Gene: MRPS2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51116
Gene Symbol: MRPS2
MRPS2 		0.110 Biomarker disease BEFREE Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies. 29576219 2018
Entrez Id: 51116
Gene Symbol: MRPS2
MRPS2 		0.110 Biomarker disease HPO