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Target id: 145
Nomenclature: GPR174
Family: Class A Orphans with emerging pharmacology
This receptor has a proposed ligand; see the Latest Pairings page for more information.
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 | 333 | Xq21.1 | GPR174 | G protein-coupled receptor 174 | |
Mouse | 7 | 335 | X D | Gpr174 | G protein-coupled receptor 174 | |
Rat | 7 | 335 | Xq31 | Gpr174 | G protein-coupled receptor 174 |
Previous and Unofficial Names ![]() |
FKSG79 |
Database Links ![]() |
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Specialist databases | |
GPCRdb | gp174_human (Hs), gp174_mouse (Mm) |
Other databases | |
Alphafold | Q9BXC1 (Hs), Q3U507 (Mm) |
ChEMBL Target | CHEMBL3562167 (Hs), CHEMBL3813587 (Mm) |
Ensembl Gene | ENSG00000147138 (Hs), ENSMUSG00000073008 (Mm), ENSRNOG00000032970 (Rn) |
Entrez Gene | 84636 (Hs), 213439 (Mm), 302373 (Rn) |
Human Protein Atlas | ENSG00000147138 (Hs) |
KEGG Gene | hsa:84636 (Hs), mmu:213439 (Mm), rno:302373 (Rn) |
OMIM | 300903 (Hs) |
Pharos | Q9BXC1 (Hs) |
RefSeq Nucleotide | NM_032553 (Hs), NM_001033251 (Mm), NM_001106938 (Rn) |
RefSeq Protein | NP_115942 (Hs), NP_001028423 (Mm), NP_001100408 (Rn) |
UniProtKB | Q9BXC1 (Hs), Q3U507 (Mm) |
Wikipedia | GPR174 (Hs) |
Natural/Endogenous Ligands ![]() |
lysophosphatidylserine |
Comments: Proposed ligand, two publications |
Download all structure-activity data for this target as a CSV file
Agonists | |||||||||||||||||||||||||||||||||||||||||||||||||||
Key to terms and symbols | View all chemical structures | Click column headers to sort | |||||||||||||||||||||||||||||||||||||||||||||||||
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Agonist Comments | |||||||||||||||||||||||||||||||||||||||||||||||||||
GPR174 has been shown to be activated by lysophosphatidylserine, with coupling to cAMP and ERK [2,4]. |
Immuno Process Associations | ||||||||||||
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Expression Datasets ![]() |
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Clinically-Relevant Mutations and Pathophysiology ![]() |
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Gene Expression and Pathophysiology Comments | |
GPR174 was found to be overexpressed in subcutaneous melanomametastases [3]. |
Biologically Significant Variants ![]() |
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Biologically Significant Variant Comments | ||||||||||||||||||||||
A number of rare single nucleotide polymorphisms are reported by Chu et al. in their genome-wide assocation study as being associated with Graves' disease. However, with the exception of rs3827440, none of these variants occured at a frequency of more than 5% in the population studied [1]. |
1. Chu X, Shen M, Xie F, Miao XJ, Shou WH, Liu L, Yang PP, Bai YN, Zhang KY, Yang L et al.. (2013) An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease. J Med Genet, 50 (7): 479-85. [PMID:23667180]
2. Inoue A, Ishiguro J, Kitamura H, Arima N, Okutani M, Shuto A, Higashiyama S, Ohwada T, Arai H, Makide K et al.. (2012) TGFα shedding assay: an accurate and versatile method for detecting GPCR activation. Nat Methods, 9 (10): 1021-9. [PMID:22983457]
3. Qin Y, Verdegaal EM, Siderius M, Bebelman JP, Smit MJ, Leurs R, Willemze R, Tensen CP, Osanto S. (2011) Quantitative expression profiling of G-protein-coupled receptors (GPCRs) in metastatic melanoma: the constitutively active orphan GPCR GPR18 as novel drug target. Pigment Cell Melanoma Res, 24 (1): 207-18. [PMID:20880198]
4. Sugita K, Yamamura C, Tabata K, Fujita N. (2013) Expression of orphan G-protein coupled receptor GPR174 in CHO cells induced morphological changes and proliferation delay via increasing intracellular cAMP. Biochem Biophys Res Commun, 430 (1): 190-5. [PMID:23178570]
5. Zhao SX, Xue LQ, Liu W, Gu ZH, Pan CM, Yang SY, Zhan M, Wang HN, Liang J, Gao GQ et al.. (2013) Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. Hum Mol Genet, 22 (16): 3347-62. [PMID:23612905]