LMBRD1

Probable lysosomal cobalamin transporter is a protein that in humans is encoded by the LMBRD1 gene.[5][6]

LMBRD1
Identifiers
AliasesLMBRD1, C6orf209, LMBD1, MAHCF, NESI, LMBR1 domain containing 1
External IDsOMIM: 612625 MGI: 1915671 HomoloGene: 10156 GeneCards: LMBRD1
Gene location (Human)
Chr.Chromosome 6 (human)[1]
Band6q13Start69,672,757 bp[1]
End69,867,236 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

55788

68421

Ensembl

ENSG00000168216

ENSMUSG00000073725

UniProt

Q9NUN5

Q8K0B2

RefSeq (mRNA)

NM_018368
NM_001363722
NM_001367271
NM_001367272

NM_026719
NM_001310483

RefSeq (protein)

NP_060838
NP_001350651

NP_001297412
NP_080995

Location (UCSC)Chr 6: 69.67 – 69.87 MbChr 1: 24.68 – 24.77 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse


References

  1. GRCh38: Ensembl release 89: ENSG00000168216 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000073725 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Rutsch F, Gailus S, Miousse IR, Suormala T, Sagne C, Toliat MR, Nurnberg G, Wittkampf T, Buers I, Sharifi A, Stucki M, Becker C, Baumgartner M, Robenek H, Marquardt T, Hohne W, Gasnier B, Rosenblatt DS, Fowler B, Nurnberg P (Jan 2009). "Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism". Nat Genet. 41 (2): 234–9. doi:10.1038/ng.294. PMID 19136951.
  6. "Entrez Gene: LMBRD1 LMBR1 domain containing 1".

Further reading


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