Gene table: search width pubmed_id = 31463572


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Congenital muscular dystrophy related to MSTO1 - (AR)
2.49
28544275
31130378
31463572
MSTO1 (1q22)
Misato homolog 1 (Drosophila)(M)
* Myopathy, mitochondrial and cerebellar ataxia - MMYAT