Gene: MSTO1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55154
Gene Symbol: MSTO1
MSTO1 		0.110 GeneticVariation phenotype BEFREE Recently, MSTO1 mutations have been shown to cause clinical manifestations suggestive of mitochondrial dysfunction, such as muscle weakness, short stature, motor developmental delay, and cerebellar atrophy. 29339779 2018
Entrez Id: 55154
Gene Symbol: MSTO1
MSTO1 		0.110 Biomarker phenotype HPO