shallow orbits Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced depth of the orbits associated with prominent-appearing ocular globes. (Human Phenotype Ontology, HP_0000586)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000586
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Genes

12 genes associated with the shallow orbits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FBN1 fibrillin 1
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FLNB filamin B, beta
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
PLOD3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
SETBP1 SET binding protein 1
SKI SKI proto-oncogene
TWIST1 twist family bHLH transcription factor 1