Occupation-related stress disorder

disease
On this page

Summary

Occupation-related stress disorder (MONDO:0005467) is a disease with 1 cohort gene (1 GWAS associations across 1 studies) and 7 clinical trials.

At a glance

  • Cohort genes: 1
  • GWAS associations: 1
  • Clinical trials: 7

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameoccupation-related stress disorder
Mondo IDMONDO:0005467
SNOMED CT10586006
UMLSC0520683
MedGen636163
Is cancer (heuristic)no

Data availability: 1 GWAS association (1 study).

Disease family

Classification path: disease › human disease › disease by etiologic mechanism › disease of primarily extrinsic mechanism › occupational disorder › occupation-related stress disorder

Related subtypes (2): occupational dermatitis, occupational lung disease

Genetics & variants

GWAS landscape

1 GWAS associations across 1 studies. Top hits map to 1 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
rs132199577e-07USTA0.08

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST001983Sulkava S201300Genome-wide scan of job-related exhaustion with three replication studies implicate a susceptibility variant at the UST gene locus.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding0
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic1

MAF distribution

BucketVariants
common (>=0.05)1
low_freq (0.01-0.05)0
rare (<0.01)0
unknown0

Functional consequences

ConsequenceCount
intron_variant1

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs132199576148949693G>A0.144intron_variantUST7e-07Tier 4: intronic/intergenic

Genes & proteins

Mendelian disease overlap and somatic drivers

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

Cohort genes → proteins

1 cohort genes, 1 distinct canonical proteins.

Evidence partition

SubsetGenes
gwas_only1

Cohort genes (full)

SymbolHGNCEnsemblUniProtNameEvidence
USTHGNC:17223ENSG00000111962Q9Y2C2Uronyl 2-sulfotransferasegwas

Cohort function summary

Lead sentence per gene, UniProt-curated.

SymbolProtein nameFunction (lead sentence)
USTUronyl 2-sulfotransferaseSulfotransferase that utilizes 3’-phospho-5’-adenylyl sulfate (PAPS) to catalyze the transfer of a sulfo group to the 2-OH position of uronyl residues in glycosaminoglycan chains.

Protein-family classification

Druggable: 0 · Difficult: 0 · Unknown: 1 · Druggable fraction: 0.0

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
Other/Unknown11.8×0.558

Per-gene assignment

SymbolFamilyDruggable?ECInterPro (top 3)
USTOther/UnknownnoSulfotransferase, Heparan_SO4_2-O-STrfase, P-loop_NTPase

Expression context

Cohort genes with no expression data: 0.

1 cohort gene 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)1
unknown0

Top tissues across cohort

TissueCohort genes
adrenal tissue1
calcaneal tendon1
pons1

Per-gene tissue summary (top 30)

SymbolBgee breadthFANTOM5 breadthSCXATop tissues
UST261ubiquitousmarkerpons, calcaneal tendon, adrenal tissue

Protein interactions among cohort

Intra-cohort edges: 0.

Hub genes (top 10 by interactor count)

SymbolInteractor count
UST413

Structural data

PDB: 0 · AlphaFold-only: 1 · No structure: 0

AlphaFold-only cohort genes (top 30 by pLDDT)

SymbolUniProtpLDDT
USTQ9Y2C279.64

Function

Pathway analysis

Distinct Reactome pathways touched by cohort: 2. Enrichment computed across 1 evidence-associated genes (1 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 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

PathwayCohort genesFoldFDRSample cohort genes
DS-GAG biosynthesis1951.7×0.002UST
CS-GAG biosynthesis1543.8×0.002UST

GO biological processes by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

GO termCohort genesFoldFDRSample cohort genes
dermatan sulfate proteoglycan biosynthetic process11685.2×0.002UST
regulation of axonogenesis1887.0×0.002UST
chondroitin sulfate proteoglycan biosynthetic process1624.1×0.002UST
establishment of cell polarity1383.0×0.003UST

Therapeutics

Drug target analysis

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

Druggability breadth: 0 of 1 evidence-associated genes (0%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).

Top cohort targets by molecule count

SymbolMoleculesMax phase
UST00

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 0.

Pharmacogenomics

Cohort genes with a PharmGKB record: 1; 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 drug0
EDifficult family or no structure, no drug1UST

Undrugged target profiles

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

SymbolChEMBL assaysDrugged partners (top 3)
UST0

Clinical trials & evidence

Clinical trials

Clinical trials: 7.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified7

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06488547Not specifiedRECRUITINGStress and Musculoskeletal Health in Employees
NCT02228161Not specifiedUNKNOWNThe Effects of Yoga in Mental Health Professional Helpers
NCT02480855Not specifiedCOMPLETEDEarly Identification of Persons at Risk for Sick-leave Due to Work-related Stress
NCT03077568Not specifiedCOMPLETEDEvaluation of a Web Application That Supports Behavior Change in Work Related Stress
NCT03235206Not specifiedUNKNOWNMassage Therapy and the Well-Being of Police Officers
NCT03634410Not specifiedUNKNOWNSeniorWorkingLife (Danish Title: SeniorArbejdsLiv)
NCT07474766Not specifiedCOMPLETEDDigital Counseling Community for Burnout Prevention
  • Cohort genes: UST