Congenital Absence Of Mandible Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0685776
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Genes

14 genes associated with the disease Congenital Absence Of Mandible in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CDC45 cell division cycle 45
CDC6 cell division cycle 6
CDT1 chromatin licensing and DNA replication factor 1
CHUK conserved helix-loop-helix ubiquitous kinase
COX7B cytochrome c oxidase subunit VIIb
FAM20C family with sequence similarity 20, member C
GMNN geminin, DNA replication inhibitor
HCCS holocytochrome c synthase
NDUFB11 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 11, 17.3kDa
ORC1 origin recognition complex, subunit 1
ORC4 origin recognition complex, subunit 4
ORC6 origin recognition complex, subunit 6
OTX2 orthodenticle homeobox 2
PRRX1 paired related homeobox 1