abnormal palatine bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of either of two irregularly L-shaped bones located posterior to the maxilla that in part forms the back of the hard palate, part of the nasal cavity and part of the floor of the orbits (Mammalian Phenotype Ontology, MP_0005249)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005249
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Genes

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

Symbol Name
ALX1 ALX homeobox 1
ANXA1 annexin A1
ARID5B AT rich interactive domain 5B (MRF1-like)
BAZ1B bromodomain adjacent to zinc finger domain, 1B
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
ECE1 endothelin converting enzyme 1
EDNRA endothelin receptor type A
EDNRB endothelin receptor type B
EYA1 EYA transcriptional coactivator and phosphatase 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FOXC2 forkhead box C2
FOXF2 forkhead box F2
FOXI3 forkhead box I3
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
GSC goosecoid homeobox
IRF6 interferon regulatory factor 6
JAG2 jagged 2
MN1 meningioma (disrupted in balanced translocation) 1
MNT MAX network transcriptional repressor
MSX1 msh homeobox 1
PAX9 paired box 9
PKDCC protein kinase domain containing, cytoplasmic
PRRX1 paired related homeobox 1
RSPO2 R-spondin 2
SCHIP1 schwannomin interacting protein 1
SGPL1 sphingosine-1-phosphate lyase 1
TBX22 T-box 22
TCOF1 Treacher Collins-Franceschetti syndrome 1
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
WDR19 WD repeat domain 19