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Description for Protein VLDLR

very low density lipoprotein receptor
8 total interacting proteins; 4 platelet interacting proteins
Icon Book Platelet Evidence (proteome studies/others : 0/0)
(Not detected in platelets)
Summary:
The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. This gene encodes a lipoprotein receptor that is a member of the LDLR family and plays important roles in VLDL-triglyceride metabolism and the reelin signaling pathway. Mutations in this gene cause VLDLR-associated cerebellar hypoplasia. Alternative splicing generates multiple transcript variants encoding distinct isoforms for this gene. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
  • SP: Signal Peptide
  • LDLA: Low-density lipoprotein receptor domain class A
  • EGFCA: Calcium-binding EGF-like domain
  • TM: Transmembrane domain
  • EGF: Epidermal growth factor-like domain.
  • EGFL: EGF domain, unclasssified subfamily

  • Gene Ontology:
    Gene Ontology Annotations

    KEGG - Enzyme ID(s):
    None Available
    KEGG - Orthology:
    None Available
    KEGG - Pathway(s):
    None Available
    Nomenclature / Alternative Names:
    Very low density lipoprotein receptor; Very low density lipoprotein receptor isoform b; Very low density lipoprotein receptor isoform a
    Approved Symbol:
    VLDLR
    (De-) Phosphorylations:
    Total (de-) phosphorylation sites: 2
    Human (de-) phosphorylation sites: 2; No platelet phosphorylation sites

    Phosphorylation Targets:
    Total phosphorylation targets: 0
    Human phosphorylation targets: 0;Predicted platelet targets: 0
    Protein Characteristics:
    Isoform-specific Information
    Icon DrugsAssociated Drugs (DrugBank Accession):

  • Lauric Acid(db)


    Associated Genetic Diseases:

  • Cerebellar hypoplasia, VLDLR-associated(Pd)
  • Predicted Transmembrane Domains:
  • Isoform 2 : 1
  • Isoform 1 : 1
  • Additional Identifiers:

    HPRD: 01895 Entrez Gene ID: 7436 OMIM ID: 192977 Swissprot Accession: P98155Q5VVF5