Gastritis

disease
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Also known as acute gastric mucosal erosionerosive gastritiserosive gastropathygastritis (disease)inflammation of stomachstomach inflammation

Summary

Gastritis (MONDO:0004966) is a disease (an umbrella term covering 16 Mondo subtypes) with 4 cohort genes (21 GWAS associations across 42 studies) and 86 clinical trials. Top therapeutic interventions include amoxicillin, berberine, and clarithromycin.

At a glance

  • Umbrella term: 16 Mondo subtypes
  • Cohort genes: 4
  • GWAS associations: 21
  • Clinical trials: 86

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namegastritis
Mondo IDMONDO:0004966
EFOEFO:0000217
MeSHD005756
DOIDDOID:4029
ICD-111871672644
NCITC26780
SNOMED CT4556007
UMLSC0017152
MedGen4843
Is cancer (heuristic)no

Also known as: acute gastric mucosal erosion · erosive gastritis · erosive gastropathy · gastritis · gastritis (disease) · inflammation of stomach · stomach inflammation

Data availability: 21 GWAS associations (42 studies) · 1 HPO phenotype · 1 cell line.

Disease family

An umbrella term covering 16 Mondo subtypes.

Classification path: disease › human disease › disease by body system or component › digestive system disorderstomach disordergastritis

Related subtypes (18): gastric ulcer, functional gastric disease, Dieulafoy lesion, pylorospasm, cascade stomach, pyloric stenosis, gastric dilatation, stomach diverticulosis, gastroesophageal reflux disease, hiatus hernia, stomach polyp, non-hypoproteinemic hypertrophic gastropathy, gastric neoplasm, angiodysplasia of stomach, achlorhydria, gastric intestinal metaplasia, gastric duplication, pyloric duplication

Subtypes (16): gastroduodenal Crohn disease, viral gastritis, eosinophilic gastritis, bacterial gastritis, fungal gastritis, lymphocytic gastritis, necrotizing gastritis, granulomatous gastritis, gastroduodenitis, alcoholic gastritis, chronic gastritis, gastric mucosal hypertrophy, chronic erosive gastritis, autoimmune gastritis, collagenous gastritis, pediatric collagenous gastritis

Genetics & variants

GWAS landscape

21 GWAS associations across 42 studies. Top hits map to 16 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
rs5511684611e-12ZNF385BG2.47
rs1897299208e-12CDH18T2.62
rs5315636741e-11SORCS2A3.86
rs1480924362e-11PVT1T2.72
rs5641448653e-11LINC01031T3.06
rs5484142953e-11KCNF1 - RPL6P4T1.8
chr6:326442573e-10T0.04
rs92743624e-10HLA-DQB1?0.95
rs118875341e-09ABCG8?1.11
rs1126141582e-08LINC02416?1.11
chr12:854215913e-08C1.9
rs38456594e-08ISCA1P6 - LINC01854?
chr1:1538970334e-08C1.09
rs69266207e-08CASC15?
rs64457972e-06ERC2 - CCDC66C1.4
rs15030592e-06CA10?1.28
rs109559712e-06COL14A1T1.32
rs81124492e-06CDC37T1.3
rs78269063e-06MTBPG1.32
rs110882264e-06CFAP298-TCP10L, TCP10LG1.3
rs9451449e-06LY86-AS1?1.26

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90432137Jiang Y2023116,382213,325A cross-disorder study to identify causal relationships, shared genetic variants, and genes across 21 digestive disorders.
GCST90473787UK Biobank Whole-Genome Sequencing Consortium202559,353399,087Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90667941UK Biobank Whole-Genome Sequencing Consortium202559,353399,087Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90129440Zorina-Lichtenwalter K202341,746179,970Genetic risk shared across 24 chronic pain conditions: identification and characterization with genomic structural equation modeling.
GCST90080208Backman JD202137,321345,285Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90084194Backman JD202137,321345,285Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90080206Backman JD202119,439366,238Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90084192Backman JD202119,439366,238Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90044139Jiang L202117,420438,928A generalized linear mixed model association tool for biobank-scale data.
GCST90726804Kim HI20268,51635,510Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding1
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic20

