{{Rsnum
|rsid=386834022
|Chromosome=1
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=POMGNT1
|position=46189477
|Gene_s=POMGNT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000050004.1
|CLNALLE=1
|CLNDBN=Muscle eye brain disease
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1291:C0457133:253280:ORPHA588:ORPHA899:277950001
|CLNHGVS=NC_000001.11:g.46189477delC
|CLNSIG=4
|Disease=Muscle eye brain disease
|FwdREF=G
|REF=AC
|RSPOS=46189476
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;NSF;REF;INT;ASP;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068081205000002110200
|WGT=1
|dbSNPBuildID=137
|rsid=386834022
|GENEINFO=POMGNT1:55624
|GENE_ID=55624
|GENE_NAME=POMGNT1
|CLNORIGIN=0
|CLNSRC=ClinVar
|CLNSRCID=NM_001243766.1:c.1869+7delG; NM_017739.3:c.1876delG
}}{{PMID Auto
|PMID=11709191
|Title=Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.
}}