GPR152

gene
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Also known as PGR5

Summary

GPR152 (G protein-coupled receptor 152, HGNC:23622) is a protein-coding gene on chromosome 11q13.2, encoding Probable G-protein coupled receptor 152 (Q8TDT2). Orphan receptor.

Enables identical protein binding activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane.

Source: NCBI Gene 390212 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 61 total
  • Druggable target: yes
  • MANE Select transcript: NM_206997

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:23622
Approved symbolGPR152
NameG protein-coupled receptor 152
Location11q13.2
Locus typegene with protein product
StatusApproved
AliasesPGR5
Ensembl geneENSG00000175514
Ensembl biotypeprotein_coding
Entrez390212

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000312457

RefSeq mRNA: 1 — MANE Select: NM_206997 NM_206997

CCDS: CCDS8165

Canonical transcript exons

ENST00000312457 — 1 exons

ExonStartEnd
ENSE000011859726745130167452729

Expression profiles

Bgee: expression breadth tissue_specific, 8 present calls, max score 59.83.

Top tissues by expression

121 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
bone marrow cellCL:000209259.83gold quality
granulocyteCL:000009455.98gold quality
bone marrowUBERON:000237147.61gold quality
colonic epitheliumUBERON:000039746.34gold quality
sural nerveUBERON:001548844.03gold quality
spleenUBERON:000210639.54silver quality
tonsilUBERON:000237239.11gold quality
skeletal muscle tissueUBERON:000113438.05gold quality
ventricular zoneUBERON:000305336.48gold quality
mucosa of transverse colonUBERON:000499136.48gold quality
cortical plateUBERON:000534336.47gold quality
lymph nodeUBERON:000002936.45gold quality
monocyteCL:000057635.82gold quality
hindlimb stylopod muscleUBERON:000425235.65gold quality
mucosa of stomachUBERON:000119935.60silver quality
small intestine Peyer’s patchUBERON:000345435.60gold quality
ganglionic eminenceUBERON:000402335.49gold quality
vermiform appendixUBERON:000115435.36gold quality
small intestineUBERON:000210835.28gold quality
muscle tissueUBERON:000238534.50gold quality
liverUBERON:000210731.91gold quality
body of stomachUBERON:000116130.29silver quality
stomachUBERON:000094530.24silver quality
lungUBERON:000204829.96gold quality
stromal cell of endometriumCL:000225529.87gold quality
placentaUBERON:000198729.61gold quality
right uterine tubeUBERON:000130229.12gold quality
uterine cervixUBERON:000000228.99gold quality
olfactory segment of nasal mucosaUBERON:000538628.88gold quality
upper lobe of left lungUBERON:000895228.67gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.32

Regulation

Is transcription factor: no

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusGpr152ENSMUSG00000044724
rattus_norvegicusGpr152ENSRNOG00000021912

Paralogs (10): MAS1 (ENSG00000130368), MRGPRX1 (ENSG00000170255), MRGPRF (ENSG00000172935), MRGPRD (ENSG00000172938), MRGPRX4 (ENSG00000179817), MRGPRX3 (ENSG00000179826), MRGPRG (ENSG00000182170), MRGPRX2 (ENSG00000183695), MRGPRE (ENSG00000184350), MAS1L (ENSG00000204687)

Protein

Protein identifiers

Probable G-protein coupled receptor 152Q8TDT2 (reviewed: Q8TDT2)

Alternative names: G-protein coupled receptor PGR5

All UniProt accessions (2): Q8TDT2, A0A0I9RJ67

UniProt curated annotations — full annotation on UniProt →

Function. Orphan receptor.

Subcellular location. Cell membrane.

Similarity. Belongs to the G-protein coupled receptor 1 family.

