fusion of atlas and occipital bones Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description union of elements of the atlas and the bone at the lower, posterior part of the skull into one structure (Mammalian Phenotype Ontology, MP_0010728)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010728
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8 gene mutations causing the fusion of atlas and occipital bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CBX2 chromobox homolog 2
CDX1 caudal type homeobox 1
FGFR1 fibroblast growth factor receptor 1
HOXD1 homeobox D1
HOXD3 homeobox D3
RARB retinoic acid receptor, beta
RARG retinoic acid receptor, gamma
TSHZ1 teashirt zinc finger homeobox 1