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LMBRD1 encodes a lysosomal membrane protein that may be involved in the transport and metabolism of cobalamin. Additionally we are shipping LMBR1 Domain Containing 1 Antibodies (12) and LMBR1 Domain Containing 1 Kits (1) and many more products for this protein.
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Results propose a model whereby membrane-bound LMBD1 and ABCD4 (show ABCD4 Proteins) facilitate the vectorial delivery of lysosomal vitamin B12 (show NDUFB3 Proteins) to cytoplasmic MMACHC (show MMACHC Proteins).
LMBD1 plays an imperative role in mediating and regulating the endocytosis of the IR.
These data indicate that by forming complexes with lamin A/C and nucleoporins, NESI facilitates the CRM1-independent nuclear export of large hepatitis delta antigen.
novel mutations in LMBRD1 in three patients
LMBRD1: the gene for the cblF defect of vitamin B metabolism.
a LMBRD1 mutation causes the cblF defect of vitamin B(12) metabolism in a Turkish patient [case report]
LMBRD1 is the gene underlying the cblF defect of cobalamin metabolism and suggests that LMBD1 is a lysosomal membrane exporter for cobalamin.
This gene encodes a lysosomal membrane protein that may be involved in the transport and metabolism of cobalamin. This protein also interacts with the large form of the hepatitis delta antigen and may be required for the nucleocytoplasmic shuttling of the hepatitis delta virus. Mutations in this gene are associated with the vitamin B12 metabolism disorder termed, homocystinuria-megaloblastic anemia complementation type F.
LMBR1 domain-containing protein 1
, probable lysosomal cobalamin transporter
, LMBR1 domain containing 1
, HDAg-L-interacting protein NESI
, hepatitis delta antigen-L interacting protein
, liver regeneration p-53 related protein
, nuclear export signal-interacting protein
, protein N90b