rib fusion Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Complete or partial merging of adjacent ribs. (Human Phenotype Ontology, HP_0000902)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000902
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Genes

10 genes associated with the rib fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANKRD11 ankyrin repeat domain 11
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
DLL3 delta-like 3 (Drosophila)
GLI3 GLI family zinc finger 3
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
RECQL4 RecQ protein-like 4
ROR2 receptor tyrosine kinase-like orphan receptor 2
SOX2 SRY (sex determining region Y)-box 2
TBX6 T-box 6
TMCO1 transmembrane and coiled-coil domains 1