short premaxilla Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced length of the anterior and interior portion of the maxilla (Mammalian Phenotype Ontology, MP_0000091)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000091
Similar Terms
Downloads & Tools

Genes

12 gene mutations causing the short premaxilla 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
CREBBP CREB binding protein
DLX5 distal-less homeobox 5
FGF9 fibroblast growth factor 9
HRAS Harvey rat sarcoma viral oncogene homolog
PHEX phosphate regulating endopeptidase homolog, X-linked
SCHIP1 schwannomin interacting protein 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
ZEB1 zinc finger E-box binding homeobox 1
ZIC5 Zic family member 5