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Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

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CDK6 and neurodevelopmental disorder are reported together in 1 article.

Gene

CDK6

5articles

5mentions

0variants with confirmed gene link

Most co-reported phenotypes (articles)

Phenotype

450articles

450mentions

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.

1 records shown · first 60

PMID 25951892 | PMCID PMC4315316 | DOI 10.1186/1755-8794-8-S1-S4 · BMC medical genomics · 2015 · 11 validated mentions

Evidence preview

Type	Entity	Source evidence	Confidence	Extractor
gene	CDK6	“Twelve MCPH loci (MCPH1-MCPH12) have been mapped to date from various populations around the world and contain the following genes: Microcephalin, WDR62, CDK5RAP2, CASC5, ASPM, CENPJ, STIL, CEP135, CEP152, ZNF335, PHC1 and CDK6.”	0.98	hgnc_dict_v1
phenotype	neurodevelopmental disorder	“Autosomal recessive primary microcephaly (MCPH) is a neurodevelopmental disorder that is characterised by microcephaly present at birth and non-progressive mental retardation.”	0.98	phenotype_alias_lexicon_v2
gene	WDR62	“Twelve MCPH loci (MCPH1-MCPH12) have been mapped to date from various populations around the world and contain the following genes: Microcephalin, WDR62, CDK5RAP2, CASC5, ASPM, CENPJ, STIL, CEP135, CEP152, ZNF335, PHC1 and CDK6.”	0.98	hgnc_dict_v1
gene	CDK5RAP2	“Twelve MCPH loci (MCPH1-MCPH12) have been mapped to date from various populations around the world and contain the following genes: Microcephalin, WDR62, CDK5RAP2, CASC5, ASPM, CENPJ, STIL, CEP135, CEP152, ZNF335, PHC1 and CDK6.”	0.98	hgnc_dict_v1