aplasia/hypoplasia involving the pelvis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009103
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Genes

32 genes associated with the aplasia/hypoplasia involving the pelvis 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
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
BMPR1B bone morphogenetic protein receptor, type IB
CANT1 calcium activated nucleotidase 1
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COL11A2 collagen, type XI, alpha 2
COL2A1 collagen, type II, alpha 1
COMP cartilage oligomeric matrix protein
CTC1 CTS telomere maintenance complex component 1
CUL7 cullin 7
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
FGFR3 fibroblast growth factor receptor 3
IDUA iduronidase, alpha-L-
IFT140 intraflagellar transport 140
IHH indian hedgehog
INPPL1 inositol polyphosphate phosphatase-like 1
KAT6B K(lysine) acetyltransferase 6B
MATN3 matrilin 3
MMP9 matrix metallopeptidase 9
NSDHL NAD(P) dependent steroid dehydrogenase-like
POC1A POC1 centriolar protein A
RUNX2 runt-related transcription factor 2
SETBP1 SET binding protein 1
SHOX short stature homeobox
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC39A13 solute carrier family 39 (zinc transporter), member 13
TBX15 T-box 15
TRAPPC2 trafficking protein particle complex 2
TRPV4 transient receptor potential cation channel, subfamily V, member 4
WNT3 wingless-type MMTV integration site family, member 3
WNT7A wingless-type MMTV integration site family, member 7A