ADGRG7

gene
On this page

Also known as FLJ14454

Summary

ADGRG7 (adhesion G protein-coupled receptor G7, HGNC:19241) is a protein-coding gene on chromosome 3q12.2, encoding Adhesion G-protein coupled receptor G7 (Q96K78). Orphan receptor.

Predicted to enable G protein-coupled receptor activity. Predicted to be involved in adenylate cyclase-activating G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane.

Source: NCBI Gene 84873 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 146 total
  • MANE Select transcript: NM_032787

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:19241
Approved symbolADGRG7
Nameadhesion G protein-coupled receptor G7
Location3q12.2
Locus typegene with protein product
StatusApproved
AliasesFLJ14454
Ensembl geneENSG00000144820
Ensembl biotypeprotein_coding
OMIM612307
Entrez84873

Gene structure

Transcript identifiers

Ensembl transcripts: 6 — 3 protein_coding, 3 protein_coding_CDS_not_defined

ENST00000273352, ENST00000475887, ENST00000481361, ENST00000481506, ENST00000493081, ENST00000868805

RefSeq mRNA: 2 — MANE Select: NM_032787 NM_001308362, NM_032787

CCDS: CCDS2938, CCDS77778

Canonical transcript exons

ENST00000273352 — 16 exons

ExonStartEnd
ENSE00000967307100629598100629711
ENSE00000967309100630705100630809
ENSE00000967311100633265100633377
ENSE00000967313100635677100635826
ENSE00000967318100643526100643633
ENSE00000967320100645945100646108
ENSE00000967321100646569100646724
ENSE00000967322100649695100649807
ENSE00000967323100654835100655181
ENSE00001225265100694744100695479
ENSE00001225273100609601100609971
ENSE00003528101100659688100659843
ENSE00003570251100668949100669105
ENSE00003570753100643266100643405
ENSE00003576823100637302100637402
ENSE00003588830100655899100655995

Expression profiles

Bgee: expression breadth ubiquitous, 118 present calls, max score 94.64.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.1988 / max 105.4681, expressed in 19 samples.

FANTOM5 promoters (6 alternative TSS)

Promoter IDTPM avgSamples expressed
376230.125612
376270.02646
376260.02075
376240.00964
2028620.00863
376250.00814

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
jejunal mucosaUBERON:000039994.64gold quality
duodenumUBERON:000211490.63gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047381.63gold quality
right lobe of liverUBERON:000111480.50gold quality
small intestineUBERON:000210878.90gold quality
small intestine Peyer’s patchUBERON:000345478.89gold quality
liverUBERON:000210777.73gold quality
mucosa of transverse colonUBERON:000499175.43gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099174.03gold quality
rectumUBERON:000105271.41gold quality
jejunumUBERON:000211570.42gold quality
colonic mucosaUBERON:000031766.08gold quality
gall bladderUBERON:000211062.55gold quality
transverse colonUBERON:000115762.18gold quality
smooth muscle tissueUBERON:000113561.89gold quality
vermiform appendixUBERON:000115461.08gold quality
mucosa of sigmoid colonUBERON:000499361.06silver quality
intestineUBERON:000016060.49gold quality
caecumUBERON:000115356.51gold quality
large intestineUBERON:000005953.78gold quality
colonUBERON:000115552.80gold quality
skin of hipUBERON:000155451.28silver quality
upper leg skinUBERON:000426249.95gold quality
seminal vesicleUBERON:000099849.61gold quality
amniotic fluidUBERON:000017347.13silver quality
skeletal muscle tissue of rectus abdominisUBERON:000451143.37gold quality
secondary oocyteCL:000065542.57gold quality
mammary ductUBERON:000176542.29silver quality
endometriumUBERON:000129541.76gold quality
urinary bladderUBERON:000125541.72gold quality

Single-cell (SCXA)

Detected in 3 experiment(s), a significant marker in 3.

