aplasia/hypoplasia of the sternum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006714
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Genes

13 genes associated with the aplasia/hypoplasia of the sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
FIG4 FIG4 phosphoinositide 5-phosphatase
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NIPBL Nipped-B homolog (Drosophila)
NOG noggin
ORC1 origin recognition complex, subunit 1
ORC6 origin recognition complex, subunit 6
RBM10 RNA binding motif protein 10
SETBP1 SET binding protein 1
SOX9 SRY (sex determining region Y)-box 9