{{Rsnum
|rsid=111033800
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=GALT
|position=34649502
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GALT
}}{{omim
|id=606999
|rsnum=111033800
|variant=0002
}}
{{omim
|id=606999
|rsnum=111033800
|variant=0015
}}{{ClinVar
|rsid=111033800
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=34649499
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=GALT:2592
|GENE_NAME=GALT
|GENE_ID=2592
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000009.11:g.34649499C>G; NC_000009.11:g.34649499C>T
|CLNSRC=OMIM Allelic Variant; Emory University
|CLNORIGIN=1
|CLNSRCID=606999.0015; 771; 606999.0002
|CLNSIG=5
|CLNCUI=C0268151; C0268151,C0268151
|CLNDBN=Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase; not provided
|Disease=Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase; not provided
|CLNACC=RCV000003807.1; RCV000003794.1; RCV000078246.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1518:C0268151:230400:352:79239:124354006
}}{{PMID Auto
|PMID=7550229
|Title=Molecular characterization of galactosemia (type 1) mutations in Japanese.
}}

{{PMID Auto
|PMID=8692963
|Title=Heterodimer formation and activity in the human enzyme galactose-1-phosphate uridylyltransferase.
|OA=1
}}

{{PMID Auto
|PMID=8892021
|Title=Molecular characterization of Duarte-1 and Duarte-2 variants of galactose-1-phosphate uridyltransferase.
}}

{{PMID Auto
|PMID=10573007
|Title=Molecular basis for phenotypic heterogeneity in galactosaemia: prediction of clinical phenotype from genotype in Japanese patients.
}}

{{PMID Auto
|PMID=20008339
|Title=Analysis of galactosemia-linked mutations of GALT enzyme using a computational biology approach.
}}

{{PMID Auto
|PMID=20547145
|Title=Molecular and biochemical characterization of the GALT gene in Korean patients with galactose-1-phosphate uridyltransferase deficiency.
}}