ExperimentMarker?Max mean expression
E-GEOD-75140yes143.27
E-GEOD-76312yes94.28
E-ANND-3yes6.23

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

37 targeting ADGRG7, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-186-5P99.9970.833707
HSA-MIR-129799.9173.413162
HSA-MIR-6809-3P99.9171.453814
HSA-MIR-5582-3P99.8672.484221
HSA-MIR-548AR-3P99.8571.263889
HSA-MIR-548AZ-3P99.8270.563549
HSA-MIR-548BC99.8270.613524
HSA-MIR-548E-3P99.8270.593514
HSA-MIR-548F-3P99.8270.593540
HSA-MIR-374C-5P99.8072.062910
HSA-MIR-655-3P99.8072.192909
HSA-MIR-26A-5P99.7873.522303
HSA-MIR-26B-5P99.7873.512305
HSA-MIR-548A-3P99.7670.583524
HSA-MIR-430699.7270.503630
HSA-MIR-446599.7172.562096
HSA-MIR-561-3P99.6470.903647
HSA-MIR-4762-5P99.5768.541424
HSA-MIR-391599.4568.491905
HSA-MIR-29799.4069.581418
HSA-MIR-185-5P99.3568.602497
HSA-MIR-464499.3569.122514
HSA-MIR-6739-3P99.2268.841843
HSA-MIR-892C-5P99.1670.562116
HSA-MIR-371A-5P99.0866.511914
HSA-MIR-607498.8969.642187
HSA-MIR-412-3P98.8666.89712
HSA-MIR-6754-3P98.8466.60889
HSA-MIR-59998.3266.991037
HSA-MIR-1212098.0568.441768

Literature-anchored findings (GeneRIF, showing 2)

  • An expressed in-frame TRK-fused gene-G-protein-coupled receptor GPR128 is identified in healthy individuals and in patients with myeloproliferative neoplasms. (PMID:19797732)
  • Upregulation of mRNA Expression of ADGRD1/GPR133 and ADGRG7/GPR128 in SARS-CoV-2-Infected Lung Adenocarcinoma Calu-3 Cells. (PMID:38786015)

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_rerioadgrg7.2ENSDARG00000071085
danio_rerioadgrg7.1ENSDARG00000071088
mus_musculusAdgrg7ENSMUSG00000022755
rattus_norvegicusAdgrg7ENSRNOG00000001634

Paralogs (42): CALCR (ENSG00000004948), GIPR (ENSG00000010310), ADGRA2 (ENSG00000020181), CALCRL (ENSG00000064989), GLP2R (ENSG00000065325), ADGRF5 (ENSG00000069122), ADGRL1 (ENSG00000072071), ADCYAP1R1 (ENSG00000078549), SCTR (ENSG00000080293), VIPR2 (ENSG00000106018), CRHR2 (ENSG00000106113), GHRHR (ENSG00000106128), ADGRD1 (ENSG00000111452), GLP1R (ENSG00000112164), ADGRG6 (ENSG00000112414), VIPR1 (ENSG00000114812), ADGRL2 (ENSG00000117114), CRHR1 (ENSG00000120088), ADGRB2 (ENSG00000121753), ADGRE5 (ENSG00000123146), ADGRE2 (ENSG00000127507), ADGRE3 (ENSG00000131355), ADGRB3 (ENSG00000135298), PTH2R (ENSG00000144407), ADGRL3 (ENSG00000150471), ADGRA3 (ENSG00000152990), ADGRF1 (ENSG00000153292), ADGRF4 (ENSG00000153294), ADGRG4 (ENSG00000156920), ADGRG5 (ENSG00000159618), PTH1R (ENSG00000160801), ADGRL4 (ENSG00000162618), EVA1C (ENSG00000166979), ADGRF3 (ENSG00000173567), ADGRG2 (ENSG00000173698), ADGRE1 (ENSG00000174837), ADGRD2 (ENSG00000180264), ADGRB1 (ENSG00000181790), ADGRG3 (ENSG00000182885), ADGRA1 (ENSG00000197177)

Protein

Protein identifiers

Adhesion G-protein coupled receptor G7Q96K78 (reviewed: Q96K78)

Alternative names: G-protein coupled receptor 128

All UniProt accessions (2): Q96K78, E9PHI0

UniProt curated annotations — full annotation on UniProt →

Function. Orphan receptor.

Subcellular location. Membrane.

