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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 | 375 | 3p13 | GPR27 | G protein-coupled receptor 27 | 3-4 |
Mouse | 7 | 379 | 6 D3 | Gpr27 | G protein-coupled receptor 27 | |
Rat | 7 | 377 | 4q34 | Gpr27 | G protein-coupled receptor 27 |
Previous and Unofficial Names ![]() |
super conserved receptor expressed in brain 1 | SREB1 |
Database Links ![]() |
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Specialist databases | |
GPCRdb | gpr27_human (Hs), gpr27_mouse (Mm), gpr27_rat (Rn) |
Other databases | |
Alphafold | Q9NS67 (Hs), O54897 (Mm), Q9JJH3 (Rn) |
ChEMBL Target | CHEMBL4523923 (Hs) |
Ensembl Gene | ENSG00000170837 (Hs), ENSMUSG00000072875 (Mm), ENSRNOG00000010880 (Rn) |
Entrez Gene | 2850 (Hs), 14761 (Mm), 65275 (Rn) |
Human Protein Atlas | ENSG00000170837 (Hs) |
KEGG Gene | hsa:2850 (Hs), mmu:14761 (Mm), rno:65275 (Rn) |
OMIM | 605187 (Hs) |
Pharos | Q9NS67 (Hs) |
RefSeq Nucleotide | NM_018971 (Hs), NM_008158 (Mm), NM_023099 (Rn) |
RefSeq Protein | NP_061844 (Hs), NP_032184 (Mm), NP_075587 (Rn) |
UniProtKB | Q9NS67 (Hs), O54897 (Mm), Q9JJH3 (Rn) |
Wikipedia | GPR27 (Hs) |
Primary Transduction Mechanisms ![]() |
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Transducer | Effector/Response |
Gq/G11 family | Phospholipase C stimulation |
Comments: Alteration of gene expression affects stimulation of IP3 [1] | |
References: |
Tissue Distribution ![]() |
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Tissue Distribution Comments | ||||||||
GPR27 has been detected at higher levels in fetal brains than in adult brains, suggesting a role in neural plasticity. The receptor is highly conserved amongst mammals, with expression seen in grey matter areas of the monkey brain (hippocampal dentate gyrus and supraoptic nucleus of the hypothalamus) as demonstrated by in situ hybridisation [2]. |
Expression Datasets ![]() |
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Physiological Consequences of Altering Gene Expression ![]() |
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Clinically-Relevant Mutations and Pathophysiology Comments |
GPR27 mapped to a 15Mb constitutional de novo interstitial deletion of chromosome 3 shown to cause developmental delay and congenital anomalies. Deletion is also seen along with FOXP1, EIF4E3 and PROK2 resulting in speech delay, contractures, hypertonia and blepharophimosis, although the physiological role (if any) of GPR27 is unknown [5-6]. |
1. Ku GM, Pappalardo Z, Luo CC, German MS, McManus MT. (2012) An siRNA screen in pancreatic beta cells reveals a role for Gpr27 in insulin production. PLoS Genet, 8 (1): e1002449. [PMID:22253604]
2. Matsumoto M, Beltaifa S, Weickert CS, Herman MM, Hyde TM, Saunders RC, Lipska BK, Weinberger DR, Kleinman JE. (2005) A conserved mRNA expression profile of SREB2 (GPR85) in adult human, monkey, and rat forebrain. Brain Res Mol Brain Res, 138 (1): 58-69. [PMID:15893849]
3. Matsumoto M, Saito T, Takasaki J, Kamohara M, Sugimoto T, Kobayashi M, Tadokoro M, Matsumoto S, Ohishi T, Furuichi K. (2000) An evolutionarily conserved G-protein coupled receptor family, SREB, expressed in the central nervous system. Biochem Biophys Res Commun, 272 (2): 576-82. [PMID:10833454]
4. O'Dowd BF, Nguyen T, Marchese A, Cheng R, Lynch KR, Heng HH, Kolakowski Jr LF, George SR. (1998) Discovery of three novel G-protein-coupled receptor genes. Genomics, 47 (2): 310-3. [PMID:9479505]
5. Pariani MJ, Spencer A, Graham JM, Rimoin DL. (2009) A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis. Eur J Med Genet, 52 (2-3): 123-7. [PMID:19332160]
6. Petek E, Windpassinger C, Simma B, Mueller T, Wagner K, Kroisel PM. (2003) Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomalies. J Hum Genet, 48 (6): 283-7. [PMID:12836054]