RefSeq proteins (1): NP_996880* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR017452GPCR_Rhodpsn_7TMDomain
IPR026234MRGPCRFAMILYFamily

Pfam: PF00001

UniProt features (23 total): topological domain 8, transmembrane region 7, compositionally biased region 3, region of interest 2, chain 1, disulfide bond 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8TDT2-F171.720.36

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Disulfide bonds (1): 104–182

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 23 (showing top): chr11q13, NIKOLSKY_BREAST_CANCER_11Q12_Q14_AMPLICON, GOMF_TRANSMEMBRANE_SIGNALING_RECEPTOR_ACTIVITY, GOMF_G_PROTEIN_COUPLED_RECEPTOR_ACTIVITY, MARTENS_TRETINOIN_RESPONSE_DN, GOBP_G_PROTEIN_COUPLED_RECEPTOR_SIGNALING_PATHWAY, WAKABAYASHI_ADIPOGENESIS_PPARG_RXRA_BOUND_8D, RAO_BOUND_BY_SALL4_ISOFORM_B, GSE11924_TH2_VS_TH17_CD4_TCELL_DN, ZBED5_TARGET_GENES, ZAK_PBMC_MRKAD5_HIV_1_GAG_POL_NEF_AGE_20_50YO_CORRELATED_WITH_CD8_T_CELL_RESPONSE_3DY_NEGATIVE, GSE20366_CD103_KLRG1_DP_VS_DN_TREG_UP, GOMF_MOLECULAR_TRANSDUCER_ACTIVITY, GSE369_PRE_VS_POST_IL6_INJECTION_IFNG_WT_LIVER_UP, GSE8921_3H_VS_24H_TLR1_2_STIM_MONOCYTE_DN

GO Biological Process (2): G protein-coupled receptor signaling pathway (GO:0007186), signal transduction (GO:0007165)

GO Molecular Function (3): G protein-coupled receptor activity (GO:0004930), identical protein binding (GO:0042802), protein binding (GO:0005515)

GO Cellular Component (2): plasma membrane (GO:0005886), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
G protein-coupled receptor activity1
signal transduction1
cell communication1
cellular process1
signaling1
regulation of cellular process1
cellular response to stimulus1
transmembrane signaling receptor activity1
G protein-coupled receptor signaling pathway1
protein binding1
binding1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

666 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
GPR152GLIS3Q8NEA6791
GPR152GPR108Q9NPR9632
GPR152GPR171O14626578
GPR152GPR158Q5T848525
GPR152PPP1R26Q5T8A7524
GPR152GPR148Q8TDV2514
GPR152GPHRAB7ZAQ6508
GPR152GPR162Q16538507
GPR152PTRH1Q86Y79498
GPR152GPR82Q96P67490
GPR152GPR139Q6DWJ6480
GPR152TMEM134Q9H6X4477
GPR152CABP4P57796456
GPR152TOR2AQ5JU69454
GPR152GPR137Q96N19446

IntAct

577 interactions, top by confidence:

ABTypeScore
TMPPEGPR152psi-mi:“MI:0915”(physical association)0.560
ABCG4GPR152psi-mi:“MI:0915”(physical association)0.560
GPR152SLC13A4psi-mi:“MI:0915”(physical association)0.000
GPR152CLN5psi-mi:“MI:0915”(physical association)0.000
VAMP4GPR152psi-mi:“MI:0915”(physical association)0.000
MGLLGPR152psi-mi:“MI:0915”(physical association)0.000
MMDGPR152psi-mi:“MI:0915”(physical association)0.000
TMEM208GPR152psi-mi:“MI:0915”(physical association)0.000
EDDM3BGPR152psi-mi:“MI:0915”(physical association)0.000
PIGFGPR152psi-mi:“MI:0915”(physical association)0.000
TMEM97GPR152psi-mi:“MI:0915”(physical association)0.000
TIMMDC1GPR152psi-mi:“MI:0915”(physical association)0.000
TMEM243GPR152psi-mi:“MI:0915”(physical association)0.000
INSIG2GPR152psi-mi:“MI:0915”(physical association)0.000
TMEM50BGPR152psi-mi:“MI:0915”(physical association)0.000
SYT15GPR152psi-mi:“MI:0915”(physical association)0.000
SACM1LGPR152psi-mi:“MI:0915”(physical association)0.000
CYB561A3GPR152psi-mi:“MI:0915”(physical association)0.000
GPR152ABHD16Apsi-mi:“MI:0915”(physical association)0.000
RABAC1GPR152psi-mi:“MI:0915”(physical association)0.000
LHFPL2GPR152psi-mi:“MI:0915”(physical association)0.000
CLEC17AGPR152psi-mi:“MI:0915”(physical association)0.000
IGF2GPR152psi-mi:“MI:0915”(physical association)0.000
BNIP2GPR152psi-mi:“MI:0915”(physical association)0.000
SMCO4GPR152psi-mi:“MI:0915”(physical association)0.000
YIPF1GPR152psi-mi:“MI:0915”(physical association)0.000
GJB2GPR152psi-mi:“MI:0915”(physical association)0.000
CCDC167GPR152psi-mi:“MI:0915”(physical association)0.000
PTPRNGPR152psi-mi:“MI:0915”(physical association)0.000
LTC4SGPR152psi-mi:“MI:0915”(physical association)0.000