MAF distribution

BucketVariants
common (>=0.05)12
low_freq (0.01-0.05)0
rare (<0.01)6
unknown3

Functional consequences

ConsequenceCount
intron_variant12
intergenic_variant4
unknown3
non_coding_transcript_exon_variant1
missense_variant1

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs5511684612179810783G>A0.001intron_variantZNF385B1e-12Tier 4: intronic/intergenic
rs189729920520084119T>C0.001intergenic_variantCDH188e-12Tier 4: intronic/intergenic
rs53156367447318322A>C0intron_variantSORCS21e-11Tier 4: intronic/intergenic
rs1480924368127828407T>C0intron_variantPVT12e-11Tier 4: intronic/intergenic
rs5641448651193349223T>G0.001non_coding_transcript_exon_variantLINC010313e-11Tier 4: intronic/intergenic
rs548414295210969056T>A0.002intergenic_variantKCNF1 - RPL6P43e-11Tier 4: intronic/intergenic
chr6:326442573e-10Tier 4: intronic/intergenic
rs9274362632664709T>A,C0.05intron_variantHLA-DQB14e-10Tier 4: intronic/intergenic
rs11887534243839108G>A,C0.05missense_variantABCG81e-09Tier 1: coding
rs1126141581247357406C>A,T0.05intron_variantLINC024162e-08Tier 4: intronic/intergenic
chr12:854215913e-08Tier 4: intronic/intergenic
rs38456592128715434C>T0.05intron_variantISCA1P6 - LINC018544e-08Tier 4: intronic/intergenic
chr1:1538970334e-08Tier 4: intronic/intergenic
rs6926620621995317G>C0.05intron_variantCASC157e-08Tier 4: intronic/intergenic
rs6445797356529312C>A,G,T0.05intergenic_variantERC2 - CCDC662e-06Tier 4: intronic/intergenic
rs15030591752127096C>G0.05intron_variantCA102e-06Tier 4: intronic/intergenic
rs109559718120364107G>A,C0.05intron_variantCOL14A12e-06Tier 4: intronic/intergenic
rs81124491910409388G>A0.05intron_variantCDC372e-06Tier 4: intronic/intergenic
rs78269068120489483G>A0.05intron_variantMTBP3e-06Tier 4: intronic/intergenic
rs110882262132553221C>A,G0.05intergenic_variantCFAP298-TCP10L, TCP10L4e-06Tier 4: intronic/intergenic
rs94514466476045T>A,C,G0.05intron_variantLY86-AS19e-06Tier 4: intronic/intergenic

Genes & proteins

Mendelian disease overlap and somatic drivers

GenCC: 0 · Orphanet: 1 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0

Orphanet rare-disease linkage (cohort genes)

GeneOrphanet IDRare disease
COL14A1Orphanet:79501Punctate palmoplantar keratoderma type 1

Cohort genes → proteins

4 cohort genes, 3 distinct canonical proteins.

Evidence partition

SubsetGenes
gwas_only4

Cohort genes (full)

SymbolHGNCEnsemblUniProtNameEvidence
CA10HGNC:1369ENSG00000154975Q9NS85Carbonic anhydrase-related protein 10gwas
MRPL13HGNC:14278ENSG00000172172Q9BYD1Large ribosomal subunit protein uL13mgwas
COL14A1HGNC:2191ENSG00000187955Q05707Collagen alpha-1(XIV) chaingwas
LY86-AS1HGNC:26593ENSG00000216863LY86 antisense RNA 1gwas

Cohort function summary

Lead sentence per gene, UniProt-curated.

SymbolProtein nameFunction (lead sentence)
CA10Carbonic anhydrase-related protein 10Does not have a catalytic activity.
COL14A1Collagen alpha-1(XIV) chainPlays an adhesive role by integrating collagen bundles.

Protein-family classification

Druggable: 1 · Difficult: 0 · Unknown: 3 · Druggable fraction: 0.25

Family distribution

Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.

