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
About your search
GFAP and COVID-19 are reported together in 1 article.
Gene
GFAP
- HGNC
- HGNC:4235
53articles
53mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
COVID-19
1,317articles
1,317mentions
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 60Cytokine Storm and Neuropathological Alterations in Patients with Neurological Manifestations of COVID-19.
PMID 36089786 | DOI 10.2174/1567205019666220908084559 · Current Alzheimer research · 2022 · 7 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | GFAP | “Biomarker studies on CSF and plasma and serum from COVID-19 patients have also shown a high level of IL-6, intrathecal IgG, neurofilament light chain (NFL), glial fibrillary acidic protein (GFAP), and tau protein.” | 0.98 | hgnc_dict_v1 |
| phenotype | COVID-19 | “Cytokine Storm and Neuropathological Alterations in Patients with Neurological Manifestations of COVID-19.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | stroke | “Neurological COVID-19 manifestations include loss of smell and taste, headache, dizziness, stroke, and potentially fatal encephalitis.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | amyotrophic lateral sclerosis | “The association of the aforementioned cytokines with the pathogenesis of neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, Huntington's disease, and amyotrophic lateral sclerosis, may increase COVID-19 patients' risk of developing neurodegenerative diseases.” | 0.98 | phenotype_alias_lexicon_v2 |