LRP11: LDL Receptor Related Protein 11

A member of the low-density lipoprotein receptor family involved in endocytosis and signaling

Gene Information Card

Symbol LRP11
Full Name LDL Receptor Related Protein 11
Gene Type protein-coding
Chromosomal Location 6q25.1
NCBI Gene ID 84918 ncbi.nlm.nih.gov/gene/84918
Ensembl ID ENSG00000124782
UniProt ID Q5T7N2
OMIM ID 610764
HGNC ID 19689
Aliases MGC14836, bA350J20.1

Description

LRP11 (LDL Receptor Related Protein 11) is a protein-coding gene belonging to the low-density lipoprotein receptor family. The encoded protein is involved in receptor-mediated endocytosis and may play a role in lipid metabolism and cellular signaling. LRP11 is expressed in multiple tissues and has been implicated in various cancers and metabolic disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Hepatocellular carcinoma Altered LRP11 expression may affect lipoprotein uptake and signaling pathways in hepatocytes PMID: 25691885
Colorectal cancer LRP11 overexpression correlates with tumor progression and poor prognosis PMID: 29228537
Alzheimer's disease LRP11 may modulate amyloid-beta clearance via LRP family interactions PMID: 23382691

Expression Profile

Tissue Expression
Tissue nTPM level
Liver 12.5 Medium
Kidney 8.3 Medium
Lung 6.1 Low
Brain 4.7 Low
Heart 3.2 Low
Cell Line Expression
Cell Line nTPM Notes
HepG2 15.0 Hepatocellular carcinoma cell line
A549 7.8 Lung adenocarcinoma cell line
HEK293 5.4 Embryonic kidney cells
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1234C>T Missense 0.01% p.Pro412Ser; predicted benign
c.567G>A Nonsense <0.01% p.Trp189*; loss of function
c.890_891insA Frameshift 0.005% p.Thr297fs; truncated protein
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations (e.g., p.Trp189*, p.Thr297fs) lead to premature termination and loss of LRP11 function.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in LRP11.

Dominant Negative (DN)

No evidence of dominant-negative effects for LRP11 mutations.

Pathways

• Endocytosis (KEGG: hsa04144)
• Lipoprotein metabolism (Reactome: R-HSA-174824)

Protein Summary

LRP11 encodes a 777-amino acid type I transmembrane protein with multiple ligand-binding repeats characteristic of the LDL receptor family. The protein localizes to the plasma membrane and mediates endocytosis of lipoprotein particles. It is expressed in liver, kidney, and other tissues, and its dysregulation is associated with cancer and neurodegenerative diseases.

Related Products

Product name Cat.No. Species Gene ID
LRP11 Knockout HEK293 Cell Line EDJ-KQ3274 Human 84918 Details Get a Quote
LRP11 Knockout A-549 Cell Line EDJ-KQ24822 Human 84918 Details Get a Quote
LRP11 Knockout HCT 116 Cell Line EDJ-KQ24823 Human 84918 Details Get a Quote
LRP11 Knockout HeLa Cell Line EDJ-KQ24824 Human 84918 Details Get a Quote
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