abnormal palate bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the maxillary or palatine shelves that comprise the bones of the hard palate (Mammalian Phenotype Ontology, MP_0009891)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009891
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Genes

36 gene mutations causing the abnormal palate bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARID5B AT rich interactive domain 5B (MRF1-like)
BMP7 bone morphogenetic protein 7
BNC2 basonuclin 2
CDON cell adhesion associated, oncogene regulated
CSRNP1 cysteine-serine-rich nuclear protein 1
CYP51A1 cytochrome P450, family 51, subfamily A, polypeptide 1
DLX2 distal-less homeobox 2
DLX5 distal-less homeobox 5
EDNRB endothelin receptor type B
EYA1 EYA transcriptional coactivator and phosphatase 1
EYA4 EYA transcriptional coactivator and phosphatase 4
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FOXC2 forkhead box C2
FOXF2 forkhead box F2
GLG1 golgi glycoprotein 1
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
HAND2 heart and neural crest derivatives expressed 2
IRF6 interferon regulatory factor 6
JAG2 jagged 2
MN1 meningioma (disrupted in balanced translocation) 1
MSX1 msh homeobox 1
PAX6 paired box 6
PAX9 paired box 9
PDGFC platelet derived growth factor C
PDS5B PDS5 cohesin associated factor B
PRRX1 paired related homeobox 1
RSPO2 R-spondin 2
SCHIP1 schwannomin interacting protein 1
SGPL1 sphingosine-1-phosphate lyase 1
TBX22 T-box 22
TGFB2 transforming growth factor, beta 2
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
WDR19 WD repeat domain 19
ZEB1 zinc finger E-box binding homeobox 1