Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol MSX2 contributors: mct/npt/pgu - updated : 18-09-2015
HGNC name msh homeobox 2
HGNC id 7392
ANIMAL & CELL MODELS
  • defects in bone growth and ectodermal organ formation in Msx2 deficient mice, premature cranial suture closure
  • expression of the Msx2 homeobox gene, an essential regulator of calvarial bone development is absent in the skull mesenchymal progenitors of Foxc1 mutant mice
  • Msx1;Msx2 double mutants are characterized by the loss of derivatives of the anterior limb mesoderm which is not observed in either of the simple mutants