HAPLN1 belongs to the HAPLN family and contains 1 Ig like V type (immunoglobulin like) domain and 2 Link domains. HAPLN1 stabilizes the aggregates of proteoglycan monomers with hyaluronic acid in the extracellular cartilage matrix. Diseases associated with HAPLN1 include Cerebral Creatine Deficiency Syndrome 3 and Rheumatoid Arthritis, Systemic Juvenile.
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Protein Aliases: Cartilage link protein; cartilage linking protein 1; Cartilage-link protein; Cartilage-linking protein 1; Hyaluronan and proteoglycan link protein 1; Proteoglycan link protein
Gene Aliases: CRT1; CRTL1; HAPLN1
UniProt ID: (Human) P10915
Entrez Gene ID: (Human) 1404