abnormal premaxilla morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the anterior and inner portion of the maxilla (Mammalian Phenotype Ontology, MP_0002820)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002820
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Genes

24 gene mutations causing the abnormal premaxilla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARID5B AT rich interactive domain 5B (MRF1-like)
BRD4 bromodomain containing 4
CDON cell adhesion associated, oncogene regulated
COL2A1 collagen, type II, alpha 1
CREBBP CREB binding protein
DLG1 discs, large homolog 1 (Drosophila)
DLX5 distal-less homeobox 5
DLX6 distal-less homeobox 6
EYA1 EYA transcriptional coactivator and phosphatase 1
FBLN1 fibulin 1
FGF9 fibroblast growth factor 9
FGFR3 fibroblast growth factor receptor 3
HRAS Harvey rat sarcoma viral oncogene homolog
MSX1 msh homeobox 1
NABP2 nucleic acid binding protein 2
PHEX phosphate regulating endopeptidase homolog, X-linked
SATB2 SATB homeobox 2
SCHIP1 schwannomin interacting protein 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
WDR19 WD repeat domain 19
ZEB1 zinc finger E-box binding homeobox 1
ZIC3 Zic family member 3
ZIC5 Zic family member 5