×
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
×
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:
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:
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:
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