Gene: SLC6A20 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54716
Gene Symbol: SLC6A20
SLC6A20 		0.600 Biomarker disease GENOMICS_ENGLAND Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters. 19033659 2008
Entrez Id: 54716
Gene Symbol: SLC6A20
SLC6A20 		0.600 Biomarker disease HPO
Entrez Id: 54716
Gene Symbol: SLC6A20
SLC6A20 		0.600 Biomarker disease CTD_human