BioGRID (199): GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid), GPR152 (Two-hybrid)

ESM2 similar proteins: A0A0R4IP11, O00421, O14931, O15218, O15533, O35457, O60883, O88186, P33076, P61484, P79621, Q16570, Q16671, Q17QD8, Q3U3F9, Q5BK54, Q5TJE4, Q61790, Q6PZD2, Q7TQP4, Q7TSN6, Q7Z7M1, Q80SS6, Q80T02, Q863H8, Q8BL07, Q8BXQ3, Q8BXS7, Q8IZF5, Q8K1T1, Q8MII8, Q8MJ02, Q8N386, Q8TDT2, Q8TDU6, Q8TDV2, Q95LF2, Q95LF3, Q95LF4, Q95LF5

Diamond homologs: A0A4W3GG95, A0A6I8PUB9, B2GV46, B5X337, D4A7K7, E7FEL0, E9QJ73, F8VQN3, O00270, O08726, O08858, O14842, O14843, O15529, O42179, O43603, O46685, O60755, O77408, O88410, O88626, O88634, O88853, P21109, P23944, P25024, P25025, P35344, P35383, P35414, P41231, P41232, P46092, P46093, P49652, P49682, P49683, P50132, P51675, P51679

SIGNOR signaling

0 interactions.

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 157 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

GO biological processes:

GO termPartnersFoldFDR
vesicle fusion522.5×2e-03
cholesterol biosynthetic process515.7×6e-03

Disease & clinical

Clinical variants and AI predictions

ClinVar

61 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance51
Likely benign10
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

60 predictions. Top by Δscore:

VariantEffectΔscore
11:67451834:C:CTacceptor_gain0.5000
11:67452135:T:TAdonor_gain0.5000
11:67452142:T:TAdonor_gain0.4500
11:67451829:C:CCacceptor_gain0.4100
11:67451902:C:CAdonor_gain0.4000
11:67452636:C:CTdonor_gain0.3900
11:67451828:A:ACacceptor_gain0.3700
11:67451642:GTTCA:Gdonor_loss0.3600
11:67451643:TTCA:Tdonor_loss0.3600
11:67451644:TCACC:Tdonor_loss0.3600
11:67451645:CAC:Cdonor_loss0.3600
11:67451646:A:Tdonor_loss0.3600
11:67451647:C:Adonor_loss0.3600
11:67451648:C:Adonor_loss0.3600
11:67451928:T:TAdonor_gain0.3600
11:67451929:C:Adonor_gain0.3600
11:67452213:T:TGacceptor_gain0.3600
11:67451649:T:Cdonor_loss0.3500
11:67451650:GAGGC:Gacceptor_gain0.3500
11:67451835:A:Cacceptor_gain0.3500
11:67452637:C:CTdonor_gain0.3500
11:67451901:T:TAdonor_gain0.3400
11:67452214:C:Aacceptor_gain0.3400
11:67451610:G:Cdonor_gain0.3300
11:67451641:GGTTC:Gdonor_loss0.3300
11:67452197:C:CTdonor_gain0.3300
11:67451599:G:Cdonor_gain0.3100
11:67451832:GCCA:Gacceptor_gain0.3000
11:67451834:C:Tacceptor_gain0.3000
11:67451832:G:Adonor_gain0.2900

