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ULK1 and Crohn disease are reported together in 1 article.

Gene

ULK1

HGNC
HGNC:12558
9articles
9mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype

Crohn disease

435articles
435mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

1 records shown · first 60

ULK1-mediated phosphorylation of ATG16L1 promotes xenophagy, but destabilizes the ATG16L1 Crohn's mutant.

PMID 31267703 | PMCID PMC6607016 | DOI 10.15252/embr.201846885 · EMBO reports · 2019 · 4 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneULK1“Here we show that ULK1 kinase directly phosphorylates ATG16L1 in response to infection and starvation.”0.98hgnc_dict_v1
phenotypeCrohn disease“ATG16L1 polymorphisms have been linked to the development of Crohn's disease (CD), and phosphorylation of CD-associated ATG16L1 T300A (caATG16L1) has been hypothesized to contribute to cleavage and autophagy dysfunction.”0.93phenotype_alias_lexicon_v2
geneATG16L1“ULK1-mediated phosphorylation of ATG16L1 promotes xenophagy, but destabilizes the ATG16L1 Crohn's mutant.”0.98hgnc_dict_v1
variantT300A“ATG16L1 polymorphisms have been linked to the development of Crohn's disease (CD), and phosphorylation of CD-associated ATG16L1 T300A (caATG16L1) has been hypothesized to contribute to cleavage and autophagy dysfunction.”0.82literature_variant_regex_v2