abnormal exoccipital bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly 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_0000080)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000080
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10 gene mutations causing the abnormal exoccipital bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDX1 caudal type homeobox 1
FOXC2 forkhead box C2
HECTD1 HECT domain containing E3 ubiquitin protein ligase 1
HHAT hedgehog acyltransferase
HOXA1 homeobox A1
NKX3-2 NK3 homeobox 2
PCGF2 polycomb group ring finger 2
PSIP1 PC4 and SFRS1 interacting protein 1
TCF15 transcription factor 15 (basic helix-loop-helix)
TMEM107 transmembrane protein 107