Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22 		0.700 Biomarker disease GENOMICS_ENGLAND Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development. 28425981 2017
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22 		0.700 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22 		0.700 GermlineCausalMutation disease ORPHANET Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation. 17873122 2007
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22 		0.700 Biomarker disease GENOMICS_ENGLAND Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation. 17873122 2007
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22 		0.700 GeneticVariation disease UNIPROT Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation. 17873122 2007
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22 		0.700 Biomarker disease CTD_human
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22 		0.700 CausalMutation disease CLINVAR