Similarity. Belongs to the G-protein coupled receptor 2 family. Adhesion G-protein coupled receptor (ADGR) subfamily.

RefSeq proteins (2): NP_001295291, NP_116176* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000203GPSConserved_site
IPR000832GPCR_2_secretin-likeFamily
IPR017981GPCR_2-like_7TMDomain
IPR046338GAIN_dom_sfHomologous_superfamily
IPR047938GPR128_7tmB2Domain
IPR053066ADGR_G7Family
IPR053984GPR128_NDomain
IPR053985GPR128_GAIN_subdom_ADomain
IPR053986GPR128_GAIN_subdom_BDomain
IPR057244GAIN_BDomain

Pfam: PF00002, PF01825, PF22257, PF22259, PF22261

UniProt features (34 total): glycosylation site 10, topological domain 8, transmembrane region 7, sequence variant 3, disulfide bond 2, signal peptide 1, chain 1, domain 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q96K78-F180.480.42

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 (2): 383–410, 398–412

Glycosylation sites (10): 82, 159, 178, 191, 247, 261, 312, 316, 387, 413

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 32 (showing top): ACEVEDO_METHYLATED_IN_LIVER_CANCER_DN, GOMF_TRANSMEMBRANE_SIGNALING_RECEPTOR_ACTIVITY, GSE13522_WT_VS_IFNG_KO_SKIN_DN, chr3q12, GOMF_G_PROTEIN_COUPLED_RECEPTOR_ACTIVITY, MIKKELSEN_MEF_ICP_WITH_H3K27ME3, GOBP_G_PROTEIN_COUPLED_RECEPTOR_SIGNALING_PATHWAY, GSE13547_WT_VS_ZFX_KO_BCELL_ANTI_IGM_STIM_12H_UP, DIDO1_TARGET_GENES, ZNF2_TARGET_GENES, MIR1297, MIR12120, GSE10463_CD40L_AND_VA347_VS_CD40L_IN_DC_DN, MIR4762_5P, MIR4646_5P

GO Biological Process (3): cell surface receptor signaling pathway (GO:0007166), G protein-coupled receptor signaling pathway (GO:0007186), signal transduction (GO:0007165)

GO Molecular Function (3): G protein-coupled receptor activity (GO:0004930), transmembrane signaling receptor activity (GO:0004888), 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
signal transduction2
G protein-coupled receptor activity1
cell communication1
cellular process1
signaling1
regulation of cellular process1
cellular response to stimulus1
transmembrane signaling receptor activity1
G protein-coupled receptor signaling pathway1
signaling receptor activity1
binding1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

510 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ADGRG7ADGRA1Q86SQ6603
ADGRG7RNF25Q96BH1442
ADGRG7TMEM244Q5VVB8398
ADGRG7USF3Q68DE3375
ADGRG7NTRK1P04629370
ADGRG7CAPN12Q6ZSI9370
ADGRG7ADGRG4Q8IZF6367
ADGRG7OR51M1Q9H341354
ADGRG7ARL17BI3L3L1352
ADGRG7ARHGAP20Q9P2F6344
ADGRG7FAM221AA4D161335
ADGRG7ADGRG5Q8IZF4314
ADGRG7OR2T29Q8NH02314
ADGRG7DPYSQ14117310
ADGRG7ADGRA3Q8IWK6306

IntAct

17 interactions, top by confidence:

ABTypeScore
ADGRG7LDLRAD1psi-mi:“MI:0915”(physical association)0.780
LDLRAD1ADGRG7psi-mi:“MI:0915”(physical association)0.780
ADGRG7psi-mi:“MI:0915”(physical association)0.560
ADGRG7psi-mi:“MI:0915”(physical association)0.560
ADGRG7VAPApsi-mi:“MI:0915”(physical association)0.560
ADGRG7SORT1psi-mi:“MI:0915”(physical association)0.560
ADGRG7LDLRAD1psi-mi:“MI:0915”(physical association)0.000
ADGRG7VAPApsi-mi:“MI:0915”(physical association)0.000
ADGRG7SORT1psi-mi:“MI:0915”(physical association)0.000

