{{Rsnum
|rsid=386833782
|Chromosome=10
|position=17046533
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CUBN
|Gene_s=CUBN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=C
|CHROM=10
|CLNACC=RCV000050203.1
|CLNALLE=1
|CLNDBN=Megaloblastic anemia due to inborn errors of metabolism
|CLNDSDB=MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1306856:250950:261100:35858:34925000
|CLNHGVS=NC_000010.10:g.17088532G>C
|CLNSIG=4
|Disease=Megaloblastic anemia due to inborn errors of metabolism
|FwdALT=G
|FwdREF=C
|REF=G
|RSPOS=17088532
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833782
|GENEINFO=CUBN:8029
|GENE_ID=8029
|GENE_NAME=CUBN
}}{{PMID Auto
|PMID=10080186
|Title=Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1.
}}

{{PMID Auto
|PMID=15024727
|Title=Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East.
}}

{{PMID Auto
|PMID=22929189
|Title=Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.
|OA=1
}}