LMBRD1

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]

Description

LMBR1 domain containing 1

Protein family

Membrane proteins predicted by MDM, Transporters

Chromosome

6:q13 (70385694 - 70507003)

Ensembl ID

ENSG00000168216  (ver. 69.37)

Orthologs

Mouse Lmbrd1: ENSMUSG00000073725

Human splice variants
Mouse splice variants