Gene: SLC36A2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 153201
Gene Symbol: SLC36A2
SLC36A2 		0.700 Biomarker disease GENOMICS_ENGLAND Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters. 19033659 2008
Entrez Id: 153201
Gene Symbol: SLC36A2
SLC36A2 		0.700 GeneticVariation disease UNIPROT Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters. 19033659 2008
Entrez Id: 153201
Gene Symbol: SLC36A2
SLC36A2 		0.700 Biomarker disease CTD_human
Entrez Id: 153201
Gene Symbol: SLC36A2
SLC36A2 		0.700 Biomarker disease HPO