BioGRID (6): GPR128 (Two-hybrid), LDLRAD1 (Two-hybrid), GPR128 (Two-hybrid), GPR128 (Two-hybrid), GPR128 (Two-hybrid), LDLRAD1 (Two-hybrid)

ESM2 similar proteins: A7E2Z9, A8K7I4, B7ZSK1, C6KFA3, P07911, P15396, P17301, P19218, P52787, P53710, Q14CN2, Q16819, Q1WIM2, Q2TU62, Q5T601, Q5VV43, Q5Y4N8, Q61549, Q62469, Q62929, Q66IR0, Q6DJ83, Q6F3F9, Q6PT52, Q6Q473, Q6QMG1, Q6YHK3, Q70VB1, Q862Z3, Q86SQ4, Q8BGZ8, Q8BLQ9, Q8BM96, Q8CJ11, Q8CJ12, Q8IZP9, Q8K4Z6, Q8N3J6, Q8TCW7, Q91X17

Diamond homologs: A6QLU6, B7ZCC9, C6KFA3, G5ECX0, O88917, O88923, O95490, O97817, O97827, O97831, P05451, P43137, P48960, Q14246, Q2Q421, Q2Q426, Q5R7Y0, Q5T601, Q5Y4N8, Q61549, Q6QNK2, Q7SY09, Q80T32, Q80TS3, Q86SQ3, Q86SQ4, Q8CJ11, Q8CJ12, Q8IZF6, Q8IZP9, Q8SQA4, Q8VEC3, Q91ZE5, Q923X1, Q96K78, Q9BY15, Q9ESC1, Q9HAR2, Q9HBW9, Q9UHX3

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance118
Likely benign12
Benign4

Top pathogenic / likely-pathogenic (0)

SpliceAI

2227 predictions. Top by Δscore:

VariantEffectΔscore
3:100629694:GAC:Gdonor_gain1.0000
3:100637296:TGGCA:Tacceptor_loss1.0000
3:100637297:GGCA:Gacceptor_loss1.0000
3:100637298:GCAG:Gacceptor_loss1.0000
3:100637299:CA:Cacceptor_loss1.0000
3:100637300:A:AGacceptor_gain1.0000
3:100637300:AGG:Aacceptor_loss1.0000
3:100637301:G:GCacceptor_gain1.0000
3:100637400:AACG:Adonor_loss1.0000
3:100637401:AC:Adonor_gain1.0000
3:100637401:ACG:Adonor_loss1.0000
3:100637402:CGT:Cdonor_loss1.0000
3:100637403:G:GCdonor_loss1.0000
3:100637403:G:GGdonor_gain1.0000
3:100637404:TAA:Tdonor_loss1.0000
3:100645940:TATA:Tacceptor_loss1.0000
3:100645941:ATAG:Aacceptor_loss1.0000
3:100645942:T:Gacceptor_gain1.0000
3:100645943:A:AGacceptor_gain1.0000
3:100645943:AGATT:Aacceptor_loss1.0000
3:100645944:G:GAacceptor_gain1.0000
3:100646107:AGGT:Adonor_loss1.0000
3:100646108:GGTG:Gdonor_loss1.0000
3:100646109:G:GGdonor_gain1.0000
3:100646109:GT:Gdonor_loss1.0000
3:100646567:A:AGacceptor_gain1.0000
3:100646568:G:GAacceptor_gain1.0000
3:100646568:GTAC:Gacceptor_gain1.0000
3:100646568:GTACA:Gacceptor_gain1.0000
3:100646601:T:Gacceptor_gain1.0000

AlphaMissense

5234 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
3:100629702:T:AC74S0.997
3:100629703:G:CC74S0.997
3:100646637:G:CW393C0.997
3:100646637:G:TW393C0.997
3:100629702:T:CC74R0.994
3:100629669:T:AC63S0.993
3:100629670:G:CC63S0.993
3:100629704:T:GC74W0.991
3:100633291:T:AC121S0.990
3:100633292:G:CC121S0.990
3:100633293:C:GC121W0.990
3:100669019:T:AW684R0.990
3:100669019:T:CW684R0.990
3:100629636:T:AC52S0.989
3:100629637:G:CC52S0.989
3:100629669:T:CC63R0.989
3:100646635:T:AW393R0.989
3:100646635:T:CW393R0.989
3:100629703:G:TC74F0.988
3:100646650:T:AC398S0.988
3:100646651:G:CC398S0.988
3:100646713:G:CA419P0.988
3:100655082:T:AW543R0.988
3:100655082:T:CW543R0.988
3:100629689:G:CW69C0.987
3:100629689:G:TW69C0.987
3:100629703:G:AC74Y0.987
3:100646616:G:CW386C0.987
3:100646616:G:TW386C0.987
3:100629675:T:AC65S0.986

