LRP6 LDL receptor related protein 6
Gene ID: 4040, updated on 2-Nov-2024Gene type: protein coding
Also known as: ADCAD2; STHAG7
- See all available tests in GTR for this gene
- Go to complete Gene record for LRP6
- Go to Variation Viewer for LRP6 variants
Summary
This gene encodes a member of the low density lipoprotein (LDL) receptor gene family. LDL receptors are transmembrane cell surface proteins involved in receptor-mediated endocytosis of lipoprotein and protein ligands. The protein encoded by this gene functions as a receptor or, with Frizzled, a co-receptor for Wnt and thereby transmits the canonical Wnt/beta-catenin signaling cascade. Through its interaction with the Wnt/beta-catenin signaling cascade this gene plays a role in the regulation of cell differentiation, proliferation, and migration and the development of many cancer types. This protein undergoes gamma-secretase dependent RIP- (regulated intramembrane proteolysis) processing but the precise locations of the cleavage sites have not been determined.[provided by RefSeq, Dec 2009]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Coronary artery disease, autosomal dominant 2 | See labs |
Genetics of coronary artery calcification among African Americans, a meta-analysis. GeneReviews: Not available | |
Tooth agenesis, selective, 7 | See labs |
Genomic context
- Location:
- 12p13.2
- Sequence:
- Chromosome: 12; NC_000012.12 (12116025..12267044, complement)
- Total number of exons:
- 29
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for LRP6 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- LRP6 database
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.