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Gene and Protein Information ![]() |
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class A G protein-coupled receptor | ||||||
Species | TM | AA | Chromosomal Location | Gene Symbol | Gene Name | Reference |
Human | 7 | 319 | 3q25.1 | GPR171 | G protein-coupled receptor 171 | 2 |
Mouse | 7 | 319 | 3 D | Gpr171 | G protein-coupled receptor 171 | |
Rat | 7 | 326 | 2q31 | Gpr171 | G protein-coupled receptor 171 |
Previous and Unofficial Names ![]() |
G-protein coupled receptor H963 | platelet activating receptor homolog |
Database Links ![]() |
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Specialist databases | |
GPCRdb | gp171_human (Hs) |
Other databases | |
Alphafold | O14626 (Hs), Q8BG55 (Mm) |
ChEMBL Target | CHEMBL4523860 (Hs) |
Ensembl Gene | ENSG00000174946 (Hs), ENSMUSG00000050075 (Mm), ENSRNOG00000025297 (Rn) |
Entrez Gene | 29909 (Hs), 229323 (Mm), 688737 (Rn) |
Human Protein Atlas | ENSG00000174946 (Hs) |
KEGG Gene | hsa:29909 (Hs), mmu:229323 (Mm), rno:688737 (Rn) |
Pharos | O14626 (Hs) |
RefSeq Nucleotide | NM_013308 (Hs), NM_173398 (Mm), NM_001109510 (Rn) |
RefSeq Protein | NP_013308 (Hs), NP_775574 (Mm), NP_001102980 (Rn) |
UniProtKB | O14626 (Hs), Q8BG55 (Mm) |
Wikipedia | GPR171 (Hs) |
Agonist Comments | ||
GPR171 has been shown to be activated by endogenous peptide BigLEN. This receptor-peptide interaction is believed to be involved in regulating feeding and metabolism responses [1]. |
Immuno Process Associations | ||||||||||||
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Expression Datasets ![]() |
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Biologically Significant Variants ![]() |
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General Comments |
GPR171 is excluded as a candidate gene of Usher syndrome Type 3 [3]. |
1. Gomes I, Aryal DK, Wardman JH, Gupta A, Gagnidze K, Rodriguiz RM, Kumar S, Wetsel WC, Pintar JE, Fricker LD et al.. (2013) GPR171 is a hypothalamic G protein-coupled receptor for BigLEN, a neuropeptide involved in feeding. Proc Natl Acad Sci USA, 110 (40): 16211-6. [PMID:24043826]
2. Jacobs KA, Collins-Racie LA, Colbert M, Duckett M, Golden-Fleet M, Kelleher K, Kriz R, LaVallie ER, Merberg D, Spaulding V et al.. (1997) A genetic selection for isolating cDNAs encoding secreted proteins. Gene, 198 (1-2): 289-96. [PMID:9370294]
3. Joensuu T, Hämäläinen R, Yuan B, Johnson C, Tegelberg S, Gasparini P, Zelante L, Pirvola U, Pakarinen L, Lehesjoki AE et al.. (2001) Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3. Am J Hum Genet, 69 (4): 673-84. [PMID:11524702]