dbSNP variants (sampled 300 via entrez): RS1000004829 (3:100642986 T>C), RS1000028992 (3:100692017 A>G), RS1000032965 (3:100616989 T>A,C), RS1000038121 (3:100626690 T>C), RS1000057429 (3:100670061 C>G), RS1000077932 (3:100668284 G>A), RS1000190252 (3:100653010 G>A,T), RS1000204635 (3:100614739 C>A,G), RS1000253296 (3:100624515 G>T), RS1000283046 (3:100663369 A>T), RS1000315068 (3:100620275 A>G), RS1000329827 (3:100647497 A>T), RS1000394156 (3:100674471 A>G), RS1000464792 (3:100659130 T>G), RS1000473406 (3:100615023 C>T)

Disease associations

OMIM: gene MIM:612307 | disease phenotypes: MIM:189800

GenCC curated gene-disease

Mondo (1): preeclampsia (MONDO:0005081)

Orphanet (1): Preeclampsia (Orphanet:275555)

HPO phenotypes

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

GWAS associations

1 associations (top):

StudyTraitp-value
GCST010002_434Refractive error5.000000e-25

MeSH disease descriptors (1)

DescriptorNameTree numbers
D011225Pre-EclampsiaC12.050.703.395.249

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

PharmGKB variants

1 variants.

VariantGenesLevelScore#Clin annotsDrugs
rs117308378ADGRG70.000

GtoPdb / IUPHAR curated pharmacology

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

Target class: gpcr — Adhesion Class GPCRs

CTD chemical–gene interactions

12 total (human), top 12 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyrenedecreases expression, increases methylation2
methyleugenoldecreases expression1
quercitrinincreases expression1
S-(1,2-dichlorovinyl)cysteineaffects response to substance, increases expression, affects cotreatment1
CGP 52608affects binding, increases reaction1
theaflavin-3,3’-digallateaffects expression1
Cadmiumdecreases expression1
Lipopolysaccharidesaffects response to substance, increases expression, affects cotreatment1
N-Nitrosopyrrolidinedecreases expression1
Valproic Aciddecreases methylation1
Aflatoxin B1increases methylation1
Okadaic Aciddecreases expression1

Clinical trials (associated diseases)

