absent occipital bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the bone at the lower, posterior part of the skull (Mammalian Phenotype Ontology, MP_0004440)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004440
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2 gene mutations causing the absent occipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
RUNX2 runt-related transcription factor 2
TGFB2 transforming growth factor, beta 2