Probable lysosomal cobalamin transporter is a protein that in humans is encoded by the LMBRD1 gene.
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.[provided by RefSeq, Oct 2009].
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Probable lysosomal cobalamin transporter is a protein that in humans is encoded by the LMBRD1 gene.
==References==
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).