small basioccipital bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the bone in the base of the cranium, frequently forming a part of the occipital in the adult, but usually distinct in the young (Mammalian Phenotype Ontology, MP_0004447)
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7 gene mutations causing the small basioccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGFRL1 fibroblast growth factor receptor-like 1
HHAT hedgehog acyltransferase
LTBP1 latent transforming growth factor beta binding protein 1
NKX3-2 NK3 homeobox 2
SKI SKI proto-oncogene
TBX15 T-box 15
WNT9A wingless-type MMTV integration site family, member 9A