Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
0.310 Biomarker MGD Through whole-genome sequencing analysis, we report that a homozygous splice site mutation in coiled-coil domain containing 39 (<i>Ccdc39</i>) is responsible for early postnatal hydrocephalus in the <i>progressive hydrocephal</i><i>us</i> (<i>prh</i>) mouse mutant. 29317443

2018

Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
0.310 Biomarker MGD Focusing forward genetics: a tripartite ENU screen for neurodevelopmental mutations in the mouse. 21515572

2011