Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 65080
Gene Symbol: MRPL44
MRPL44 		0.700 GermlineCausalMutation disease ORPHANET Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy. 23315540 2013
Entrez Id: 65080
Gene Symbol: MRPL44
MRPL44 		0.700 Biomarker disease GENOMICS_ENGLAND Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy. 23315540 2013
Entrez Id: 65080
Gene Symbol: MRPL44
MRPL44 		0.700 GeneticVariation disease UNIPROT Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy. 23315540 2013
Entrez Id: 65080
Gene Symbol: MRPL44
MRPL44 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 65080
Gene Symbol: MRPL44
MRPL44 		0.700 CausalMutation disease CLINVAR
Entrez Id: 65080
Gene Symbol: MRPL44
MRPL44 		0.700 Biomarker disease CTD_human