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
Entrez Id: 340024
Gene Symbol: SLC6A19
SLC6A19 		0.610 Biomarker disease GENOMICS_ENGLAND A novel missense mutation in the SLC6A19 gene in a Chinese family with Hartnup disorder. 19335424 2009
Entrez Id: 340024
Gene Symbol: SLC6A19
SLC6A19 		0.610 GeneticVariation disease BEFREE Additional mutations were identified in the genes encoding the putative glycine transporter SLC6A18 (XT2) and the neutral amino acid transporter SLC6A19 (B0AT1) in families with either IG or HG, suggesting that mutations in the genes encoding these transporters may also contribute to these phenotypes. 19033659 2008
Entrez Id: 340024
Gene Symbol: SLC6A19
SLC6A19 		0.610 Biomarker disease CTD_human
Entrez Id: 340024
Gene Symbol: SLC6A19
SLC6A19 		0.610 Biomarker disease HPO
Entrez Id: 340024
Gene Symbol: SLC6A19
SLC6A19 		0.610 CausalMutation disease CLINVAR
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
Entrez Id: 5096
Gene Symbol: PCCB
PCCB 		0.100 Biomarker disease HPO
Entrez Id: 3712
Gene Symbol: IVD
IVD 		0.100 Biomarker disease HPO
Entrez Id: 8659
Gene Symbol: ALDH4A1
ALDH4A1 		0.100 Biomarker disease HPO
Entrez Id: 34
Gene Symbol: ACADM
ACADM 		0.100 Biomarker disease HPO
Entrez Id: 64087
Gene Symbol: MCCC2
MCCC2 		0.100 Biomarker disease HPO
Entrez Id: 2653
Gene Symbol: GCSH
GCSH 		0.100 Biomarker disease HPO
Entrez Id: 5095
Gene Symbol: PCCA
PCCA 		0.100 Biomarker disease HPO
Entrez Id: 275
Gene Symbol: AMT
AMT 		0.100 Biomarker disease HPO
Entrez Id: 2731
Gene Symbol: GLDC
GLDC 		0.100 Biomarker disease HPO
Entrez Id: 5625
Gene Symbol: PRODH
PRODH 		0.100 Biomarker disease HPO
Entrez Id: 348932
Gene Symbol: SLC6A18
SLC6A18 		0.010 Biomarker disease BEFREE Additional mutations were identified in the genes encoding the putative glycine transporter SLC6A18 (XT2) and the neutral amino acid transporter SLC6A19 (B0AT1) in families with either IG or HG, suggesting that mutations in the genes encoding these transporters may also contribute to these phenotypes. 19033659 2008