decreased palatine bone horizontal plate size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the bony plate of the palatine bone that normally fuses with maxillary shelf to form secondary (hard) palate (Mammalian Phenotype Ontology, MP_0009895)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009895
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Genes

10 gene mutations causing the decreased palatine bone horizontal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARID5B AT rich interactive domain 5B (MRF1-like)
CSRNP1 cysteine-serine-rich nuclear protein 1
EYA1 EYA transcriptional coactivator and phosphatase 1
MN1 meningioma (disrupted in balanced translocation) 1
RSPO2 R-spondin 2
SCHIP1 schwannomin interacting protein 1
SGPL1 sphingosine-1-phosphate lyase 1
TBX22 T-box 22
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
WDR19 WD repeat domain 19