AlphaMissense

2982 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
11:67452434:C:AW97C0.995
11:67452434:C:GW97C0.995
11:67452509:G:CS72R0.992
11:67452509:G:TS72R0.992
11:67452511:T:GS72R0.992
11:67452236:G:CS163R0.990
11:67452236:G:TS163R0.990
11:67452238:T:GS163R0.990
11:67452347:G:CS126R0.989
11:67452347:G:TS126R0.989
11:67452349:T:GS126R0.989
11:67452414:C:TC104Y0.987
11:67452179:G:CC182W0.985
11:67452180:C:TC182Y0.985
11:67452436:A:GW97R0.985
11:67452436:A:TW97R0.985
11:67452413:G:CC104W0.983
11:67452414:C:GC104S0.983
11:67452415:A:TC104S0.983
11:67452180:C:GC182S0.982
11:67452181:A:TC182S0.982
11:67452181:A:GC182R0.981
11:67452598:C:GG43R0.981
11:67452598:C:TG43R0.981
11:67452259:A:GW156R0.978
11:67452259:A:TW156R0.978
11:67451861:G:CS288R0.977
11:67451861:G:TS288R0.977
11:67451863:T:GS288R0.977
11:67452415:A:GC104R0.976

dbSNP variants (sampled 300 via entrez): RS1000829672 (11:67453427 C>A), RS1002268917 (11:67452439 G>A,C), RS1002333604 (11:67450885 G>A,C), RS1003199431 (11:67454310 C>T), RS1003504971 (11:67452192 T>C), RS1003935148 (11:67451335 C>A,T), RS1006422325 (11:67450908 C>T), RS1008631970 (11:67453682 T>A,G), RS1011028115 (11:67451064 CTGTG>C,CTG), RS1011176578 (11:67452944 C>G,T), RS1013205351 (11:67450850 G>A), RS1013487922 (11:67452393 C>T), RS1014073489 (11:67454505 G>A), RS1014542338 (11:67454293 G>A,C), RS1015129780 (11:67451159 C>T)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

2 associations (top):

StudyTraitp-value
GCST003810_1Non-response to citalopram or escitalopram and depression1.000000e-06
GCST010002_241Refractive error3.000000e-13

Drugs & pharmacology

Drug and pharmacology data

Is drug target: yes

ChEMBL targets (1): CHEMBL4523900 (SINGLE PROTEIN)

PharmGKB: 1 entry (VIP=true, CPIC=false)

GtoPdb / IUPHAR curated pharmacology

(IUPHAR/BPS Guide to Pharmacology — expert-curated)

Target class: gpcr — Class A Orphans with no pharmacology

CTD chemical–gene interactions

4 total (human), top 4 by PubMed support.

ChemicalActions (top 5)PubMed papers
Resveratrolaffects cotreatment, decreases expression1
Benzo(a)pyreneaffects methylation, increases methylation1
Plant Extractsaffects cotreatment, decreases expression1
Valproic Acidincreases methylation1

ChEMBL screening assays

2 unique, capped per target: 2 binding

Representative assays (with source publication via chembl_document):

Assay IDTypeDescriptionSource paper
CHEMBL4883421BindingPRESTO-Tango GPCRome screening (GPR152)Data for DCP probe UCSF924

Cellosaurus cell lines

2 cell lines: 1 spontaneously immortalized cell line, 1 transformed cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_KX42PathHunter CHO-K1 GPR152 beta-arrestinSpontaneously immortalized cell lineFemale
CVCL_KZ53PathHunter HEK 293 GPR152 beta-arrestinTransformed cell lineFemale

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): mood disorder