FamilyGenesFoldFDR
Antibody/Immunoglobulin17.3×0.260
Other/Unknown31.3×0.404

Per-gene assignment

SymbolFamilyDruggable?ECInterPro (top 3)
CA10Other/UnknownnoCA_dom, Carbonic_anhydrase_a-class, CA_dom_sf
MRPL13Other/UnknownnoRibosomal_uL13, Ribosomal_uL13_bact, Ribosomal_uL13_CS
COL14A1Antibody/ImmunoglobulinyesVWF_A, FN3_dom, Collagen
LY86-AS1Other/Unknownno

Expression context

Cohort genes with no expression data: 0.

4 cohort genes are a single-cell marker in ≥1 SCXA experiment.

Breadth distribution (Bgee present_calls)

BucketGenes
narrow (1-5 tissues)0
moderate (6-20)0
broad (>20)4
unknown0

Top tissues across cohort

TissueCohort genes
cerebellar cortex1
cerebellar hemisphere1
cerebellum1
adrenal tissue1
ganglionic eminence1
mucosa of transverse colon1
descending thoracic aorta1
popliteal artery1
right coronary artery1
Brodmann (1909) area 91
colonic epithelium1
primordial germ cell in gonad1

Per-gene tissue summary (top 30)

SymbolBgee breadthFANTOM5 breadthSCXATop tissues
CA10167tissue_specificmarkercerebellar cortex, cerebellar hemisphere, cerebellum
MRPL13284ubiquitousmarkermucosa of transverse colon, adrenal tissue, ganglionic eminence
COL14A1245broadmarkerdescending thoracic aorta, right coronary artery, popliteal artery
LY86-AS1154tissue_specificmarkerprimordial germ cell in gonad, colonic epithelium, Brodmann (1909) area 9

Protein interactions among cohort

Intra-cohort edges: 0.

Hub genes (top 10 by interactor count)

SymbolInteractor count
MRPL135,398
CA102,597
COL14A11,991
LY86-AS10

Structural data

PDB: 1 · AlphaFold-only: 2 · No structure: 1

Cohort genes with PDB structures (top 30)

SymbolUniProtPDB entries
MRPL13Q9BYD172

AlphaFold-only cohort genes (top 30 by pLDDT)

SymbolUniProtpLDDT
CA10Q9NS8585.65
COL14A1Q0570774.06

Function

Pathway analysis

Distinct Reactome pathways touched by cohort: 11. Enrichment computed across 4 evidence-associated genes (2 with Reactome annotation).

Pathways by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 2 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

PathwayCohort genesFoldFDRSample cohort genes
Collagen chain trimerization1129.8×0.022COL14A1
Assembly of collagen fibrils and other multimeric structures1100.2×0.022COL14A1
Collagen degradation187.8×0.022COL14A1
Collagen biosynthesis and modifying enzymes185.2×0.022COL14A1
Mitochondrial translation168.8×0.022MRPL13
Mitochondrial translation initiation163.4×0.022MRPL13
Mitochondrial translation elongation163.4×0.022MRPL13
Mitochondrial ribosome-associated quality control161.4×0.022MRPL13
Mitochondrial translation termination154.9×0.022MRPL13
Translation131.0×0.035MRPL13
Metabolism of proteins16.2×0.155MRPL13

GO biological processes by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 3 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

GO termCohort genesFoldFDRSample cohort genes
regulation of cell growth involved in cardiac muscle cell development15617.3×0.002COL14A1
ventricular cardiac muscle tissue development1702.2×0.007COL14A1
homeostasis of number of cells within a tissue1147.8×0.022COL14A1
collagen fibril organization174.9×0.029COL14A1
negative regulation of translation165.3×0.029MRPL13
mitochondrial translation157.9×0.029MRPL13
extracellular matrix organization140.7×0.033COL14A1
translation134.2×0.033MRPL13
cell-cell adhesion133.8×0.033COL14A1
brain development126.5×0.037CA10

Therapeutics

Drugs indicated for this disease

0 approved, 6 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
AmoxicillinPhase 3 (in late-stage trials)
ClarithromycinPhase 3 (in late-stage trials)
EsomeprazolePhase 3 (in late-stage trials)
LansoprazolePhase 3 (in late-stage trials)
RebamipidePhase 3 (in late-stage trials)
RecoflavonePhase 3 (in late-stage trials)

Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Omeprazole.

Drug target analysis

Approved (phase 4): 0 · Phase ≥3: 0 · Phased (≥1): 0 · Undrugged: 4

Druggability breadth: 1 of 4 evidence-associated genes (25%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).

