Automated description from the Alliance of Genome Resources
Exhibits protease binding activity. Involved in several processes, including animal organ development; extracellular matrix organization; and skeletal system development. Localizes to the basement membrane. Used to study Schwartz-Jampel syndrome 1; Silverman-Handmaker type dyssegmental dysplasia; dextro-looped transposition of the great arteries 1; and thanatophoric dysplasia. Human ortholog(s) of this gene implicated in Schwartz-Jampel syndrome 1; Silverman-Handmaker type dyssegmental dysplasia; and osteochondrodysplasia. Orthologous to human HSPG2 (heparan sulfate proteoglycan 2).