abnormality of the pubic bone Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the the pubic bone, i.e., of the ventral and anterior of the three principal components (publis, ilium, ischium) of the hip bone. (Human Phenotype Ontology, HP_0003172)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003172
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Genes

15 genes associated with the abnormality 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
DYM dymeclin
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
GSC goosecoid homeobox
INPPL1 inositol polyphosphate phosphatase-like 1
KAT6B K(lysine) acetyltransferase 6B
MATN3 matrilin 3
RUNX2 runt-related transcription factor 2
SETBP1 SET binding protein 1
TBX15 T-box 15
WNT7A wingless-type MMTV integration site family, member 7A