decreased cranium width Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description having a decreased side-to-side, or lateral distance of the cranium (Mammalian Phenotype Ontology, MP_0008526)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008526
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Genes

8 gene mutations causing the decreased cranium width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EIF4H eukaryotic translation initiation factor 4H
LMNA lamin A/C
MMP14 matrix metallopeptidase 14 (membrane-inserted)
NPR2 natriuretic peptide receptor 2
PC pyruvate carboxylase
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
SOSTDC1 sclerostin domain containing 1
TBX15 T-box 15