2m96

Structural highlights

Disease

[RXFP2_HUMAN] The disease is caused by mutations affecting the gene represented in this entry.

Function

[RXFP2_HUMAN] Receptor for relaxin. The activity of this receptor is mediated by G proteins leading to stimulation of adenylate cyclase and an increase of cAMP. May also be a receptor for Leydig insulin-like peptide (INSL3).