LMBRD1

LMBRD1
Identifiers
Aliases	LMBRD1, C6orf209, LMBD1, MAHCF, NESI, LMBR1 domain containing 1
External IDs	OMIM: 612625; MGI: 1915671; HomoloGene: 10156; GeneCards: LMBRD1; OMA:LMBRD1 - orthologs
Gene location (Human)
Chr.	Chromosome 6 (human)
End	69,867,236 bp
Gene location (Mouse)
Chr.	Chromosome 1 (mouse)
End	24,805,382 bp
RNA expression pattern
	Top expressed in
	secondary oocyte; ; retinal pigment epithelium; ; islet of Langerhans; ; olfactory bulb; ; bronchial epithelial cell; ; corpus callosum; ; C1 segment; ; Epithelium of choroid plexus; ; skin of thigh; ; cerebellar vermis;
	Top expressed in
	saccule; ; ectoderm; ; otic vesicle; ; otic placode; ; spermatid; ; Epithelium of choroid plexus; ; neural layer of retina; ; superior frontal gyrus; ; stroma of bone marrow; ; anterior horn of spinal cord;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	cobalamin binding; insulin receptor binding; ABC-type vitamin B12 transporter activity;
Cellular component	integral component of membrane; clathrin-coated endocytic vesicle; lysosomal membrane; plasma membrane; lysosome; membrane;
Biological process	cobalamin metabolic process; insulin receptor internalization; negative regulation of glucose import; negative regulation of insulin receptor signaling pathway; negative regulation of protein kinase B signaling; viral process; cobalamin transport; transport;
	Sources:Amigo / QuickGO
Orthologs
	55788
	68421
	ENSG00000168216
	ENSMUSG00000073725
	Q9NUN5
	Q8K0B2
	NM_018368; NM_001363722; NM_001367271; NM_001367272
	NM_026719; NM_001310483
	NP_060838; NP_001350651
	NP_001297412; NP_080995
	Wikidata
View/Edit Human	View/Edit Mouse

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