Gene entry
CUBN
cubilin
- Chromosome
- 10
- Cytoband
- 10p13
- Variants (rsID)
- 137
CUBN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10p13). Its official name is “cubilin”. The reference table lists 137 variants (rsID) for this gene.
Clinically classified variants
34 reference-table entries with clinical significance.
- rs111265129Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs117035284Benignsingle nucleotide variantImerslund-Grasbeck syndrome|Imerslund-Grasbeck syndrome type 1
- rs12259370Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs12571671Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs140806389Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs1801223Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs1801225Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs1801228Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs1801230Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs1801231Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs1801238Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs1801239Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs2271460Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs2271462Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs2271468Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs2356590Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs3740165Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs41289303Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs41289311Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs41289313Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs45551835Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs703064Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs76789390Benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs117620008Conflicting interpretationssingle nucleotide variantImerslund-Grasbeck syndrome|Imerslund-Grasbeck syndrome type 1
- rs137998687Conflicting interpretationssingle nucleotide variantImerslund-Grasbeck syndrome
- rs141420691Likely benignsingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs386833787Likely pathogenicsingle nucleotide variantImerslund-Grasbeck syndrome
- rs121434430Pathogenicsingle nucleotide variantImerslund-Grasbeck syndrome|Imerslund-Grasbeck syndrome type 1
- rs386833771PathogenicDeletionImerslund-Grasbeck syndrome
- rs141089159Uncertain significancesingle nucleotide variantImerslund-Grasbeck syndrome
- rs150117913Uncertain significancesingle nucleotide variantImerslund-Grasbeck syndrome
- rs200593316Uncertain significancesingle nucleotide variantImerslund-Grasbeck syndrome type 1
- rs74844886Uncertain significancesingle nucleotide variantImerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome
- rs75386064Uncertain significancesingle nucleotide variantImerslund-Grasbeck syndrome
Other listed variants
- rs703062
- rs780805
- rs780807
- rs780821
- rs780825
- rs796667
- rs1512705
- rs1687716
- rs1891473
- rs1907358
- rs2137425
- rs2145939
- rs2172080
- rs2291521
- rs2356587
- rs2356825
- rs2796833
- rs2883972
- rs2942359
- rs2942366
- rs3012499
- rs3740169
- rs3847364
- rs4747288
- rs7071576
- rs7079269
- rs7089377
- rs7091547
- rs7097054
- rs7099855
- rs7894639
- rs7897550
- rs7900486
- rs7912716
- rs10752064
- rs10904839
- rs10904868
- rs11254244
- rs11254256
- rs11254262
- rs11254275
- rs11254322
- rs11254336
- rs11254339
- rs11254362
- rs11254363
- rs11254375
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.