Top cohort targets by molecule count

SymbolMoleculesMax phase
CA1000
MRPL1300
COL14A100
LY86-AS100

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 0.

Cohort genes with ChEMBL bioactivity (full, sorted by assay count)

SymbolAssaysType breakdown
COL14A11Binding:1

Pharmacogenomics

Cohort genes with a PharmGKB record: 4; with CPIC/DPWG dosing guidelines: 0.

No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).

Chemical tractability of cohort targets

0 approved/phased compounds have measured bioactivity against a cohort gene (and aren’t yet in disease-level trials). This is a research / tractability signal, NOT a therapeutic recommendation — a bioactivity row often reflects off-target or screening binding (e.g. promiscuous kinase inhibitors against a cohort kinase), implying no disease mechanism.

Druggability pyramid

Cohort genes binned by druggability tier (high → low):

TierDefinitionGenesSymbols
AApproved (phase 4 drug)0
BPhased (≥1) drug, not yet approved0
CDruggable family + PDB, no drug0
DDruggable family + AlphaFold only, no drug1COL14A1
EDifficult family or no structure, no drug3CA10, MRPL13, LY86-AS1

Undrugged target profiles

4 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).

SymbolChEMBL assaysDrugged partners (top 3)
CA100
MRPL130
COL14A11
LY86-AS10

Clinical trials & evidence

Clinical trials

Clinical trials: 86.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified39
PHASE315
PHASE414
PHASE18
PHASE27
PHASE2/PHASE32
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07139366PHASE4RECRUITINGSaccharomyces Boulardii Combined With Bismuth Quadruple Therapy for Helicobacter Pylori Rescue Treatment
NCT01190657PHASE4COMPLETEDEfficacy and Safety of Teprenone in Patients With Acute Gastritis, Acute Gastric Lesion of Chronic Gastritis With Acute Exacerbation or Gastric Ulcer
NCT01817556PHASE4COMPLETEDA Study to Evaluate the Efficacy and of Stillen Tab. and to Demonstrate the Non-inferiority of Stillen Tab.
NCT02175186PHASE4COMPLETEDEffect of ALBIS on Gastroduodenal Mucosal Injury in Patients Receiving Dual Antiplatelet Therapy After Percutaneous Coronary Intervention
NCT02296021PHASE4COMPLETEDHelicobacter Pylori Eradication With Berberine Quadruple Therapy Versus Bismuth-containing Quadruple Therapy
NCT02356679PHASE4COMPLETEDEfficacy and Safety of Eupasidin-s Tab.(EUPASIDIN-S) in Gastritis Patients
NCT02393430PHASE4COMPLETEDClinical Effect of Rebamipide on Chronic Gastritis
NCT02633930PHASE4COMPLETEDHelicobacter Pylori Eradication With Berberine Quadruple Therapy Versus Clarithromycin Quadruple Therapy
NCT03609892PHASE4COMPLETEDHelicobacter Rescue Therapy With Berberine Plus Amoxicillin Quadruple Therapy Versus Tetracycline Plus Furazolidone Quadruple Therapy
NCT03857425PHASE4COMPLETEDHelicobacter Pylori Eradication With Clostridum Butyricum Capsule and Bacillus Coagulans Tablets
NCT04678492PHASE4COMPLETEDHelicobacter Rescue Therapy With High-dose Esomeprazole and Amoxicillin Dual Therapy Versus Bismuth-containing Quadruple Therapy
NCT05072938PHASE4COMPLETEDClinical Trial to Compare Rebamipide/Nizatidine Combination Therapy With Nizatidine Monotherapy in Patients With Gastritis
NCT05237115PHASE4COMPLETEDHelicobacter Pylori Eradication With Probiotics Combined With Triple Therapy Versus Bismuth-containing Quadruple Therapy
NCT05742568PHASE4COMPLETEDEffects of High-dose Dual Therapy and Bismuth Quadruple Therapy for Helicobacter Pylori Eradication on Intestinal Microecology
