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LRP5 information


LRP5
Identifiers
AliasesLRP5, BMND1, EVR1, EVR4, HBM, LR3, LRP-5, LRP7, OPPG, OPS, OPTA1, VBCH2, LDL receptor related protein 5, PCLD4, LRP-7
External IDsOMIM: 603506 MGI: 1278315 HomoloGene: 1746 GeneCards: LRP5
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001291902
NM_002335

NM_008513

RefSeq (protein)

NP_001278831
NP_002326

NP_032539

Location (UCSC)Chr 11: 68.31 – 68.45 MbChr 19: 3.63 – 3.74 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Low-density lipoprotein receptor-related protein 5 is a protein that in humans is encoded by the LRP5 gene.[5][6][7] LRP5 is a key component of the LRP5/LRP6/Frizzled co-receptor group that is involved in canonical Wnt pathway. Mutations in LRP5 can lead to considerable changes in bone mass. A loss-of-function mutation causes osteoporosis pseudoglioma syndrome with a decrease in bone mass, while a gain-of-function mutation causes drastic increases in bone mass.

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000162337 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024913 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Hey PJ, Twells RC, Phillips MS, Brown SD, Kawaguchi Y, Cox R, Dugan V, Hammond H, Metzker ML, Todd JA, Hess JF (Aug 1998). "Cloning of a novel member of the low-density lipoprotein receptor family". Gene. 216 (1): 103–11. doi:10.1016/S0378-1119(98)00311-4. PMID 9714764.
  6. ^ Chen D, Lathrop W, Dong Y (Feb 1999). "Molecular cloning of mouse Lrp7(Lr3) cDNA and chromosomal mapping of orthologous genes in mouse and human". Genomics. 55 (3): 314–21. doi:10.1006/geno.1998.5688. PMID 10049586.
  7. ^ "Entrez Gene: LRP5 low density lipoprotein receptor-related protein 5".

and 22 Related for: LRP5 information

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LRP5

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the LRP5 gene. LRP5 is a key component of the LRP5/LRP6/Frizzled co-receptor group that is involved in canonical Wnt pathway. Mutations in LRP5 can lead...

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Serotonin

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V, et al. (March 2010). "Patients with high-bone-mass phenotype owing to Lrp5-T253I mutation have low plasma levels of serotonin". Journal of Bone and...

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LRP6

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that in humans is encoded by the LRP6 gene. LRP6 is a key component of the LRP5/LRP6/Frizzled co-receptor group that is involved in canonical Wnt pathway...

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Bone density

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Imperfecta COLIA2 Autosomal Recessive Osteoporosis Pseudoglioma Syndrome LRP5 Autosomal Recessive Osteopetrosis TCIRGI Autosomal Recessive Camurati-Engelmann...

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Osteogenesis imperfecta

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specifically more than any of the others. In the body, sclerostin binds to the LRP5 and LRP6 receptors, resulting in inhibition of the Wnt signaling pathway...

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Osteopetrosis

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Name OMIM Gene OPTA1 607634 LRP5 receptor OPTA2 166600 CLCN7 chloride channel OPTB1 259700 TCIRG1 ATPase OPTB2 259710 RANKL OPTB3 259730 CA2 (renal tubular...

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Worth syndrome

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LRP5 gene. It is characterized by increased bone density and benign bony structures on the palate. Worth syndrome is caused by a mutation in the LRP5...

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Wnt signaling pathway

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it to the proteasome to be digested. However, as soon as Wnt binds Fz and LRP5/6, the destruction complex function becomes disrupted. This is due to Wnt...

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Osteocyte

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sclerostin, a secreted protein that inhibits bone formation by binding to LRP5/LRP6 coreceptors and blunting Wnt signaling. Sclerostin, the product of the...

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Sclerostin

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antagonist. More recently, sclerostin has been identified as binding to LRP5/6 receptors and inhibiting the Wnt signaling pathway. The inhibition of the...

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Neurotransmitter

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Ryu JH, Suda N, Tanaka KF, Gingrich JA, Schütz G, et al. (November 2008). "Lrp5 controls bone formation by inhibiting serotonin synthesis in the duodenum"...

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Dickkopf

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protein 1 (DKK1). DKK proteins inhibit the Wnt signaling pathway coreceptors LRP5 and LRP6. They bind with high affinity as ligands to KREMEN1 and KREMEN2...

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IDDM11

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11p15.5 INS-VNTR IDDM3 15q26 D15S107 IDDM4 11q13 MDU1, ZFM1, RT6, FADD, LRP5 IDDM5 6q25 ESR, MnSOD IDDM6 18q12-q21 D18S487, D18S64, JK (Kidd locus) IDDM7...

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DKK1

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morphogenesis response to retinoic acid negative regulation of Wnt-Frizzled-LRP5/6 complex assembly positive regulation of heart induction by negative regulation...

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Zihai Li

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integrins,[excessive citations] Toll-like receptors (TLRs), Wnt co-receptors LRP5/6, the platelet receptor for the von Willebrand factor, and the latent TGFβ...

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Biochemical cascade

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non-canonical. The canonical signaling involves binding of Wnt to Frizzled and LRP5 co-receptor, leading to GSK3 phosphorylation and inhibition of β-catenin...

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Syndromic microphthalmia

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Oculodentodigital dysplasia (ODD) CPLANE1 AR Orofaciodigital syndrome type VI LRP5 AR Osteoporosis-pseudoglioma syndrome PAX2 AD Papillorenal syndrome ATOH7...

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AXIN1

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been shown to interact with: APC, CTNNB1, CSNK1E, CSNK1A1, DVL1, GSK3B, LRP5, MAP3K1, PPP2R5A, RNF43, and TSC2. GRCh38: Ensembl release 89: ENSG00000103126...

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Mesoderm development LRP chaperone

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PMID 12477932. Hsieh JC, Lee L, Zhang L, et al. (2003). "Mesd encodes an LRP5/6 chaperone essential for specification of mouse embryonic polarity". Cell...

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WNT8A

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signaling, but upon the binding of a Wnt ligand with a frizzled receptor and Lrp5/6 the 𝜷-catenin signaling molecule is no longer degraded. Instead, it interacts...

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Dishevelled

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membrane, providing a site for Axin and GSK3β to bind and phosphorylate LRP5/6 (transmembrane low-density lipoprotein receptor-related protein), preventing...

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WNT3A

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lumen extracellular region cell surface extracellular exosome Wnt-Frizzled-LRP5/6 complex early endosome membrane plasma membrane Golgi lumen presynapse...

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