← New search
Gene profile

ULK1

HGNC:12558 · SaudiVarKB evidence summary derived from retained literature mentions.

9Gene mentions
9Publications
0Linked variants
6Associated phenotypes

Associated phenotypes

Co-mentioned in ULK1 publications
PhenotypeIdentifierArticlesMentions
intellectual disabilityHP:000124922
cardiomyopathyHP:000163811
Parkinson disease11
developmental delayHP:000126311
Noonan syndrome11
Crohn disease11

Linked variants

Variants normalized to ULK1
VariantHGVS / rsIDArticlesMentions

No normalized variants are linked to this gene.

Population context

Reported in the same publications
Country / regionGroupCohortArticles
Not specified1
Not specified1001

Supporting publications

9 records
  1. 2026Resveratrol alleviates neurological disorders and motor dysfunction in 3-NP induced- Huntington's Disease in rats: Role of activating AMPK/SIRT1/ULK1 autophagy pathway.NeuropharmacologyPubMed ↗
  2. 2025Cognitive and psychotic effects of ketamine "short- vs. long-term" therapy in a rat model of depression: Hippocampal TrkB/Akt/GSK-3β/mTOR/autophagy trajectories.Progress in neuro-psychopharmacology & biological psychiatryPubMed ↗
  3. 2024Trigonelline Chloride Ameliorated Triphenyltin-Induced Testicular Autophagy, Inflammation, and Apoptosis: Role of Recovery.Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of CanadaPubMed ↗
  4. 2024The autophagy-mediated mechanism via TSC1/mTOR signaling pathway in thiram-induced tibial dyschondroplasia of broilers.The Science of the total environmentPubMed ↗
  5. 2023Bisphenol-A exposure alters liver, kidney, and pancreatic Klotho expression by HSP60-activated mTOR/autophagy pathway in male albino rats.Cellular and molecular biology (Noisy-le-Grand, France)PubMed ↗
  6. 2021Investigation of the specificity and mechanism of action of the ULK1/AMPK inhibitor SBI-0206965.The Biochemical journalPubMed ↗
  7. 2020Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy.Circulation. Genomic and precision medicinePubMed ↗
  8. 2019ULK1-mediated phosphorylation of ATG16L1 promotes xenophagy, but destabilizes the ATG16L1 Crohn's mutant.EMBO reportsPubMed ↗
  9. 2011Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects.Molecular cytogeneticsPubMed ↗