CDCA8, cell division cycle associated 8, 55143

N. diseases: 41; N. variants: 13
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1563716
Disease: Thyroid Dysgenesis
Thyroid Dysgenesis
0.310 Biomarker disease GENOMICS_ENGLAND Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis. 29546359 2018
CUI: C1563716
Disease: Thyroid Dysgenesis
Thyroid Dysgenesis
0.310 GeneticVariation disease BEFREE We identified the novel missense mutations p.S148F, p.R114Q and p.L177W in the BOREALIN gene in TD-affected families. 28025328 2017