{{Rsnum
|rsid=36007394
|Chromosome=12
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=GNPTAB
|Gene_s=GNPTAB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=101766123
}}{{ClinVar
|ALT=A
|CHROM=12
|CLNACC=RCV000031968.2
|CLNALLE=1
|CLNDBN=I cell disease
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1828:NBK1875:C2673377:252500:576
|CLNHGVS=NC_000012.11:g.102159901delG
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1875
|Disease=I cell disease
|FwdREF=C
|GENEINFO=GNPTAB:79158
|GENE_ID=79158
|GENE_NAME=GNPTAB
|REF=AG
|RSPOS=102159899
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;VLD;GNO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000040102110200
|WGT=0
|dbSNPBuildID=126
|rsid=36007394
}}{{PMID Auto
|PMID=16465621
|Title=Mucolipidosis II (I-cell disease) and mucolipidosis IIIA (classical pseudo-hurler polydystrophy) are caused by mutations in the GlcNAc-phosphotransferase alpha / beta -subunits precursor gene.
|OA=1
}}