MRPS22, mitochondrial ribosomal protein S22, 56945

N. diseases: 78; N. variants: 15
Disease: Muscle hypotonia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201337850
rs201337850
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22
CUI: C0026827
Disease:
Muscle hypotonia 		G 0.700 CausalMutation CLINVAR A patient with mitochondrial disorder due to a novel mutation in MRPS22. 28752220 2017
dbSNP: rs201337850
rs201337850
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22
CUI: C0026827
Disease:
Muscle hypotonia 		G 0.700 CausalMutation CLINVAR Whole exome sequencing in patients with white matter abnormalities. 27159321 2016
dbSNP: rs201337850
rs201337850
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22
CUI: C0026827
Disease:
Muscle hypotonia 		G 0.700 CausalMutation CLINVAR MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities. 25663021 2015
dbSNP: rs201337850
rs201337850
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22
CUI: C0026827
Disease:
Muscle hypotonia 		G 0.700 CausalMutation CLINVAR Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy. 21189481 2011
dbSNP: rs201337850
rs201337850
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22
CUI: C0026827
Disease:
Muscle hypotonia 		G 0.700 CausalMutation CLINVAR Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation. 17873122 2007