Gene: MRPS14 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 63931
Gene Symbol: MRPS14
MRPS14 		0.110 GeneticVariation phenotype BEFREE A variant in MRPS14 (uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement. 30358850 2019
Entrez Id: 63931
Gene Symbol: MRPS14
MRPS14 		0.110 Biomarker phenotype HPO