Jump to content

LMBRD1

From Wikipedia, the free encyclopedia

This is the current revision of this page, as edited by 1234qwer1234qwer4 (talk | contribs) at 23:25, 3 March 2023 (Importing Wikidata short description: Protein-coding gene in the species Homo sapiens (shortdescs-in-category)). The present address (URL) is a permanent link to this version.

(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)
LMBRD1
Identifiers
AliasesLMBRD1, C6orf209, LMBD1, MAHCF, NESI, LMBR1 domain containing 1
External IDsOMIM: 612625; MGI: 1915671; HomoloGene: 10156; GeneCards: LMBRD1; OMA:LMBRD1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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: 24.72 – 24.81 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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


References

[edit]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000168216Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000073725Ensembl, 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. S2CID 28006539.
  6. ^ "Entrez Gene: LMBRD1 LMBR1 domain containing 1".

Further reading

[edit]
[edit]