Mus musculus Gene: Lrp2
Summary
InnateDB Gene IDBG-176227.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Lrp2
Gene Name low density lipoprotein receptor-related protein 2
Synonyms AI315343; AW536255; b2b1625.2Clo; D230004K18Rik; Gp330; Megalin
Species Mus musculus
Ensembl Gene ENSMUSG00000027070
Encoded Proteins
low density lipoprotein receptor-related protein 2
low density lipoprotein receptor-related protein 2
low density lipoprotein receptor-related protein 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000081479:
The protein encoded by this gene, low density lipoprotein-related protein 2 (LRP2) or megalin, is a multi-ligand endocytic receptor that is expressed in many different tissues but primarily in absorptive epithilial tissues such as the kidney. This glycoprotein has a large amino-terminal extracellular domain, a single transmembrane domain, and a short carboxy-terminal cytoplasmic tail. The extracellular ligand-binding-domains bind diverse macromolecules including albumin, apolipoproteins B and E, and lipoprotein lipase. The LRP2 protein is critical for the reuptake of numerous ligands, including lipoproteins, sterols, vitamin-binding proteins, and hormones. This protein also has a role in cell-signaling; extracellular ligands include parathyroid horomones and the morphogen sonic hedgehog while cytosolic ligands include MAP kinase scaffold proteins and JNK interacting proteins. Recycling of this membrane receptor is regulated by phosphorylation of its cytoplasmic domain. Mutations in this gene cause Donnai-Barrow syndrome (DBS) and facio-oculoacoustico-renal syndrome (FOAR).[provided by RefSeq, Aug 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:69424340-69586065
Strand Reverse strand
Band C2
Transcripts
ENSMUST00000080953 ENSMUSP00000079752
ENSMUST00000100051 ENSMUSP00000097628
ENSMUST00000092551 ENSMUSP00000090212
ENSMUST00000128742
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
They are also associated with 35 interaction(s) predicted by orthology.
Experimentally validated
Total 9 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 35 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004872 receptor activity
GO:0005509 calcium ion binding
GO:0005515 protein binding
GO:0017124 SH3 domain binding
Biological Process
GO:0006766 vitamin metabolic process
GO:0006898 receptor-mediated endocytosis
GO:0008283 cell proliferation
GO:0030900 forebrain development
Cellular Component
GO:0005765 lysosomal membrane
GO:0005768 endosome
GO:0005783 endoplasmic reticulum
GO:0005794 Golgi apparatus
GO:0005903 brush border
GO:0005905 coated pit
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0016324 apical plasma membrane
GO:0030139 endocytic vesicle
GO:0031526 brush border membrane
GO:0043235 receptor complex
GO:0045177 apical part of cell
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Disease pathway
Retinoid metabolism and transport pathway
Vitamin D (calciferol) metabolism pathway
Metabolism pathway
Metabolism of lipids and lipoproteins pathway
Visual phototransduction pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
Metabolism of steroid hormones and vitamin D pathway
KEGG
Hedgehog signaling pathway pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Retinoid metabolism and transport pathway
Vitamin D (calciferol) metabolism pathway
Metabolism of lipids and lipoproteins pathway
Metabolism of steroid hormones and vitamin D pathway
Signal Transduction pathway
Diseases associated with visual transduction pathway
Visual phototransduction pathway
Metabolism pathway
Disease pathway
KEGG
Hedgehog signaling pathway pathway
INOH
PID NCI
Signaling events mediated by the Hedgehog family
Cross-References
SwissProt A2ARV4
TrEMBL A2ARV5 Q3V346
UniProt Splice Variant
Entrez Gene 14725
UniGene Mm.23847 Mm.412822 Mm.447765
RefSeq NM_001081088
OMIM
CCDS CCDS38135
HPRD
IMGT
MGI ID MGI:95794
MGI Symbol Lrp2
EMBL AF197160 AK049346 AK166702 AL845489 Y08566
GenPept AAF61488 BAE38957 BAE43341 CAA69877 CAM20178
RNA Seq Atlas 14725