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

TrialPhaseStatusTitle
NCT00117546PHASE4UNKNOWNCardiovascular and Autonomic Reactivity in Women With a History of Pre-eclampsia
NCT00567957PHASE4UNKNOWNRemifentanil for General Anesthesia in Preeclamptics
NCT01030627PHASE4COMPLETEDTreatment Approaches to Preeclampsia
NCT01352234PHASE4COMPLETEDComparison of Doses of Acetylsalicylic Acid in Women With Previous History of Preeclampsia
NCT01361425PHASE4UNKNOWNAnti-Hypertensive Treatment In Stable Pregnant Women With Severe Pre-Eclampsia (Metildopape)
NCT01729468PHASE4COMPLETEDPrevention of Pre-eclampsia and SGA by Low-Dose Aspirin in Nulliparous Women With Abnormal First-trimester Uterine Artery Dopplers
NCT01761916PHASE4COMPLETEDClonidine Versus Captopril for Treatment of Postpartum Very High Blood Pressure
NCT01912677PHASE4COMPLETEDOral Antihypertensive Regimens for Management of Hypertension in Pregnancy
NCT02025426PHASE4TERMINATEDPhenylephrine Versus Ephedrine in Pre-eclampsia
NCT02091401PHASE4COMPLETEDA Trial Comparing Treatment With the Springfusor Infusion Pump to the IV Magnesium Sulfate Regimen
NCT02163655PHASE4COMPLETEDDiuretics for Postpartum High Blood Pressure in Preeclampsia
NCT02338687PHASE4COMPLETEDLow Dose Calcium to Prevent Preeclampsia
NCT02396030PHASE4TERMINATEDDifferent Schemes of Magnesium Sulfate for Preeclampsia
NCT02531490PHASE4UNKNOWNEarly Vascular Adjustments During Hypertensive Pregnancy
NCT02699827PHASE4COMPLETEDAdding MgSO4 to Epidural Levobupivacaine in CS for Patients With Preeclampsia
NCT02835339PHASE4COMPLETEDMagnesium Sulfate in Obese Preeclamptics
NCT02891174PHASE4COMPLETEDThe Effect of Ibuprofen on Post-partum Blood Pressure in Women With Hypertensive Disorders of Pregnancy
NCT02911701PHASE4COMPLETEDEffect of Acetaminophen on Postpartum Blood Pressure Control in Preeclampsia With Severe Features
NCT03171480PHASE4COMPLETEDUse of Nitrous Oxide Donor for Labor Induction in Women With PreEclampsia
NCT03233880PHASE4UNKNOWNImpact of Antichlamydial Treatment on the Rate of Preeclampsia
NCT03237000PHASE4UNKNOWNEffect of Administering Intravenous Magnesium Sulfate on Fetal Cardiotocography and Neonatal Outcome in Preeclamptic Patients
NCT03506724PHASE4COMPLETEDResponse to Anti-hypertensives in Pregnant and Postpartum Patients
NCT03674606PHASE4COMPLETEDTrial of Early Screening Test for Pre-eclampsia and Growth Restriction
NCT03735433PHASE4TERMINATEDThe Effect of Two Aspirin Dosing Strategies for Obese Women at High Risk for Preeclampsia
NCT03824119PHASE4UNKNOWNPostpartum NSAIDS and Maternal Hypertension
NCT04051567PHASE4UNKNOWNLow-dose Aspirin for Prevention of Adverse Pregnancy Outcomes in Twin Pregnancies
NCT04077853PHASE4COMPLETEDProgesterone in Expectantly Managed Early-onset Preeclampsia
NCT04158830PHASE4WITHDRAWNAspirin (ASA) Therapy and Preeclampsia Prevention
NCT04424693PHASE4UNKNOWNComparing the Incidence of Preeclampsia Between Pregnant Women Receiving Tdap Vaccinations at Week 28 or at Week 36
NCT04631627PHASE4UNKNOWNEarly Prediction and Randomised Prevention of Preeclampsia With Low Dose Aspirin in Chinese Cohort
NCT04656665PHASE4UNKNOWNThe Effectiveness of Aspirin on Preventing Pre-eclampsia
NCT04797949PHASE4WITHDRAWNAdherence to Universal Aspirin Compared to Screening Indicated Aspirin for Prevention of Preeclampsia
NCT04908982PHASE4UNKNOWNAspirin for the Prevention of Preeclampsia in Women With Stage 1 Hypertension
NCT05221164PHASE4UNKNOWN162 mg of Aspirin for Prevention of Preeclampsia
NCT05294952PHASE4UNKNOWNco Ihibtory Receptor in Preeclampsia
NCT05514847PHASE4ACTIVE_NOT_RECRUITINGLow Dose Aspirin for Preterm Preeclampsia Preventionmg/day Dose in High-risk Patients
NCT05586373PHASE4COMPLETEDIbuprofen vs Dipyrone After C-section in Preeclampsia
NCT06069102PHASE4COMPLETEDOptimal Blood Pressure Treatment Thresholds Postpartum
NCT06107335PHASE4NOT_YET_RECRUITINGEffect of Albumin Versus Routine Care on Hemodynamic Response and Stability in Patients With Preeclampsia Guided by a Non-invasive Hemodynamic Monitoring System During Cesarean Delivery With Spinal Anesthesia
NCT06281665PHASE4RECRUITINGTreatment With Aspirin After Preeclampsia: TAP Trial
  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): preeclampsia