Table 1 lists a number of putative GPCRs identified by NC-IUPHAR [191], for which preliminary evidence for an endogenous ligand has been published, or for which there exists a potential link to a disease, or disorder. These GPCRs have recently been reviewed in detail [148]. The GPCRs in Table 1 are all Class A, rhodopsin-like GPCRs. Class A orphan GPCRs not listed in Table 1 are putative GPCRs with as-yet unidentified endogenous ligands.Table 1: Class A orphan GPCRs with putative endogenous ligands GPR3GPR4GPR6GPR12GPR15GPR17GPR20 GPR22GPR26GPR31GPR34GPR35GPR37GPR39 GPR50GPR63GRP65GPR68GPR75GPR84GPR87 GPR88GPR132GPR149GPR161GPR183LGR4LGR5 LGR6MAS1MRGPRDMRGPRX1MRGPRX2P2RY10TAAR2 In addition the orphan receptors GPR18, GPR55 and...
The formylpeptide receptors (nomenclature agreed by the NC-IUPHAR Subcommittee on the formylpeptide ...
Of the druggable group of G protein-coupled receptors in the human genome, a number remain which hav...
The human gene encoding the QRFP receptor (nomenclature as agreed by the NC-IUPHAR Subcommittee on t...
Table 1 lists a number of putative GPCRs identified by NC-IUPHAR [191], for which preliminary evid...
This set contains class C 'orphan' G protein coupled receptors where the endogenous ligand(s) is not...
GPR18, GPR55 and GPR119 (provisional nomenclature), although showing little structural similarity t...
Retinoic acid receptor-related orphan receptors (ROR, nomenclature as agreed by the NC-IUPHAR Subcom...
Adhesion GPCRs are structurally identified on the basis of a large extracellular region, similar to ...
GPR3, GPR6, and GPR12 are three orphan receptors that belong to the Class A family of G-protein-coup...
n Abstract The completion of the human genome sequencing project has identified approximately 720 ge...
GPCRs are the most successful pharmaceutical targets in history. Nevertheless, the pharmacology of m...
The mammalian genome encodes seven guanylyl cyclases, GC-A to GC-G, that are homodimeric transmembra...
The mammalian genome encodes transmembrane and soluble receptor guanylyl cyclases, both of which hav...
To date, 12 members of the human ABCA subfamily are identified. They share a high degree of sequence...
grantor: University of TorontoG protein-coupled receptors (GPCRs) are integral membrane pr...
The formylpeptide receptors (nomenclature agreed by the NC-IUPHAR Subcommittee on the formylpeptide ...
Of the druggable group of G protein-coupled receptors in the human genome, a number remain which hav...
The human gene encoding the QRFP receptor (nomenclature as agreed by the NC-IUPHAR Subcommittee on t...
Table 1 lists a number of putative GPCRs identified by NC-IUPHAR [191], for which preliminary evid...
This set contains class C 'orphan' G protein coupled receptors where the endogenous ligand(s) is not...
GPR18, GPR55 and GPR119 (provisional nomenclature), although showing little structural similarity t...
Retinoic acid receptor-related orphan receptors (ROR, nomenclature as agreed by the NC-IUPHAR Subcom...
Adhesion GPCRs are structurally identified on the basis of a large extracellular region, similar to ...
GPR3, GPR6, and GPR12 are three orphan receptors that belong to the Class A family of G-protein-coup...
n Abstract The completion of the human genome sequencing project has identified approximately 720 ge...
GPCRs are the most successful pharmaceutical targets in history. Nevertheless, the pharmacology of m...
The mammalian genome encodes seven guanylyl cyclases, GC-A to GC-G, that are homodimeric transmembra...
The mammalian genome encodes transmembrane and soluble receptor guanylyl cyclases, both of which hav...
To date, 12 members of the human ABCA subfamily are identified. They share a high degree of sequence...
grantor: University of TorontoG protein-coupled receptors (GPCRs) are integral membrane pr...
The formylpeptide receptors (nomenclature agreed by the NC-IUPHAR Subcommittee on the formylpeptide ...
Of the druggable group of G protein-coupled receptors in the human genome, a number remain which hav...
The human gene encoding the QRFP receptor (nomenclature as agreed by the NC-IUPHAR Subcommittee on t...