Advanced search
Combine gene, variant, phenotype, region and year filters
Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.
Transparent by designEvery result links extracted entities to its source sentence and publication identifier.
Knowledge-base search
Publications
2 records shown · first 60A Cell Specific Effect of MBOAT7 MAFLD-risk Variant on Immune Cells.
PMID 38682204 | DOI 10.31083/j.fbl2904148 · Frontiers in bioscience (Landmark edition) · 2024 · 2 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| variant | rs8736 | “The membrane bound O-acyltransferase domain containing 7 (MBOAT7) rs8736 metabolic-dysfunction-associated fatty liver disease (MAFLD)-risk variant was recently reported to be a negative regulator of toll-like receptors (TLRs) signalling in macrophages.” | 0.90 | hgvs_regex_v1 |
| gene | MBOAT7 | “A Cell Specific Effect of MBOAT7 MAFLD-risk Variant on Immune Cells.” | 0.98 | hgnc_dict_v1 |
A metabolic associated fatty liver disease risk variant in MBOAT7 regulates toll like receptor induced outcomes.
PMID 36473860 | PMCID PMC9726889 | DOI 10.1038/s41467-022-35158-9 · Nature communications · 2022 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| variant | rs8736 | “These outcomes are further modulated by the MBOAT7 rs8736 (T) MAFLD risk variant.” | 0.90 | hgvs_regex_v1 |
| gene | MBOAT7 | “A metabolic associated fatty liver disease risk variant in MBOAT7 regulates toll like receptor induced outcomes.” | 0.98 | hgnc_dict_v1 |
| phenotype | COVID-19 | “The breakdown of toll-like receptor (TLR) tolerance results in tissue damage, and hyperactivation of the TLRs and subsequent inflammatory consequences have been implicated as risk factors for more severe forms of disease and poor outcomes from various diseases including COVID-19 and metabolic (dysfunction) associated fatty liver disease (MAFLD).” | 0.98 | phenotype_alias_lexicon_v2 |