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.
About your search

NEK10 and cystic fibrosis are reported together in 1 article.

Gene

NEK10

HGNC
HGNC:18592
4articles
4mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
157articles
157mentions
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

A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearance.

PMID 31959991 | PMCID PMC7018620 | DOI 10.1038/s41591-019-0730-x · Nature medicine · 2020 · 4 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneNEK10“A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearance.”0.98hgnc_dict_v1
phenotypecystic fibrosis“Mucociliary clearance, the physiological process by which mammalian conducting airways expel pathogens and unwanted surface materials from the respiratory tract, depends on the coordinated function of multiple specialized cell types, including basal stem cells, mucus-secreting goblet cells, motile ciliated cells, cystic fibrosis transmembrane conductance regulator (CFTR)-rich ionocytes, and immune cells1,2.”0.98phenotype_alias_lexicon_v2
geneCFTR“Mucociliary clearance, the physiological process by which mammalian conducting airways expel pathogens and unwanted surface materials from the respiratory tract, depends on the coordinated function of multiple specialized cell types, including basal stem cells, mucus-secreting goblet cells, motile ciliated cells, cystic fibrosis transmembrane conductance regulator (CFTR)-rich ionocytes, and immune cells1,2.”0.98hgnc_dict_v1
phenotypeprimary ciliary dyskinesia“Bronchiectasis, a syndrome of pathological airway dilation associated with impaired mucociliary clearance, may occur sporadically or as a consequence of Mendelian inheritance, for example in cystic fibrosis, primary ciliary dyskinesia (PCD), and select immunodeficiencies3.”0.98phenotype_alias_lexicon_v2