small exoccipital bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the bone or region on the lateral sides of the great foremen of the skull, which often forms a part of the occipital in the adult, but is usually distinct in the young (Mammalian Phenotype Ontology, MP_0004445)
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4 gene mutations causing the small exoccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXC2 forkhead box C2
HHAT hedgehog acyltransferase
NKX3-2 NK3 homeobox 2
PSIP1 PC4 and SFRS1 interacting protein 1