1. Gene
  2. GPR151 - G protein-coupled receptor 151 Gene

GPR151 - G protein-coupled receptor 151 Gene

Homo sapiens

Also known as GPCR; PGR7; GALR4; GALRL; GPCR-2037

Gene ID: 134391 | Gene type: protein coding

About GPR151

Cytogenetic location: 5q32 Genomic coordinates (GRCh38): 5:146,513,144-146,516,190 (from NCBI)

This gene has 1 transcript (splice variant), 176 orthologues and 7 paralogues.

Summary

This gene encodes an orphan member of the class A rhodopsin-like family of G-protein-coupled receptors (GPCRs). Within the rhodopsin-like family, this gene is a member of the SOG subfamily that includes somatostatin, opioid, Galanin, and kisspeptin receptors. The orthologous mouse gene has a restricted pattern of neuronal expression which is induced following nerve injury. All GPCRs have a transmembrane domain that includes seven transmembrane alpha-helices. A general feature of GPCR signaling is the agonist-induced conformational change in the receptor, leading to activation of the heterotrimeric G protein. The activated G protein then binds to and activates numerous downstream effector proteins, which generate second messengers that mediate a broad range of cellular and physiological processes. [provided by RefSeq, Jul 2017]

GPR151 Products(1)

mRNA Protein Name
NM_194251.3 NP_919227.2 G-protein coupled receptor 151
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables G protein-coupled receptor activity IMP
IMP: Inferred from mutant phenotype
31119277 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Biological Process GO Annotation Evidence Reference Source
involved in G protein-coupled receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
31119277 GOA
involved in response to acidic pH IMP
IMP: Inferred from mutant phenotype
31119277 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

GPR151 Protein Structure

7tm_1

7tm_1: 7 transmembrane receptor (rhodopsin family) (53 - 306)

