aplasia/hypoplasia of the pubic bone Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the pubic bone. (Human Phenotype Ontology, HP_0009104)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009104
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Genes

9 genes associated with the aplasia/hypoplasia of the pubic bone 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
COL11A2 collagen, type XI, alpha 2
COL2A1 collagen, type II, alpha 1
INPPL1 inositol polyphosphate phosphatase-like 1
KAT6B K(lysine) acetyltransferase 6B
MATN3 matrilin 3
SETBP1 SET binding protein 1
TBX15 T-box 15
WNT7A wingless-type MMTV integration site family, member 7A