abnormality of the ischium Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the ischium, which forms the lower and back part of the hip bone. (Human Phenotype Ontology, HP_0003174)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003174
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Genes

9 genes associated with the abnormality of the ischium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
COL11A1 collagen, type XI, alpha 1
COL11A2 collagen, type XI, alpha 2
COL2A1 collagen, type II, alpha 1
INPPL1 inositol polyphosphate phosphatase-like 1
KAT6B K(lysine) acetyltransferase 6B
LIFR leukemia inhibitory factor receptor alpha
TBX15 T-box 15
TRIP11 thyroid hormone receptor interactor 11