abnormal sternal ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any anomaly in the formation of the bony substance of the sternum. (Human Phenotype Ontology, HP_0011863)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011863
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Genes

6 genes associated with the abnormal sternal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CD96 CD96 molecule
FIG4 FIG4 phosphoinositide 5-phosphatase
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
ORC1 origin recognition complex, subunit 1
ORC6 origin recognition complex, subunit 6
SOX9 SRY (sex determining region Y)-box 9