absent neurocranium Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing bones of the skull enclosing the brain (Mammalian Phenotype Ontology, MP_0000075)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000075
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Genes

5 gene mutations causing the absent neurocranium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
LAMA5 laminin, alpha 5
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
SCUBE1 signal peptide, CUB domain, EGF-like 1
SHROOM3 shroom family member 3