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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]. |
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]