibroelastosis-2 - G4.5
* Noncompaction of left ventricular myocardium, isolated - INVM
* Cardiomyopathy, X-linked dilated - CMD3A