NCT00132171PHASE3COMPLETEDHelicobacter Pylori Eradication With a New Sequential Treatment
NCT00149084PHASE3UNKNOWNTailored Treatment of H. Pylori Infection Based Polymorphisms of CYP2C19 and 23S rRNA of H. Pylori
NCT00197418PHASE2/PHASE3UNKNOWNSecond Line Therapy for the Cure of Helicobacter Pylori (H. Pylori) Infection
NCT01813812PHASE3UNKNOWNA Study to Evaluate the Efficacy and Safety of DA-6034 and to Demonstrate the Non-inferiority of DA-6034
NCT01828645PHASE2/PHASE3COMPLETEDResidual Gastric Volume After the Ingestion of a Beverage Containing Carbohydrates Plus Whey Protein
NCT02246439PHASE3COMPLETEDBEKINDA (Ondansetron 24 mg Bimodal Release Tablets) for Vomiting Due to Presumed Acute Gastroenteritis or Gastritis
NCT02282670PHASE3UNKNOWNA Study to Evaluate the Efficacy and Safety of DA-5204
NCT03184415PHASE3TERMINATEDEfficacy and Safety of DWC20155/DWC20156 Combination Therapy in Patients With Gastritis
NCT03443804PHASE3COMPLETEDTo Evaluate the Efficacy and Safety of DW-1401 in Acute and Chronic Gastritis Patients
NCT04066530PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of AD-203
NCT04189705PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of MCT-SR in Patients With Gastritis
NCT04255589PHASE3COMPLETEDA Clinical Trial to Evaluate the Efficacy and Safety of CKD-495
NCT04341454PHASE3COMPLETEDStudy to Evaluate the Efficacy and Safety of DWP14012 in Patients With Acute or Chronic Gastritis
NCT05024721PHASE3COMPLETEDStudy to Evaluate the Efficacy and Safety of HIP2101 in Patients With Acute or Chronic Gastritis
NCT05163756PHASE3COMPLETEDTo Evaluate the Efficacy and Safety of DW1903 in Acute and Chronic Gastritis Patient
NCT06151210PHASE3COMPLETEDClinical Trial to Evaluate the Efficacy and Safety of DA-5219 in Patients With Acute or Chronic Gastritis
NCT06576882PHASE3COMPLETED7 Days vs. 14 Days of Vonoprazan-based Triple Therapy for H. Pylori Eradication
NCT00854880PHASE2COMPLETEDA Clinical Trial to Evaluate the Efficacy and Safety of PDC-339 for the Treatment of Acute Erosive Gastritis
NCT01578811PHASE2COMPLETEDStudy to Assess the Efficacy and Safety of SK-MS10 in Subjects With Acute and Chronic Gastritis
NCT02353039PHASE2UNKNOWNPhase II Study to Evaluate the Efficacy and Safety of GC6101A in Subjects With Gastritis
NCT03428568PHASE2UNKNOWNSafety Trial of Herbal Melanin in Gastritis Patients
NCT03437785PHASE2COMPLETEDClinical Trial to Evaluate the Efficacy and Safety of CKD-495 Tablet
NCT04672018PHASE2COMPLETEDEfficacy and Safety of Houtou Jianweiling Tablet in the Treatment of Chronic Non-Atrophic Gastritis
NCT07139886PHASE2COMPLETEDA Study to Evaluate the Safety and Efficacy of DA9601 for Acute and Chronic Gastritis and to Determine the Optimal Clinical Dosage and Administration
NCT07385248PHASE1NOT_YET_RECRUITINGA Clinical Trial to Assess the Pharmacokinetics and Safety of AD-229 Compared to AD-2291 in Healthy Adults
NCT00613665PHASE1COMPLETEDSafety and Immunogenicity of Chiron’s Investigational H. Pylori Vaccine in Healthy Adults

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
AMOXICILLIN410
BERBERINE49
CLARITHROMYCIN46
FURAZOLIDONE43
TETRACYCLINE43
ESOMEPRAZOLE42
LANSOPRAZOLE42
VONOPRAZAN42
RABEPRAZOLE41
REBAMIPIDE36
RECOFLAVONE31
TEPRENONE31
IRSOGLADINE MALEATE11
CHEMBL313767307
CHEMBL170333603
CHEMBL137473803
CHEMBL157216703
CHEMBL428387501