  • 0
  • 100
  • 200
  • 300
  • 419 a.a.
Protein Preferred Names Protein Names

G-protein coupled receptor 151

G-protein coupled receptor PGR7

GPR151 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
GPR151 Q8TDV0 SLC41A2 Homo sapiens Q96JW4 32296183
Intra
GPR151 Q8TDV0 PGRMC2 Homo sapiens O15173 32296183
Intra
GPR151 Q8TDV0 PGRMC2 Homo sapiens O15173 32296183
Intra
GPR151 Q8TDV0 TMEM239 Homo sapiens Q8WW34-2 32296183
Intra
GPR151 Q8TDV0 GPX8 Homo sapiens Q8TED1 32296183
Intra
GPR151 Q8TDV0 GPX8 Homo sapiens Q8TED1 32296183
Intra
GPR151 Q8TDV0 GPX8 Homo sapiens Q8TED1 32296183
Intra
GPR151 Q8TDV0 TMEM179B Homo sapiens Q7Z7N9 32296183
Intra
GPR151 Q8TDV0 TMEM179B Homo sapiens Q7Z7N9 32296183
Intra
GPR151 Q8TDV0 AQP6 Homo sapiens Q13520 32296183
Intra
GPR151 Q8TDV0 AQP6 Homo sapiens Q13520 32296183
Intra
GPR151 Q8TDV0 GPR152 Homo sapiens Q8TDT2 32296183
Intra
GPR151 Q8TDV0 GPR152 Homo sapiens Q8TDT2 32296183
Intra
GPR151 Q8TDV0 UNC93A Homo sapiens Q86WB7-2 32296183
Intra
GPR151 Q8TDV0 UNC93A Homo sapiens Q86WB7-2 32296183
Intra
GPR151 Q8TDV0 SCN3B Homo sapiens Q9NY72 32296183
Intra
GPR151 Q8TDV0 SCN3B Homo sapiens Q9NY72 32296183
Intra
GPR151 Q8TDV0 SCN3B Homo sapiens Q9NY72 32296183
Intra
GPR151 Q8TDV0 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
GPR151 Q8TDV0 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
GPR151 Q8TDV0 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
GPR151 Q8TDV0 GJA8 Homo sapiens P48165 32296183
Intra
GPR151 Q8TDV0 GJA8 Homo sapiens P48165 32296183
Intra
GPR151 Q8TDV0 SLC18A1 Homo sapiens P54219-3 32296183
Intra
GPR151 Q8TDV0 SLC18A1 Homo sapiens P54219-3 32296183
Intra
GPR151 Q8TDV0 SLC18A2 Homo sapiens Q05940 32296183
Intra
GPR151 Q8TDV0 SLC18A2 Homo sapiens Q05940 32296183
Intra
GPR151 Q8TDV0 SHISAL1 Homo sapiens Q3SXP7 32296183
Intra
GPR151 Q8TDV0 SHISAL1 Homo sapiens Q3SXP7 32296183
Intra
GPR151 Q8TDV0 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
GPR151 Q8TDV0 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
GPR151 Q8TDV0 FAM209A Homo sapiens Q5JX71 32296183
Intra
GPR151 Q8TDV0 FAM209A Homo sapiens Q5JX71 32296183
Intra
GPR151 Q8TDV0 CGRRF1 Homo sapiens Q99675 32296183
Intra
GPR151 Q8TDV0 CGRRF1 Homo sapiens Q99675 32296183
Intra
GPR151 Q8TDV0 CGRRF1 Homo sapiens Q99675 32296183
Intra
GPR151 Q8TDV0 CERS4 Homo sapiens Q9HA82 32296183
Intra
GPR151 Q8TDV0 CERS4 Homo sapiens Q9HA82 32296183
Intra
GPR151 Q8TDV0 CERS4 Homo sapiens Q9HA82 32296183
Intra
GPR151 Q8TDV0 CYBC1 Homo sapiens Q9BQA9 32296183
Intra
GPR151 Q8TDV0 MANBAL Homo sapiens Q9NQG1 32296183
Intra
GPR151 Q8TDV0 MANBAL Homo sapiens Q9NQG1 32296183
Intra
GPR151 Q8TDV0 MANBAL Homo sapiens Q9NQG1 32296183
Intra
GPR151 Q8TDV0 SACM1L Homo sapiens Q9NTJ5 32296183
Intra
GPR151 Q8TDV0 SLC10A1 Homo sapiens Q14973 32296183
Intra
GPR151 Q8TDV0 SLC10A1 Homo sapiens Q14973 32296183
Intra
GPR151 Q8TDV0 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
GPR151 Q8TDV0 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
GPR151 Q8TDV0 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
GPR151 Q8TDV0 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
GPR151 Q8TDV0 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
GPR151 Q8TDV0 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
GPR151 Q8TDV0 BCL2L2 Homo sapiens Q92843 32296183
Intra
GPR151 Q8TDV0 STX8 Homo sapiens Q9UNK0 32296183
Intra
GPR151 Q8TDV0 KEAP1 Homo sapiens Q14145 32296183
Intra
GPR151 Q8TDV0 KEAP1 Homo sapiens Q14145 32296183
Intra
GPR151 Q8TDV0 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
GPR151 Q8TDV0 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
GPR151 Q8TDV0 ERGIC3 Homo sapiens Q9Y282 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Essential Tremor

Benign Essential Tremor

Familial Tremor

Hereditary Essential Tremor

Essential Hereditary Tremor

Shaky Hand Syndrome

Benign Essential Tremor Syndrome

Tremor Hereditary Essential

Essential Tremor, Susceptibility To

Tremor, Hereditary Essential

Tremor, Hereditary Essential, 4

ETM4

Essential Tremor 4

Essential Tremor, Hereditary, 4

Hereditary Essential Tremor 4

Tremor, Hereditary Essential 4

Tremor, Hereditary Essential, Type 4

Brachial Plexus Lesion

Brachial Plexus Injuries

Brachial Plexus Lesions

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus GPR151 VGNC VGNC:29558
Canis familiaris GPR151 VGNC VGNC:41405
Mus musculus GPR151 MGD MGI:2441887
Rattus norvegicus GPR151 RGD RGD:727873
Felis catus GPR151 VGNC VGNC:62679
Macaca mulatta GPR151 VGNC VGNC:72987